© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|7431 |
| Gene name | |
| Location | Contig_431:239..4587 |
| Strand | - |
| Gene length (bp) | 4348 |
| Transcript length (bp) | 4182 |
| Coding sequence length (bp) