Gene list
Applied filters:
COG category: Intracellular trafficking and secretion
Number of genes found: 470
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium discoideum AX4, AX4 | ||||||||
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Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
DDB_G0267538 | DDB_G0267538 | DDB0232428 | CDS | 291771 | 1824 | + | 0.313596 | |
DDB_G0269942 | DDB_G0269942 | belongs to the synaptobrevin family ortholog of human SEC22B contains a longin domain and a v-snare coiled-coil domain contains 1 predicted transmembrane domain | DDB0232428 | CDS | 3911017 | 645 | + | 0.24031 |
DDB_G0271044 | DDB_G0271044 | contains Sec23Sec24 zinc finger trunk and helical domains yeast Sec23Sec24 is a component of COPII (coat protein complex II) involved in ER to Golgi transport | DDB0232428 | CDS | 4346844 | 2391 | - | 0.26056 |
DDB_G0272318 | DDB_G0272318 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) | DDB0232429 | CDS | 1278811 | 1551 | + | 0.350097 |
DDB_G0272594_ps | DDB_G0272594 | putative pseudogene very similar to the putative importin subunit alpha C gene | DDB0232429 | CDS | 2405347 | 747 | - | 0.293173 |
DDB_G0273149 | DDB_G0273149 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) there is a second copy of this gene | DDB0232429 | CDS | 2875789 | 1653 | - | 0.333333 |
DDB_G0273467 | DDB_G0273467 | there is a second copy of this gene | DDB0232429 | CDS | 2890795 | 429 | + | 0.2331 |
DDB_G0273579 | DDB_G0273579 | there is a second copy of this gene | DDB0232429 | CDS | 3140434 | 429 | - | 0.2331 |
DDB_G0273595 | DDB_G0273595 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) there is a second copy of this gene | DDB0232429 | CDS | 3154181 | 1653 | + | 0.333333 |
DDB_G0274789 | DDB_G0274789 | DDB0232429 | CDS | 3841237 | 6309 | + | 0.277223 | |
DDB_G0274813 | DDB_G0274813 | conserved protein mainly among fungi and plants | DDB0232429 | CDS | 3971713 | 2817 | + | 0.302449 |
DDB_G0275571 | DDB_G0275571 | DDB0232429 | CDS | 5522231 | 2793 | + | 0.3029 | |
DDB_G0275603 | DDB_G0275603 | DDB0232429 | CDS | 5583526 | 1782 | + | 0.319865 | |
DDB_G0275843 | DDB_G0275843 | DDB0232429 | CDS | 5657920 | 2226 | - | 0.310422 | |
DDB_G0276239 | DDB_G0276239 | involved in vesicle-mediated transport similar to VPS33 | DDB0232429 | CDS | 6373737 | 2577 | - | 0.217307 |
DDB_G0276625 | DDB_G0276625 | belongs to the drugmetabolite transporter superfamily similar to human SLC35D1 (UDP-glucuronic acidUDP-N-acetylgalactosamine transporter) and S. cerevisiae VRG4 (GDP-mannose transporter 1) contains 8 putative transmembrane domains | DDB0232429 | CDS | 7055459 | 945 | - | 0.271958 |
DDB_G0277537 | DDB_G0277537 | subunit of PI4K responsible for the phosphorylation of phosphatidylinositol (PI) to PI4P (ATP 1-phosphatidyl-1D-myo-inositol ADP 1-phosphatidyl-1D-myo-inositol 4-phosphate) the first committed step in the generation of phosphatidylinositol 45-bisphosphate (PIP2) a precursor of the second messenger inositol 145-trisphosphate (InsP3) | DDB0232429 | CDS | 7989159 | 7383 | + | 0.301233 |
DDB_G0277993 | DDB_G0277993 | importins function in nuclear protein import however this protein does not contain the N-terminal importin beta binding domain (IBB domain) | DDB0232430 | CDS | 126886 | 1575 | + | 0.31873 |
DDB_G0278143 | DDB_G0278143 | DDB0232430 | CDS | 347205 | 6408 | + | 0.302903 | |
DDB_G0278267 | DDB_G0278267 | DDB0232430 | CDS | 586381 | 2631 | + | 0.259597 | |
DDB_G0278333 | DDB_G0278333 | DDB0232430 | CDS | 713907 | 1950 | - | 0.315385 | |
DDB_G0278631 | DDB_G0278631 | putative ortholog of H. sapiens SLC35D2 UDP-N-acetylglucosamineUDP-glucoseGDP-mannose transporter contains 10 putative transmembrane domains | DDB0232430 | CDS | 462648 | 1149 | + | 0.222802 |
DDB_G0278773 | DDB_G0278773 | similar to human VAPA and VAPB defects in VAPB cause amyotrophic lateral sclerosis 8 (ALS8) | DDB0232430 | CDS | 1149897 | 933 | - | 0.276527 |
DDB_G0278973 | DDB_G0278973 | DDB0232430 | CDS | 1448552 | 1845 | - | 0.197832 | |
DDB_G0280525 | DDB_G0280525 | DDB0232430 | CDS | 3381127 | 4614 | + | 0.252492 | |
DDB_G0281627 | DDB_G0281627 | DDB0232430 | CDS | 4725130 | 1827 | + | 0.305419 | |
DDB_G0282017 | DDB_G0282017 | involved in vesicle-mediated transport similar to VPS33 | DDB0232430 | CDS | 5245886 | 1944 | + | 0.237654 |
DDB_G0283011 | DDB_G0283011 | DDB0232431 | CDS | 151994 | 360 | - | 0.286111 | |
DDB_G0284149 | DDB_G0284149 | ortholog of yeast VID24 a peripheral membrane protein located at Vid (vacuole import and degradation) vesicles | DDB0232431 | CDS | 1533705 | 699 | - | 0.296137 |
DDB_G0286479 | DDB_G0286479 | DDB0232431 | CDS | 4506469 | 3504 | - | 0.257991 | |
DDB_G0286695 | DDB_G0286695 | DDB0232431 | CDS | 4856852 | 735 | - | 0.285714 | |
DDB_G0288079_ps | DDB_G0288079 | similar to DDB_G0277993 a protein of the importin family | DDB0232432 | CDS | 1063770 | 1194 | - | 0.326633 |
DDB_G0288849 | DDB_G0288849 | contains a predicted signal peptide and a putative C-terminal transmembrane domain similar to S. cerevisiae ERO1 (endoplasmic oxidoreductin-1) which is required for the formation of disulfide bonds in the proteins in the endoplasmic reticulum | DDB0232432 | CDS | 2057527 | 1662 | - | 0.253309 |
DDB_G0290341 | DDB_G0290341 | similar to S. cerevisiae SFT2 contains 4 putative transmembrane domains similar to D. purpureum protein | DDB0232432 | CDS | 3989030 | 621 | - | 0.259259 |
DDB_G0291055 | DDB_G0291055 | homolog of human SFT2D1 (SFT2 domain-containing protein 1) contains 4 putative transmembrane domains | DDB0232432 | CDS | 4835830 | 477 | + | 0.295597 |
DDB_G0291406 | DDB_G0291406 | DDB0232433 | CDS | 260638 | 12408 | + | 0.230819 | |
DDB_G0292148 | DDB_G0292148 | DDB0232433 | CDS | 1273206 | 1569 | - | 0.262588 | |
DDB_G0293328 | DDB_G0293328 | DDB0232433 | CDS | 2760211 | 396 | + | 0.39899 | |
DDB_G0293622 | DDB_G0293622 | DDB0232433 | CDS | 3159608 | 2976 | + | 0.290995 | |
DDB_G0293712 | DDB_G0293712 | DDB0232433 | CDS | 3080260 | 564 | + | 0.281915 | |
acapA | DDB_G0279649 | plays a role in cytokinesis cell migration and actin cytoskeleton dynamics hydrolyzes GTP bound to ArfA in vitro | DDB0232430 | CDS | 2363863 | 4002 | + | 0.31959 |
acapB | DDB_G0276395 | similar to mammalian Acap3 hydrolyzes GTP bound to ArfA in vitro | DDB0232429 | CDS | 6763233 | 2532 | + | 0.265798 |
ap1b1 | DDB_G0279141 | highly similar to AP-1 complex subunit beta-1 (AP1B1) and AP-2 complex subunit beta-1 (AP2B1) which play a role in clathrin-dependent protein sorting | DDB0232430 | CDS | 1680228 | 2829 | - | 0.331212 |
ap1s1 | DDB_G0279359 | DDB0232430 | CDS | 1984933 | 471 | + | 0.26327 | |
ap1s2 | DDB_G0295711 | DDB0232433 | CDS | 619891 | 465 | - | 0.260215 | |
ap2s1 | DDB_G0289721 | DDB0232432 | CDS | 3163717 | 429 | - | 0.261072 | |
ap3b-1 | DDB_G0272578 | there is a second copy of this gene | DDB0232429 | CDS | 2374895 | 3327 | - | 0.285843 |
ap3b-2 | DDB_G0274003 | there is a second copy of this gene | DDB0232429 | CDS | 3652959 | 3327 | + | 0.285843 |
ap3s1 | DDB_G0275405 | DDB0232429 | CDS | 5412017 | 516 | - | 0.226744 | |
ap4b1 | DDB_G0283319 | putative ortholog of H. sapiens AP4B1 member of a complex that mediates protein sorting | DDB0232431 | CDS | 525048 | 2517 | + | 0.247517 |
ap4e1 | DDB_G0280427 | DDB0232430 | CDS | 3335352 | 3243 | - | 0.254702 | |
ap4s1 | DDB_G0284905 | DDB0232431 | CDS | 2625777 | 420 | - | 0.240476 | |
atr1 | DDB_G0291380 | atypical PIKK family protein kinase similar to protein kinase ATR which modulates cell cycle progression and DNA repair in other organisms ATR phosphorylates Rad17 histone H2AX p53 and Nbs1 | DDB0232433 | CDS | 214264 | 9474 | - | 0.259552 |
copB | DDB_G0284735 | beta subunit of the coatomer complex essential for the secretory pathway colocalizes with comitin at the Golgi | DDB0232431 | CDS | 2394561 | 2739 | + | 0.316174 |
copG | DDB_G0289371 | DDB0232432 | CDS | 2724036 | 2697 | + | 0.309974 | |
crsA | DDB_G0282607 | catalyzes the reaction acyl-CoA sphingosine CoA N-acylsphingosine in ceramide synthesis ortholog of S. cerevisiae LAG1 and H. sapiens TRH1 | DDB0232430 | CDS | 5996864 | 1026 | - | 0.273879 |
dnapkcs | DDB_G0281167 | atypical PIKK family protein kinase similar to human DNA-PKcs required for the repair of DNA double-strand breaks belongs to the PIKK family of protein kinases | DDB0232430 | CDS | 4132807 | 12900 | + | 0.265504 |
exoc3 | DDB_G0293520 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232433 | CDS | 2981805 | 2352 | + | 0.274235 |
gacC | DDB_G0284571 | DDB0232431 | CDS | 2170033 | 1200 | - | 0.288333 | |
golt1 | DDB_G0292868 | conserved protein might be involved in fusion of ER-derived transport vesicles with the Golgi complex | DDB0232433 | CDS | 2183910 | 417 | - | 0.270983 |
grpA | DDB_G0293248 | involved in the unconventional secretory pathway of acbA the precurser of SDF-2 (spore differentiation factor 2) ortholog of the mammalian golgi reassembly stacking protein 2 (golgi reassembly-stacking protein of 55 kDa) | DDB0232433 | CDS | 2631684 | 984 | + | 0.311992 |
gxcDD | DDB_G0279733 | multifunctional protein containing a Rac exchange factor domain an Arf GTPase activating domain a CH domain two IQ motifs and three PH domains | DDB0232430 | CDS | 2433796 | 9348 | + | 0.295892 |
immp | DDB_G0283049 | in other organisms there are two subunits for this enzyme with relatively high sequence similarity to each other Dictyostelium appear to have a single gene | DDB0232431 | CDS | 142399 | 972 | + | 0.220165 |
kdelr | DDB_G0272124 | endoplasmic reticulum receptor for the KDEL signal sequence of proteins resident in the endoplasmic reticulum believed to cycle between the cis side of the Golgi apparatus and the ER | DDB0232429 | CDS | 1376821 | 657 | - | 0.25723 |
nup155 | DDB_G0291163 | component of the nuclear pore complex may be involved both in binding and translocating proteins | DDB0232432 | CDS | 5077769 | 4728 | - | 0.271151 |
oxaA | DDB_G0284883 | similar to OXA1 a conserved inner mitochondrial membrane protein that is required for the activity and assembly of cytochrome oxidase and for the insertion of integral membrane proteins into the mitochondrial inner membrane there is a second putative oxidase assembly protein in D. discoideum | DDB0232431 | CDS | 2586982 | 1191 | + | 0.260285 |
oxaB | DDB_G0281171 | similar to OXA1 a conserved inner mitochondrial membrane protein that is required for the activity and assembly of cytochrome oxidase and for the insertion of integral membrane proteins into the mitochondrial inner membrane there is a second putative oxidase assembly protein in D. discoideum | DDB0232430 | CDS | 4148918 | 1257 | - | 0.275259 |
pex5 | DDB_G0286033 | ortholog of peroxin 5 peroxisomal membrane signal receptor for C-terminal tripeptide signal sequence (PTS1) of peroxisomal matrix proteins required for peroxisomal matrix protein importmutations in human homolog cause a variety of peroxisomal disorders | DDB0232431 | CDS | 3973237 | 1926 | - | 0.336449 |
pikA | DDB_G0278727 | DDB0232430 | CDS | 1154369 | 4716 | + | 0.261026 | |
pikB | DDB_G0283081 | DDB0232431 | CDS | 247398 | 5574 | - | 0.311805 | |
pikC | DDB_G0275011 | DDB0232429 | CDS | 5211773 | 5094 | + | 0.270907 | |
pikD | DDB_G0288485 | subunit of PI4K responsible for the phosphorylation of phosphatidylinositol (PI) to PI4P (ATP 1-phosphatidyl-1D-myo-inositol ADP 1-phosphatidyl-1D-myo-inositol 4-phosphate) the first committed step in the generation of phosphatidylinositol 45-bisphosphate (PIP2) a precursor of the second messenger inositol 145-trisphosphate (InsP3) | DDB0232432 | CDS | 1616073 | 3543 | + | 0.269828 |
pikE | DDB_G0289601 | ortholog of yeast VPS34 a phosphatidylinositol 3-kinase | DDB0232432 | CDS | 3005109 | 2451 | - | 0.299878 |
pikF | DDB_G0268548 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | DDB0232428 | CDS | 1099622 | 4149 | + | 0.291396 |
pikG | DDB_G0282625 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | DDB0232430 | CDS | 6013022 | 5016 | - | 0.234649 |
pikH | DDB_G0291093 | putative PI3k putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring unlike other PI3Ks does not contain a ras binding domain but a PH domain and does not localize to the cell cortex upon chemotactic stimulation | DDB0232432 | CDS | 4980832 | 5463 | - | 0.242541 |
prafA | DDB_G0278887 | belongs to a conserved family of multi-pass transmembrane proteins contains 3 predicted transmembrane domains | DDB0232430 | CDS | 1342274 | 708 | - | 0.303672 |
ranbp1 | DDB_G0287391 | DDB0232432 | CDS | 246455 | 585 | + | 0.353846 | |
rer1 | DDB_G0292588 | conserved protein involved in the retrieval of some endoplasmic reticulum membrane proteins from the early golgi compartment contains 3 predicted transmembrane domains | DDB0232433 | CDS | 1815723 | 567 | - | 0.292769 |
scfd1 | DDB_G0288719 | DDB0232432 | CDS | 1870694 | 2022 | - | 0.271019 | |
sec1 | DDB_G0283937 | highly similar to mammalian Sec1 (also known as syntaxin binding protein 1) which plays a role in vesicle transport by binding to t-SNAREs expressed in prespore cells involved in osmoregulation and hence cell motility | DDB0232431 | CDS | 1335851 | 1797 | + | 0.329994 |
sec23 | DDB_G0281985 | DDB0232430 | CDS | 5216752 | 2253 | + | 0.376831 | |
sec24 | DDB_G0281255 | DDB0232430 | CDS | 4298212 | 3042 | + | 0.359303 | |
sec24l | DDB_G0277797 | component of COPII (coat protein complex II) involved in ER to Golgi transport similar to SEC24C and SEC24D | DDB0232429 | CDS | 8422539 | 3402 | + | 0.357731 |
sec61a | DDB_G0278885 | alpha subunit of the SEC61 complex (composed of | DDB0232430 | CDS | 1338636 | 1428 | - | 0.366947 |
sec61g | DDB_G0287777 | gamma subunit of the SEC61 complex (composed of | DDB0232432 | CDS | 682723 | 210 | + | 0.328571 |
sec63 | DDB_G0286131 | similar to the widely conserved SEC63 which seems to be required for integral membrane and secreted preprotein translocation across the endoplasmic reticulum membrane | DDB0232431 | CDS | 4064803 | 2445 | - | 0.350102 |
smg1 | DDB_G0275845 | atypical PIKK family protein kinase similar to the PI-3-kinase-related kinase SMG1 which functions in nonsense-mediated mRNA decay belongs to the PIKK family of protein kinases | DDB0232429 | CDS | 5665840 | 7035 | + | 0.267235 |
srp19 | DDB_G0275211 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232429 | CDS | 5011473 | 537 | + | 0.312849 |
srp54 | DDB_G0275455 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232429 | CDS | 6110111 | 1629 | - | 0.361572 |
srpR | DDB_G0277377 | DDB0232429 | CDS | 7920699 | 1848 | - | 0.308983 | |
syn16A | DDB_G0276575 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232429 | CDS | 6993306 | 945 | + | 0.256085 |
syn16B | DDB_G0276469 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232429 | CDS | 6988936 | 1008 | + | 0.249008 |
syn1A | DDB_G0289379 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232432 | CDS | 2678322 | 1002 | - | 0.297405 |
syn1B | DDB_G0270556 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | DDB0232428 | CDS | 2999912 | 1005 | + | 0.250746 |
syn7A | DDB_G0287733 | member of the SNARE family (Soluble NSF Attachment Protein REceptor) plays a role in endosomal fusion | DDB0232432 | CDS | 617723 | 1071 | + | 0.289449 |
tipC | DDB_G0267422 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention in D. discoideum involved in early development and tip formation | DDB0232428 | CDS | 1494431 | 11547 | + | 0.250108 |
tnpo | DDB_G0269948 | homolog of H. sapiens TNPO12 and S. cervisiae KAP104 (karyopherin 104) involved in nuclear protein import | DDB0232428 | CDS | 3916816 | 2796 | + | 0.327253 |
tor | DDB_G0281569 | atypical PIKK family FRAP subfamily protein kinase ortholog of tor a protein kinase that plays a central role in response to nutrients stress and intracellular energy state called mTOR in mammals in dTOR in Drosophila | DDB0232430 | CDS | 4934791 | 7143 | - | 0.347893 |
trappc4 | DDB_G0280827 | ortholog of the trafficking protein particle complex subunit 4 part of the multisubunit TRAPP (transport protein particle) complex | DDB0232430 | CDS | 1440057 | 408 | - | 0.272059 |
trappc5 | DDB_G0278643 | homolog of human TRAPPC5 a component of the multisubunit TRAPP (transport protein particle) complex which may play a role in vesicular transport from endoplasmic reticulum to Golgi | DDB0232430 | CDS | 551038 | 561 | + | 0.286988 |
vamp7A | DDB_G0284951 | member of the SNARE family (Soluble NSF Attachment Protein REceptor) localizes to endosome and interacts with syn7A | DDB0232431 | CDS | 2678890 | 651 | + | 0.288786 |
vamp7B | DDB_G0277173 | SNARE protein interacts with AP180 (clmA) which retrieves Vamp7B from the contractile vacuole | DDB0232429 | CDS | 7680323 | 783 | + | 0.297573 |
vps13A | DDB_G0286725 | putative ortholog of S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 4889609 | 10122 | - | 0.30488 |
vps13B | DDB_G0274917 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232429 | CDS | 4457216 | 18186 | - | 0.252777 |
vps13D | DDB_G0286545 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 4616198 | 13779 | - | 0.252994 |
vps13E | DDB_G0268886 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232428 | CDS | 2311232 | 12726 | + | 0.274399 |
vps13F | DDB_G0287055 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DDB0232431 | CDS | 5237174 | 12741 | - | 0.271172 |
vps33 | DDB_G0291097 | DDB0232432 | CDS | 4992025 | 1935 | - | 0.328165 | |
vps45 | DDB_G0290213 | putative ortholog of VPS45 involved in vacuolar protein sorting | DDB0232432 | CDS | 3802462 | 1692 | - | 0.278369 |
vps5 | DDB_G0272989 | putative ortholog of mammalian sorting nexin and S. cerevisiae VPS5 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | DDB0232429 | CDS | 2025586 | 1638 | - | 0.339438 |
xpo1 | DDB_G0291306 | DDB0232433 | CDS | 102439 | 3174 | - | 0.3431 | |
xpo5 | DDB_G0284379 | DDB0232431 | CDS | 1912156 | 3408 | - | 0.289319 | |
yipf5 | DDB_G0283541 | very similar to Yip1 domain family member 5 (YIPF5) in yeast YIP1 localizes to the Golgi and interacts with GTPases contains four putative transmembrane domains | DDB0232431 | CDS | 791068 | 639 | + | 0.273865 |
yipf6 | DDB_G0282825 | very similar to Yip1 domain family member 6 (YIPF6) in yeast YIP1 localizes to the Golgi and interacts with GTPases contains five putative transmembrane domains | DDB0232430 | CDS | 6266209 | 549 | - | 0.300546 |
ykt6 | DDB_G0291656 | DDB0232433 | CDS | 180176 | 609 | + | 0.320197 | |
Dictyostelium fasciculatum, SH3 | ||||||||
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g1011 | DFA_01002 | Dfasci-F-a-25c12.r2-5 | CDS | 1718077 | 2295 | - | 0.415686 | |
g10215 | DFA_13286 | EU5ZYIE02H8LDV-5 | CDS | 1890012 | 429 | - | 0.27972 | |
g10218 | DFA_10622 | EU5ZYIE02H8LDV-5 | CDS | 1894158 | 4194 | - | 0.399142 | |
g10264 | DFA_10668 | EUAJFUG01CK1KI-5 | CDS | 118441 | 2433 | - | 0.311139 | |
g10485 | DFA_10901 | EUAJFUG02G6ADK-5 | CDS | 100084 | 2481 | + | 0.411931 | |
g1059 | DFA_01049 | Dfasci-F-a-25c12.r2-5 | CDS | 1835263 | 5838 | + | 0.341555 | |
g10664 | DFA_13322 | EUAJFUG02HR96I-5 | CDS | 146612 | 1659 | - | 0.324292 | |
g10728 | DFA_11142 | EUAJFUG02HR96I-5 | CDS | 332285 | 3660 | + | 0.437978 | |
g1084 | DFA_01074 | Dfasci-F-a-25c12.r2-5 | CDS | 1897832 | 2826 | + | 0.387827 | |
g10955 | DFA_11370 | EUAJFUG02HR96I-5 | CDS | 963832 | 2823 | - | 0.43429 | |
g10987 | DFA_11404 | EUAJFUG02HR96I-5 | CDS | 1033138 | 1821 | - | 0.392092 | |
g10994 | DFA_11412 | EUAJFUG02HR96I-5 | CDS | 1050472 | 12909 | - | 0.37989 | |
g11063 | DFA_11484 | EUAJFUG02HR96I-5 | CDS | 1225692 | 2016 | - | 0.351687 | |
g11120 | DFA_11543 | EUAJFUG02HR96I-5 | CDS | 1371566 | 1002 | + | 0.366267 | |
g11187 | DFA_11607 | EUAJFUG02HR96I-5 | CDS | 1542268 | 567 | - | 0.345679 | |
g11271 | DFA_11691 | EUAJFUG02HR96I-5 | CDS | 1760384 | 5535 | + | 0.334959 | |
g1136 | DFA_01131 | Dfasci-F-a-25c12.r2-5 | CDS | 2036090 | 3039 | + | 0.350115 | |
g11375 | DFA_11807 | EUAJFUG02HR96I-5 | CDS | 2055701 | 1443 | + | 0.335412 | |
g11405 | DFA_13390 | EUAJFUG02HR96I-5 | CDS | 2140527 | 3918 | + | 0.412966 | |
g11439 | DFA_11886 | EUAJFUG02HR96I-5 | CDS | 2237564 | 4419 | - | 0.379498 | |
g11459 | DFA_11912 | EUAJFUG02HR96I-5 | CDS | 2298761 | 2466 | + | 0.315085 | |
g11467 | DFA_11920 | EUAJFUG02HR96I-5 | CDS | 2322328 | 2298 | + | 0.363795 | |
g11492 | DFA_11951 | EUAJFUG02HR96I-5 | CDS | 2385724 | 453 | + | 0.441501 | |
g11508 | DFA_11968 | EUAJFUG02HR96I-5 | CDS | 2424110 | 2862 | + | 0.283718 | |
g11566 | DFA_12028 | EUAJFUG02HR96I-5 | CDS | 2554480 | 1683 | - | 0.458705 | |
g11591 | DFA_12052 | EUAJFUG02HR96I-5 | CDS | 2631222 | 1857 | + | 0.315563 | |
g1183 | DFA_01181 | Dfasci-F-a-25c12.r2-5 | CDS | 2142159 | 924 | - | 0.310606 | |
g11838 | DFA_12320 | EUAJFUG02HR96I-5 | CDS | 3294799 | 3405 | - | 0.424082 | |
g1321 | DFA_01321 | Dfasci-F-a-25c12.r2-5 | CDS | 2475311 | 765 | - | 0.320261 | |
g1346 | DFA_01349 | Dfasci-F-a-25c12.r2-5 | CDS | 2531976 | 2220 | + | 0.333784 | |
g1445 | DFA_01447 | Dfasci-F-a-25c12.r2-5 | CDS | 2762553 | 1266 | - | 0.390205 | |
g1576 | DFA_01581 | Dfasci-F-a-25c12.r2-5 | CDS | 3099904 | 3147 | + | 0.370512 | |
g1624 | DFA_01638 | Dfasci-F-a-25c12.r2-5 | CDS | 3238344 | 885 | - | 0.322034 | |
g1668 | DFA_01680 | Dfasci-F-a-25c12.r2-5 | CDS | 3353359 | 876 | + | 0.400685 | |
g1871 | DFA_01898 | Dfasci-F-a-25c12.r2-5 | CDS | 3905185 | 1950 | + | 0.386154 | |
g2013 | DFA_02046 | Dfasci-G-b-126g04.f1-5 | CDS | 90745 | 426 | + | 0.323944 | |
g2089 | DFA_02132 | Dfasci-G-b-126g04.f1-5 | CDS | 286561 | 8835 | - | 0.405207 | |
g2162 | DFA_02213 | Dfasci-G-b-143d02.r1-5 | CDS | 5380 | 4494 | + | 0.32866 | |
g2307 | DFA_02356 | Dfasci-G-b-143d02.r1-5 | CDS | 370463 | 1506 | - | 0.298805 | |
g2468 | DFA_02518 | Dfasci-G-b-190b03.r1-5 | CDS | 105762 | 3459 | - | 0.336513 | |
g2735 | DFA_02787 | Dfasci-G-b-205a01.r1-3 | CDS | 216359 | 4713 | - | 0.398472 | |
g2744 | DFA_02798 | Dfasci-G-b-205a01.r1-3 | CDS | 247026 | 3150 | - | 0.424127 | |
g2897 | DFA_02964 | Dfasci-G-b-205a01.r1-3 | CDS | 648666 | 1062 | + | 0.311676 | |
g304 | DFA_00293 | Dfasci-F-a-11f03.f1-5 | CDS | 839733 | 1806 | - | 0.365449 | |
g3100 | DFA_03185 | Dfasci-G-b-205a01.r1-3 | CDS | 1179186 | 2262 | + | 0.454023 | |
g3123 | DFA_03210 | Dfasci-G-b-205a01.r1-3 | CDS | 1240716 | 5160 | - | 0.327713 | |
g3132 | DFA_03221 | Dfasci-G-b-205a01.r1-3 | CDS | 1273744 | 1959 | - | 0.48392 | |
g3350 | DFA_03451 | Dfasci-G-b-205a01.r1-3 | CDS | 1862856 | 16128 | - | 0.399368 | |
g3462 | DFA_03576 | Dfasci-G-b-205a01.r1-3 | CDS | 2220757 | 465 | - | 0.309677 | |
g3585 | DFA_03702 | Dfasci-G-b-285a01.f1-5 | CDS | 66178 | 2193 | + | 0.416781 | |
g3683 | DFA_03816 | Dfasci-G-b-285a01.f1-5 | CDS | 329855 | 612 | + | 0.289216 | |
g4038 | DFA_04204 | Dfasci-G-b-285a01.f1-5 | CDS | 1246920 | 2511 | - | 0.360812 | |
g4042 | DFA_04207 | Dfasci-G-b-285a01.f1-5 | CDS | 1257679 | 636 | - | 0.279874 | |
g4081 | DFA_04241 | Dfasci-G-o-33e01.r1-3 | CDS | 18604 | 2745 | - | 0.34827 | |
g4082 | DFA_04242 | Dfasci-G-o-33e01.r1-3 | CDS | 22114 | 12666 | - | 0.353466 | |
g4134 | DFA_04294 | Dfasci-G-o-33e01.r1-3 | CDS | 168845 | 1644 | + | 0.45073 | |
g4456 | DFA_12783 | Dfasci-G-o-33e01.r1-3 | CDS | 978131 | 1524 | + | 0.295932 | |
g4458 | DFA_04618 | Dfasci-G-o-33e01.r1-3 | CDS | 987054 | 1152 | - | 0.358507 | |
g4661 | DFA_04827 | Dfasci-G-o-80e12.f1-5 | CDS | 32367 | 1830 | + | 0.364481 | |
g4860 | DFA_05038 | Dfasci-G-o-80e12.f1-5 | CDS | 538613 | 1614 | + | 0.381041 | |
g4951 | DFA_05135 | Dfasci-G-o-80e12.f1-5 | CDS | 770448 | 1596 | + | 0.409148 | |
g4953 | DFA_05138 | Dfasci-G-o-80e12.f1-5 | CDS | 778085 | 1506 | - | 0.390438 | |
g5073 | DFA_05279 | Dfasci-G-o-80e12.f1-5 | CDS | 1136259 | 2562 | - | 0.456674 | |
g5216 | DFA_05421 | Dfasci-G-o-80e12.f1-5 | CDS | 1509187 | 498 | - | 0.331325 | |
g5526 | DFA_05738 | Dfasci-G-o-80e12.f1-5 | CDS | 2349625 | 705 | + | 0.408511 | |
g5581 | DFA_05791 | Dfasci-G-o-80e12.f1-5 | CDS | 2481664 | 8331 | - | 0.350618 | |
g5591 | DFA_05801 | Dfasci-G-o-80e12.f1-5 | CDS | 2504072 | 2670 | - | 0.370412 | |
g5712 | DFA_05917 | Dfasci-G-p-12c09.r1-3 | CDS | 64759 | 504 | + | 0.321429 | |
g5713 | DFA_05918 | Dfasci-G-p-12c09.r1-3 | CDS | 66052 | 10704 | + | 0.369395 | |
g5897 | DFA_06109 | Dfasci-G-p-12c09.r1-3 | CDS | 530985 | 3294 | - | 0.376746 | |
g5914 | DFA_06131 | Dfasci-G-p-12c09.r1-3 | CDS | 591740 | 12291 | + | 0.432674 | |
g5975 | DFA_06196 | Dfasci-G-p-12c09.r1-3 | CDS | 749346 | 3873 | + | 0.394268 | |
g6085 | DFA_06324 | Dfasci-G-p-12c09.r1-3 | CDS | 1036520 | 3003 | - | 0.325008 | |
g6116 | DFA_06359 | Dfasci-G-p-12c09.r1-3 | CDS | 1125145 | 2847 | + | 0.372322 | |
g6201 | DFA_06443 | Dfasci-G-p-12c09.r1-3 | CDS | 1344810 | 6663 | - | 0.396068 | |
g622 | DFA_00605 | Dfasci-F-a-25c12.r2-5 | CDS | 700840 | 2970 | + | 0.394276 | |
g6594 | DFA_06855 | ET2XIPL01CNAVH-3 | CDS | 19348 | 11259 | + | 0.348876 | |
g6830 | DFA_07097 | ET2XIPL01CNAVH-3 | CDS | 641887 | 567 | - | 0.312169 | |
g6866 | DFA_07137 | ET2XIPL01CNAVH-3 | CDS | 744060 | 6906 | + | 0.398349 | |
g698 | DFA_00682 | Dfasci-F-a-25c12.r2-5 | CDS | 907240 | 4410 | + | 0.339683 | |
g6996 | DFA_07269 | ET2XIPL01CNAVH-3 | CDS | 1083042 | 1731 | - | 0.402657 | |
g7177 | DFA_07448 | ET2XIPL01CNAVH-3 | CDS | 1541344 | 3096 | - | 0.312984 | |
g7267 | DFA_07536 | ET2XIPL01CNAVH-3 | CDS | 1780126 | 1953 | + | 0.334357 | |
g7461 | DFA_07719 | ET2XIPL01COFD4-5 | CDS | 380286 | 1074 | - | 0.402235 | |
g7537 | DFA_07798 | ET2XIPL01COFD4-5 | CDS | 563666 | 3165 | - | 0.384834 | |
g7539 | DFA_07800 | ET2XIPL01COFD4-5 | CDS | 571439 | 606 | - | 0.438944 | |
g7803 | DFA_08077 | ET2XIPL01COFD4-5 | CDS | 1197548 | 2553 | - | 0.343126 | |
g7851 | DFA_08130 | ET2XIPL01COFD4-5 | CDS | 1335185 | 2424 | - | 0.304868 | |
g7945 | DFA_08234 | ET2XIPL01COFD4-5 | CDS | 1576085 | 942 | + | 0.368365 | |
g7972 | DFA_08267 | ET2XIPL01COFD4-5 | CDS | 1647245 | 1422 | + | 0.449367 | |
g813 | DFA_00803 | Dfasci-F-a-25c12.r2-5 | CDS | 1225401 | 2496 | - | 0.333734 | |
g814 | DFA_00805 | Dfasci-F-a-25c12.r2-5 | CDS | 1228489 | 9030 | - | 0.314618 | |
g8201 | DFA_13109 | ET2XIPL01COFD4-5 | CDS | 2307752 | 651 | - | 0.356375 | |
g8244 | DFA_08542 | ET2XIPL01COFD4-5 | CDS | 2413115 | 2280 | - | 0.370175 | |
g841 | DFA_00832 | Dfasci-F-a-25c12.r2-5 | CDS | 1290026 | 9633 | - | 0.415343 | |
g8448 | DFA_08750 | ET2XIPL01COFD4-5 | CDS | 2960909 | 435 | + | 0.296552 | |
g8472 | DFA_08772 | ET2XIPL01COFD4-5 | CDS | 3009762 | 6645 | - | 0.399097 | |
g8480 | DFA_08783 | ET2XIPL01COFD4-5 | CDS | 3037613 | 2955 | - | 0.378342 | |
g8494 | DFA_08795 | ET2XIPL01COFD4-5 | CDS | 3071474 | 1563 | + | 0.383877 | |
g8539 | DFA_08844 | ET2XIPL01COFD4-5 | CDS | 3209165 | 663 | - | 0.334842 | |
g8874 | DFA_09195 | EU5ZYIE01DZOHE-5 | CDS | 115108 | 2943 | + | 0.360516 | |
g8957 | DFA_09277 | EU5ZYIE01DZOHE-5 | CDS | 336137 | 795 | + | 0.320755 | |
g8996 | DFA_09313 | EU5ZYIE01DZOHE-5 | CDS | 426709 | 1572 | + | 0.416031 | |
g9018 | DFA_09338 | EU5ZYIE01DZOHE-5 | CDS | 491468 | 1221 | + | 0.332514 | |
g9126 | DFA_09459 | EU5ZYIE01EUG8B-5 | CDS | 4798 | 3429 | + | 0.30417 | |
g9284 | DFA_09635 | EU5ZYIE01EUG8B-5 | CDS | 472103 | 441 | + | 0.324263 | |
g9328 | DFA_09678 | EU5ZYIE01EUG8B-5 | CDS | 587948 | 825 | + | 0.356364 | |
g9407 | DFA_09762 | EU5ZYIE01EUG8B-5 | CDS | 847855 | 1788 | + | 0.355705 | |
g9448 | DFA_09804 | EU5ZYIE02H8LDV-5 | CDS | 12491 | 3744 | + | 0.348825 | |
g9461 | DFA_09817 | EU5ZYIE02H8LDV-5 | CDS | 39797 | 414 | + | 0.362319 | |
g9572 | DFA_13232 | EU5ZYIE02H8LDV-5 | CDS | 326406 | 2778 | - | 0.391289 | |
g9575 | DFA_09930 | EU5ZYIE02H8LDV-5 | CDS | 335525 | 558 | - | 0.362007 | |
g9622 | DFA_09983 | EU5ZYIE02H8LDV-5 | CDS | 442628 | 7098 | - | 0.404057 | |
g9705 | DFA_10074 | EU5ZYIE02H8LDV-5 | CDS | 664717 | 1647 | + | 0.312083 | |
g9771 | DFA_10146 | EU5ZYIE02H8LDV-5 | CDS | 829527 | 678 | - | 0.321534 | |
g9847 | DFA_10225 | EU5ZYIE02H8LDV-5 | CDS | 1020201 | 4944 | + | 0.397856 | |
g9850 | DFA_10228 | EU5ZYIE02H8LDV-5 | CDS | 1029297 | 411 | - | 0.284672 | |
g9896 | DFA_10278 | EU5ZYIE02H8LDV-5 | CDS | 1132840 | 207 | + | 0.36715 | |
g9996 | DFA_10381 | EU5ZYIE02H8LDV-5 | CDS | 1362239 | 3723 | + | 0.45098 | |
Dictyostelium lacteum | ||||||||
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g10068 | DLA_11239 | GLQOFTK02JL55Q | CDS | 744417 | 1392 | + | 0.34842 | |
g10121 | DLA_11301 | GLQOFTK02JL55Q | CDS | 861962 | 600 | - | 0.32 | |
g10131 | DLA_11314 | GLQOFTK02JL55Q | CDS | 883525 | 1353 | - | 0.316334 | |
g10184 | DLA_11379 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) there is a second copy of this gene | GLQOFTK02JL55Q | CDS | 1021400 | 1650 | + | 0.330909 |
g10209 | DLA_11406 | newcontig00824_1.exp | CDS | 21406 | 1950 | - | 0.316923 | |
g1346 | DLA_01475 | F4PJNLW01B0TO9 | CDS | 131246 | 558 | + | 0.306452 | |
g1431 | DLA_01571 | F4PJNLW01B0TO9 | CDS | 311263 | 1335 | - | 0.28764 | |
g1493 | DLA_01638 | F4PJNLW01B0TO9 | CDS | 445215 | 936 | + | 0.356838 | |
g1564 | DLA_01716 | F4PJNLW01B0TO9 | CDS | 618733 | 624 | + | 0.301282 | |
g1640 | DLA_01795 | F4PJNLW01B0TO9 | CDS | 777633 | 1689 | - | 0.316163 | |
g1804 | DLA_11505 | F4PJNLW01C9MXC | CDS | 95206 | 1290 | - | 0.306202 | |
g188 | DLA_00213 | contig05409_1.exp | CDS | 431852 | 564 | + | 0.296099 | |
g2054 | DLA_02259 | F4PJNLW01DERRH | CDS | 398942 | 468 | - | 0.260684 | |
g2235 | DLA_02469 | F4PJNLW01EE5MJ | CDS | 78419 | 2289 | - | 0.351682 | |
g2251 | DLA_02488 | F4PJNLW01EE5MJ | CDS | 109636 | 4569 | + | 0.33968 | |
g2357 | DLA_02607 | F4PJNLW01EE5MJ | CDS | 354640 | 645 | - | 0.339535 | |
g2366 | DLA_02616 | F4PJNLW01EE5MJ | CDS | 373247 | 591 | + | 0.279188 | |
g2458 | DLA_02727 | F4PJNLW01EE5MJ | CDS | 588955 | 3414 | - | 0.347393 | |
g2481 | DLA_02752 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | F4PJNLW01EE5MJ | CDS | 642626 | 11559 | + | 0.33541 |
g2488 | DLA_02759 | F4PJNLW01EE5MJ | CDS | 667342 | 6816 | + | 0.359008 | |
g2591 | DLA_02874 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | F4PJNLW01EE5MJ | CDS | 898216 | 14703 | - | 0.327484 |
g2606 | DLA_02891 | contains Sec23Sec24 zinc finger trunk and helical domains yeast Sec23Sec24 is a component of COPII (coat protein complex II) involved in ER to Golgi transport | F4PJNLW01EE5MJ | CDS | 943766 | 2277 | + | 0.317523 |
g2708 | DLA_03003 | endoplasmic reticulum receptor for the KDEL signal sequence of proteins resident in the endoplasmic reticulum believed to cycle between the cis side of the Golgi apparatus and the ER | F4PJNLW01EE5MJ | CDS | 1143920 | 663 | + | 0.266968 |
g2724 | DLA_03020 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | F4PJNLW01EE5MJ | CDS | 1181808 | 477 | + | 0.333333 |
g2779 | DLA_03076 | F4PJNLW02GJ9ZB | CDS | 56201 | 2220 | - | 0.340991 | |
g2824 | DLA_03127 | F4PJNLW02GJ9ZB | CDS | 146833 | 2541 | - | 0.245179 | |
g2853 | DLA_03160 | F4PJNLW02GJ9ZB | CDS | 213172 | 4545 | + | 0.256106 | |
g2871 | DLA_03182 | F4PJNLW02GJ9ZB | CDS | 266560 | 510 | + | 0.235294 | |
g2942 | DLA_03260 | F4PJNLW02HBBIY | CDS | 138381 | 11952 | + | 0.347808 | |
g3021 | DLA_03347 | F4PJNLW02HBBIY | CDS | 321833 | 1110 | + | 0.341441 | |
g3156 | DLA_03498 | GAOABQK02FRRQV | CDS | 39437 | 1425 | - | 0.30386 | |
g3207 | DLA_03555 | GAOABQK02FWKR3 | CDS | 17848 | 1452 | - | 0.278926 | |
g3316 | DLA_03667 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GAOABQK02G6SYV | CDS | 194474 | 921 | + | 0.324647 |
g3329 | DLA_03680 | GAOABQK02G6SYV | CDS | 221699 | 456 | - | 0.29386 | |
g3336 | DLA_03689 | GAOABQK02G6SYV | CDS | 231693 | 1032 | - | 0.304264 | |
g3395 | DLA_03755 | GAOABQK02G6SYV | CDS | 363597 | 558 | + | 0.320789 | |
g344 | DLA_00386 | contig05409_1.exp | CDS | 787271 | 429 | + | 0.379953 | |
g359 | DLA_00401 | contig05409_1.exp | CDS | 830609 | 1770 | - | 0.337853 | |
g3782 | DLA_04192 | GAOABQK02G7M1S | CDS | 559788 | 3381 | - | 0.359065 | |
g3807 | DLA_04222 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | GAOABQK02G7M1S | CDS | 617133 | 4275 | - | 0.349942 |
g3816 | DLA_04233 | GAOABQK02G7M1S | CDS | 656435 | 1044 | - | 0.304598 | |
g3851 | DLA_04271 | GAOABQK02G7M1S | CDS | 737197 | 1590 | + | 0.267925 | |
g4130 | DLA_04578 | belongs to the synaptobrevin family ortholog of human SEC22B contains a longin domain and a v-snare coiled-coil domain contains 1 predicted transmembrane domain | GAOABQK02GQAQJ | CDS | 570431 | 627 | - | 0.283892 |
g4157 | DLA_04604 | GAOABQK02GQAQJ | CDS | 627845 | 1929 | + | 0.365993 | |
g4267 | DLA_04713 | GAOABQK02GQAQJ | CDS | 860607 | 1854 | - | 0.340345 | |
g4555 | DLA_05048 | GAOABQK02H81I9 | CDS | 262440 | 1518 | - | 0.373518 | |
g4596 | DLA_05090 | GAOABQK02H81I9 | CDS | 352560 | 1077 | - | 0.312906 | |
g4680 | DLA_05181 | GAOABQK02H81I9 | CDS | 553088 | 1659 | + | 0.335744 | |
g4800 | DLA_05313 | GAOABQK02H81I9 | CDS | 839363 | 3039 | - | 0.336624 | |
g4830 | DLA_05348 | GAOABQK02HUB3S | CDS | 11346 | 1809 | - | 0.319514 | |
g486 | DLA_00538 | contig05409_1.exp | CDS | 1115144 | 207 | - | 0.338164 | |
g5070 | DLA_05615 | GAOABQK02HUB3S | CDS | 553749 | 6030 | - | 0.315091 | |
g5085 | DLA_05630 | GAOABQK02HUB3S | CDS | 588330 | 2022 | - | 0.333828 | |
g5285 | DLA_05866 | GAOABQK02HUB3S | CDS | 1120661 | 2448 | - | 0.330474 | |
g5598 | DLA_06243 | GAOABQK02HUB3S | CDS | 1842440 | 417 | - | 0.270983 | |
g5662 | DLA_06308 | GAOABQK02IBA3P | CDS | 127226 | 600 | + | 0.343333 | |
g572 | DLA_00632 | contig05409_1.exp | CDS | 1311038 | 1035 | - | 0.296618 | |
g5739 | DLA_06401 | GAOABQK02IBA3P | CDS | 327191 | 3069 | - | 0.358749 | |
g5952 | DLA_06631 | GAOABQK02IBA3P | CDS | 824711 | 705 | - | 0.307801 | |
g6112 | DLA_06805 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) | GAOABQK02IO52T | CDS | 49054 | 1587 | + | 0.360428 |
g632 | DLA_00700 | F4PJNLW01A00V1 | CDS | 1619 | 1938 | + | 0.31063 | |
g6433 | DLA_07159 | GAOABQK02JBK0O | CDS | 45121 | 2970 | - | 0.306734 | |
g6436 | DLA_07162 | GAOABQK02JBK0O | CDS | 55174 | 2730 | + | 0.323077 | |
g6467 | DLA_07196 | GAOABQK02JBK0O | CDS | 131417 | 2556 | + | 0.321205 | |
g6552 | DLA_07297 | GAOABQK02JOCCH | CDS | 107432 | 1428 | - | 0.338235 | |
g6599 | DLA_07351 | GAOABQK02JOCCH | CDS | 228160 | 1170 | - | 0.315385 | |
g6607 | DLA_07358 | GAOABQK02JOCCH | CDS | 240004 | 12681 | - | 0.328365 | |
g6614 | DLA_07365 | GAOABQK02JOCCH | CDS | 270577 | 426 | - | 0.284038 | |
g6686 | DLA_07446 | GAOABQK02JOCCH | CDS | 428514 | 2859 | - | 0.317943 | |
g6710 | DLA_07472 | GAOABQK02JOCCH | CDS | 467845 | 2673 | - | 0.329592 | |
g6711 | DLA_07474 | GAOABQK02JOCCH | CDS | 471109 | 7059 | - | 0.374982 | |
g6720 | DLA_07485 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GAOABQK02JOCCH | CDS | 494830 | 1011 | - | 0.318497 |
g6777 | DLA_07549 | GAOABQK02JOCCH | CDS | 627098 | 894 | - | 0.332215 | |
g6937 | DLA_04686 | GLQOFTK02FH5TG | CDS | 112858 | 411 | - | 0.29927 | |
g6969 | DLA_07767 | GLQOFTK02FH5TG | CDS | 179062 | 2796 | - | 0.363019 | |
g6985 | DLA_07786 | GLQOFTK02FH5TG | CDS | 212046 | 747 | + | 0.298527 | |
g73 | DLA_00084 | contig05409_1.exp | CDS | 173780 | 2514 | + | 0.356404 | |
g7346 | DLA_08210 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GLQOFTK02FH5TG | CDS | 1043861 | 1017 | + | 0.281219 |
g7430 | DLA_08309 | GLQOFTK02FH5TG | CDS | 1244453 | 2094 | - | 0.330946 | |
g7470 | DLA_08357 | GLQOFTK02FH5TG | CDS | 1338085 | 3267 | - | 0.329966 | |
g7475 | DLA_08365 | GLQOFTK02FH5TG | CDS | 1349218 | 11601 | - | 0.325403 | |
g7486 | DLA_08378 | GLQOFTK02FH5TG | CDS | 1383522 | 3045 | + | 0.314286 | |
g7539 | DLA_08433 | there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 1491296 | 2943 | + | 0.321441 |
g7566 | DLA_08462 | GLQOFTK02G2F2O | CDS | 8848 | 1590 | - | 0.31195 | |
g7576 | DLA_08474 | GLQOFTK02G2F2O | CDS | 31480 | 675 | - | 0.371852 | |
g7724 | DLA_08642 | GLQOFTK02G2F2O | CDS | 383694 | 4512 | - | 0.359043 | |
g7747 | DLA_08662 | conserved protein mainly among fungi and plants | GLQOFTK02G2F2O | CDS | 436087 | 2898 | + | 0.333333 |
g7934 | DLA_08869 | GLQOFTK02G2F2O | CDS | 837751 | 234 | + | 0.25641 | |
g7936 | DLA_08871 | GLQOFTK02G2F2O | CDS | 840428 | 2337 | + | 0.286264 | |
g8143 | DLA_09100 | GLQOFTK02G2F2O | CDS | 1346133 | 1419 | + | 0.384778 | |
g8197 | DLA_09154 | GLQOFTK02G2F2O | CDS | 1451518 | 3885 | - | 0.351351 | |
g8416 | DLA_09385 | GLQOFTK02G2F2O | CDS | 1890456 | 453 | + | 0.335541 | |
g8477 | DLA_09450 | SNARE protein interacts with AP180 (clmA) which retrieves Vamp7B from the contractile vacuole | GLQOFTK02G2F2O | CDS | 2028516 | 690 | + | 0.291304 |
g8508 | DLA_09484 | GLQOFTK02GHM7A | CDS | 38320 | 2019 | + | 0.301139 | |
g852 | DLA_00932 | F4PJNLW01A00V1 | CDS | 470736 | 10092 | + | 0.339279 | |
g8531 | DLA_09510 | GLQOFTK02GHM7A | CDS | 98002 | 2253 | + | 0.377275 | |
g8593 | DLA_09585 | GLQOFTK02GHM7A | CDS | 246755 | 4185 | + | 0.314934 | |
g8608 | DLA_09601 | GLQOFTK02GHM7A | CDS | 279919 | 3174 | - | 0.371456 | |
g891 | DLA_00983 | F4PJNLW01A00V1 | CDS | 569380 | 1380 | - | 0.301449 | |
g9041 | DLA_10062 | GLQOFTK02GQ36N | CDS | 387355 | 1842 | + | 0.290988 | |
g9098 | DLA_10129 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | GLQOFTK02GQ36N | CDS | 538065 | 4770 | - | 0.341719 |
g9158 | DLA_10199 | GLQOFTK02GUKFG | CDS | 11171 | 471 | - | 0.314225 | |
g9210 | DLA_10261 | GLQOFTK02GUKFG | CDS | 129499 | 4644 | + | 0.343239 | |
g9236 | DLA_10289 | GLQOFTK02GUKFG | CDS | 189555 | 1299 | + | 0.326405 | |
g9240 | DLA_10294 | GLQOFTK02GUKFG | CDS | 198640 | 1005 | + | 0.321393 | |
g9259 | DLA_10316 | GLQOFTK02GUKFG | CDS | 240693 | 10326 | + | 0.328879 | |
g9262 | DLA_10320 | GLQOFTK02GUKFG | CDS | 258563 | 918 | - | 0.262527 | |
g9270 | DLA_10328 | GLQOFTK02GUKFG | CDS | 292343 | 2208 | - | 0.347373 | |
g9339 | DLA_10412 | GLQOFTK02GUKFG | CDS | 436075 | 3642 | + | 0.354201 | |
g9445 | DLA_10523 | GLQOFTK02IIOHN | CDS | 85920 | 4386 | + | 0.332421 | |
g9499 | DLA_10589 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention in D. discoideum involved in early development and tip formation | GLQOFTK02IJPNF | CDS | 37254 | 10056 | - | 0.289081 |
g963 | DLA_01066 | F4PJNLW01A00V1 | CDS | 736130 | 7947 | - | 0.317227 | |
g9819 | DLA_10960 | GLQOFTK02JL55Q | CDS | 195158 | 1359 | + | 0.309051 | |
g9834 | DLA_10974 | GLQOFTK02JL55Q | CDS | 223375 | 3783 | + | 0.317209 | |
g9932 | DLA_11079 | GLQOFTK02JL55Q | CDS | 449060 | 2265 | + | 0.335099 | |
g9983 | DLA_11136 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GLQOFTK02JL55Q | CDS | 557966 | 924 | - | 0.311688 |
g9999 | DLA_11844 | belongs to the drugmetabolite transporter superfamily similar to human SLC35D1 (UDP-glucuronic acidUDP-N-acetylgalactosamine transporter) and S. cerevisiae VRG4 (GDP-mannose transporter 1) contains 8 putative transmembrane domains | GLQOFTK02JL55Q | CDS | 591072 | 942 | - | 0.321656 |
Polysphondylium pallidum, PN500 | ||||||||
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
g10019 | PPL_10545 | EXOLTKG01B86TH-3_part2 | CDS | 361931 | 4890 | - | 0.358896 | |
g1013 | PPL_01176 | DPPA0061d07.r1-5 | CDS | 895531 | 1098 | - | 0.367942 | |
g10163 | PPL_10694 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | EXOLTKG01B86TH-3_part2 | CDS | 810275 | 873 | - | 0.342497 |
g10187 | PPL_10723 | conserved protein mainly among fungi and plants | EXOLTKG01B86TH-3_part2 | CDS | 914488 | 2772 | - | 0.388889 |
g10247 | PPL_10793 | EXOLTKG01B86TH-3y_part1 | CDS | 163217 | 1197 | + | 0.35589 | |
g10303 | PPL_10857 | EXOLTKG01B86TH-3y_part1 | CDS | 346255 | 2988 | - | 0.380522 | |
g10437 | PPL_10993 | EXOLTKG02GJRTE-5 | CDS | 115626 | 1389 | + | 0.408927 | |
g10455 | PPL_11021 | EXOLTKG02GJRTE-5 | CDS | 186008 | 1197 | + | 0.380117 | |
g10532 | PPL_11114 | EXOLTKG02GJRTE-5 | CDS | 386252 | 1194 | + | 0.39196 | |
g10643 | PPL_11229 | PN500-F-W-a08d11.p658-5_part2 | CDS | 213021 | 7863 | + | 0.389419 | |
g10699 | PPL_11292 | PN500-F-W-a08d11.p658-5_part2 | CDS | 376552 | 2154 | - | 0.416435 | |
g10700 | PPL_11294 | involved in the unconventional secretory pathway of acbA the precurser of SDF-2 (spore differentiation factor 2) ortholog of the mammalian golgi reassembly stacking protein 2 (golgi reassembly-stacking protein of 55 kDa) | PN500-F-W-a08d11.p658-5_part2 | CDS | 380422 | 1053 | - | 0.362773 |
g1080 | PPL_01253 | DPPA0061d07.r1-5 | CDS | 1090897 | 438 | + | 0.312785 | |
g1089 | PPL_01263 | DPPA0061d07.r1-5 | CDS | 1117732 | 9486 | - | 0.364537 | |
g11007 | PPL_11754 | PN500-G-d-72b01.r1-5 | CDS | 40005 | 2631 | + | 0.405169 | |
g11047 | PPL_11799 | PN500-G-d-72b01.r1-5 | CDS | 173824 | 4362 | + | 0.392481 | |
g11214 | PPL_11968 | PN500-G-d-72b01.r1-5 | CDS | 631746 | 765 | + | 0.513726 | |
g11237 | PPL_11992 | PN500-G-d-72b01.r1-5 | CDS | 706934 | 390 | + | 0.366667 | |
g1145 | PPL_01333 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | DPPA0061d07.r1-5 | CDS | 1285022 | 4272 | - | 0.422285 |
g1220 | PPL_01427 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) | DPPA0090b03.f1-3_x_part2 | CDS | 92480 | 1521 | - | 0.450362 |
g1364 | PPL_01575 | DPPA0090b03.f1-3_x_part3 | CDS | 136946 | 2520 | + | 0.385714 | |
g1528 | PPL_01758 | DPPA0090b03.f1-3_x_part3 | CDS | 606734 | 3174 | - | 0.41966 | |
g1546 | PPL_01781 | putative ortholog of mammalian sorting nexin and S. cerevisiae VPS5 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | DPPA0090b03.f1-3_x_part3 | CDS | 663244 | 1596 | - | 0.452381 |
g1736 | PPL_01973 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention in D. discoideum involved in early development and tip formation | DPPA0090b03.f1-3_x_part3 | CDS | 1173296 | 10497 | + | 0.391445 |
g1847 | PPL_02097 | DPPA0090b03.f1-3_x_part3 | CDS | 1493464 | 4521 | - | 0.397921 | |
g1923 | PPL_02179 | DPPA0090b03.f1-3_x_part3 | CDS | 1756124 | 1422 | + | 0.459916 | |
g1960 | PPL_02219 | DPPA0090b03.f1-3_x_part3 | CDS | 1861223 | 405 | + | 0.34321 | |
g1973 | PPL_02232 | DPPA0090b03.f1-3_x_part3 | CDS | 1897024 | 645 | - | 0.420155 | |
g1985 | PPL_02243 | DPPA0090b03.f1-3_x_part3 | CDS | 1927047 | 3198 | - | 0.449343 | |
g2499 | PPL_02816 | DPPA0090b03.f1-3_y_part1 | CDS | 625558 | 210 | + | 0.37619 | |
g2513 | PPL_02832 | DPPA0090b03.f1-3_y_part1 | CDS | 665383 | 1809 | - | 0.389165 | |
g2537 | PPL_12961 | DPPA0090b03.f1-3_y_part1 | CDS | 720614 | 1902 | + | 0.384858 | |
g2569 | PPL_02889 | DPPA0090b03.f1-3_y_part1 | CDS | 792190 | 1977 | - | 0.418311 | |
g2597 | PPL_02927 | DPPA0090b03.f1-3_y_part1 | CDS | 867633 | 2898 | + | 0.352657 | |
g262 | PPL_00370 | DPPA0004F08.r1-5_part2 | CDS | 756907 | 1815 | + | 0.400551 | |
g2712 | PPL_03056 | DPPA0090b03.f1-3_y_part1 | CDS | 1208675 | 3255 | + | 0.369892 | |
g2840 | PPL_03195 | DPPA0090b03.f1-3_y_part1 | CDS | 1561591 | 2265 | + | 0.48521 | |
g2915 | PPL_13006 | DPPA0090b03.f1-3_y_part1 | CDS | 1761078 | 1470 | - | 0.395918 | |
g2916 | PPL_13007 | DPPA0090b03.f1-3_y_part1 | CDS | 1762796 | 990 | - | 0.352525 | |
g3100 | PPL_03479 | DPPA0090b03.f1-3_y_part1 | CDS | 2265988 | 1167 | + | 0.384747 | |
g336 | PPL_00448 | DPPA0004F08.r1-5_part2 | CDS | 966105 | 5640 | + | 0.382979 | |
g3363 | PPL_03809 | DPPB0337b12.r1-5 | CDS | 407514 | 1302 | + | 0.314132 | |
g3422 | PPL_13060 | DPPB0337b12.r1-5 | CDS | 556558 | 606 | - | 0.457096 | |
g354 | PPL_00469 | DPPA0004F08.r1-5_part2 | CDS | 1026696 | 1083 | - | 0.364728 | |
g3874 | PPL_04376 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | DPPB0360e11.f1-5 | CDS | 534091 | 11271 | + | 0.418242 |
g4036 | PPL_04555 | DPPB0360e11.f1-5 | CDS | 1024121 | 2805 | - | 0.357932 | |
g4037 | PPL_04557 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DPPB0360e11.f1-5 | CDS | 1027565 | 486 | + | 0.335391 |
g444 | PPL_00570 | DPPA0004F08.r1-5_part2 | CDS | 1291308 | 4569 | + | 0.408186 | |
g4451 | PPL_05043 | E0KFERV02EE9X2-3_part2 | CDS | 294882 | 4575 | + | 0.337486 | |
g4555 | PPL_05160 | E3JQK7F01CUWUC-3_part1 | CDS | 274732 | 2304 | + | 0.39974 | |
g4689 | PPL_05310 | E3JQK7F01EFZL8-5 | CDS | 152553 | 3174 | - | 0.431002 | |
g4717 | PPL_05342 | E3JQK7F01EFZL8-5 | CDS | 252782 | 663 | - | 0.333333 | |
g4751 | PPL_05382 | E3JQK7F01EFZL8-5 | CDS | 333513 | 3888 | + | 0.378344 | |
g483 | PPL_00616 | DPPA0004F08.r1-5_part2 | CDS | 1415720 | 1377 | - | 0.318809 | |
g5084 | PPL_05733 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | E3JQK7F01EFZL8-5 | CDS | 1255401 | 999 | - | 0.38038 |
g5283 | PPL_05936 | E3JQK7F02G10GF-5 | CDS | 369370 | 2643 | + | 0.430193 | |
g5324 | PPL_05973 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | E3JQK7F02G10GF-5 | CDS | 467402 | 1515 | - | 0.4 |
g5336 | PPL_05988 | E3JQK7F02G10GF-5 | CDS | 494787 | 13017 | + | 0.429515 | |
g5337 | PPL_05990 | E3JQK7F02G10GF-5 | CDS | 508064 | 2421 | + | 0.410574 | |
g5403 | PPL_06061 | E3JQK7F02G10GF-5 | CDS | 688975 | 2742 | + | 0.392779 | |
g547 | PPL_00680 | DPPA0004F08.r1-5_part3 | CDS | 42246 | 2229 | + | 0.41633 | |
g548 | PPL_00681 | DPPA0004F08.r1-5_part3 | CDS | 45400 | 5994 | + | 0.385385 | |
g6020 | PPL_06743 | E3JQK7F02HW0LE-5_part2 | CDS | 381256 | 999 | - | 0.337337 | |
g612 | PPL_00744 | DPPA0004F08.r1-5_part3 | CDS | 217250 | 3255 | + | 0.399693 | |
g6143 | PPL_06867 | E3JQK7F02HW0LE-5_part2 | CDS | 699716 | 585 | + | 0.355556 | |
g624 | PPL_00757 | DPPA0004F08.r1-5_part3 | CDS | 250439 | 2094 | + | 0.459408 | |
g6256 | PPL_06991 | E3JQK7F02HW0LE-5_part2 | CDS | 1011350 | 450 | + | 0.353333 | |
g6282 | PPL_07018 | E3JQK7F02HW0LE-5_part2 | CDS | 1092074 | 11724 | + | 0.408905 | |
g6507 | PPL_13337 | E3JQK7F02HW0LE-5_part2 | CDS | 1741142 | 309 | - | 0.423948 | |
g6556 | PPL_07329 | E3JQK7F02HW0LE-5_part2 | CDS | 1895638 | 4248 | + | 0.374294 | |
g6569 | PPL_07344 | E3JQK7F02HW0LE-5_part2 | CDS | 1934009 | 2601 | - | 0.332949 | |
g6577 | PPL_07352 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | E3JQK7F02HW0LE-5_part2 | CDS | 1955998 | 2202 | + | 0.391462 |
g6590 | PPL_07367 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | EVG8W8Q01C9YYY-5_part1 | CDS | 16396 | 906 | + | 0.343267 |
g6691 | PPL_07490 | EVG8W8Q01C9YYY-5_part2 | CDS | 101780 | 3150 | + | 0.439683 | |
g6714 | PPL_07515 | EVG8W8Q01C9YYY-5_part2 | CDS | 168200 | 12471 | + | 0.402614 | |
g6743 | PPL_07547 | EVG8W8Q01EEF2G-5 | CDS | 48390 | 1032 | - | 0.357558 | |
g6938 | PPL_07756 | EVG8W8Q02J3HU6-3_part1 | CDS | 265156 | 8928 | + | 0.429435 | |
g6939 | PPL_13363 | EVG8W8Q02J3HU6-3_part1 | CDS | 274408 | 672 | + | 0.470238 | |
g6971 | PPL_07795 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) there is a second copy of this gene | EVG8W8Q02J3HU6-3_part1 | CDS | 367438 | 1617 | - | 0.435374 |
g730 | PPL_00879 | DPPA0061d07.r1-5 | CDS | 86933 | 2058 | + | 0.498056 | |
g7397 | PPL_08255 | EVG8W8Q02J3HU6-3_part3 | CDS | 530148 | 1098 | + | 0.343352 | |
g7497 | PPL_08374 | EVG8W8Q02J3HU6-3_part3 | CDS | 798875 | 2067 | + | 0.396226 | |
g7653 | PPL_08555 | EVKQ3GG01CS5PZ-3_part1 | CDS | 25655 | 630 | + | 0.374603 | |
g7740 | PPL_08645 | EVKQ3GG01CS5PZ-3_part1 | CDS | 270006 | 5253 | + | 0.498572 | |
g7747 | PPL_08653 | EVKQ3GG01CS5PZ-3_part1 | CDS | 290822 | 3141 | + | 0.440942 | |
g7765 | PPL_08679 | EVKQ3GG01CS5PZ-3_part1 | CDS | 346735 | 2562 | - | 0.466432 | |
g7854 | PPL_08776 | EVKQ3GG01CS5PZ-3_part1 | CDS | 599212 | 2742 | + | 0.394602 | |
g7872 | PPL_08797 | EVKQ3GG01CS5PZ-3_part1 | CDS | 648048 | 2205 | - | 0.431746 | |
g788 | PPL_00949 | DPPA0061d07.r1-5 | CDS | 284858 | 759 | + | 0.382082 | |
g7925 | PPL_08856 | EVKQ3GG01CS5PZ-3_part1 | CDS | 834837 | 17361 | - | 0.415183 | |
g7975 | PPL_08913 | EVKQ3GG01CS5PZ-3_part1 | CDS | 986211 | 2535 | + | 0.347535 | |
g8005 | PPL_08948 | atypical protein kinase belongs to the PIKK family of protein kinases similar to transformationtranscription domain-associated protein (TRRAP) | EVKQ3GG01CS5PZ-3_part1 | CDS | 1078944 | 12966 | + | 0.429585 |
g8080 | PPL_09023 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | EVKQ3GG01CS5PZ-3_part1 | CDS | 1280112 | 5025 | + | 0.416119 |
g8342 | PPL_09302 | EVKQ3GG01CS5PZ-3_part2 | CDS | 153770 | 333 | - | 0.405405 | |
g8432 | PPL_09407 | EVKQ3GG01DB4K7-5 | CDS | 397 | 7002 | + | 0.458012 | |
g8520 | PPL_12138 | EVKQ3GG01DOIJB_part1 | CDS | 276503 | 1353 | + | 0.45898 | |
g8532 | PPL_12151 | EVKQ3GG01DOIJB_part1 | CDS | 307559 | 2151 | + | 0.41934 | |
g8540 | PPL_12160 | EVKQ3GG01DOIJB_part1 | CDS | 329340 | 3003 | - | 0.435231 | |
g8544 | PPL_12167 | EVKQ3GG01DOIJB_part1 | CDS | 351088 | 4431 | + | 0.425863 | |
g8548 | PPL_12172 | EVKQ3GG01DOIJB_part1 | CDS | 366638 | 1911 | + | 0.430665 | |
g8609 | PPL_12238 | EVKQ3GG01DOIJB_part1 | CDS | 527136 | 4446 | - | 0.421502 | |
g8701 | PPL_12338 | EVKQ3GG01DOIJB_part1 | CDS | 796585 | 3399 | - | 0.414828 | |
g9028 | PPL_09450 | EVKQ3GG02I325Y-5_part1 | CDS | 120492 | 1365 | + | 0.339194 | |
g9348 | PPL_09793 | EVKQ3GG02I325Y-5_part1 | CDS | 1025817 | 14310 | + | 0.361356 | |
g9355 | PPL_09797 | EVKQ3GG02I325Y-5_part1 | CDS | 1058152 | 13197 | + | 0.350004 | |
g9384 | PPL_09833 | EVKQ3GG02I325Y-5_part1 | CDS | 1164152 | 2010 | + | 0.390547 | |
g9429 | PPL_09886 | EVKQ3GG02I325Y-5_part1 | CDS | 1304371 | 2310 | - | 0.394805 | |
g9436 | PPL_09893 | EVKQ3GG02I325Y-5_part1 | CDS | 1323159 | 2460 | - | 0.408943 | |
g9516 | PPL_09989 | EWNM59D01C4IL7-5_part1 | CDS | 56570 | 651 | + | 0.344086 | |
g955 | PPL_01120 | homolog of H. sapiens TNPO12 and S. cervisiae KAP104 (karyopherin 104) involved in nuclear protein import | DPPA0061d07.r1-5 | CDS | 743453 | 2706 | - | 0.410569 |
g9593 | PPL_10069 | EWNM59D01C4IL7-5_part1 | CDS | 257541 | 2496 | - | 0.435497 | |
g9626 | PPL_10108 | EWNM59D01C4IL7-5_part1 | CDS | 354418 | 1527 | - | 0.391618 | |
g9757 | PPL_10258 | EWNM59D01C4IL7-5_part1 | CDS | 754110 | 3837 | - | 0.455304 | |
g9781 | PPL_10288 | EWNM59D01C4IL7-5_part1 | CDS | 826359 | 10395 | - | 0.389226 | |
g981 | PPL_12763 | DPPA0061d07.r1-5 | CDS | 809648 | 5637 | + | 0.361717 | |
g9824 | PPL_10340 | EWNM59D01C4IL7-5_part1 | CDS | 959812 | 3849 | + | 0.376202 | |
g9826 | PPL_10342 | EWNM59D01C4IL7-5_part1 | CDS | 964362 | 3678 | + | 0.383904 | |
g9994 | PPL_10523 | EXOLTKG01B86TH-3_part2 | CDS | 279739 | 2055 | + | 0.431144 |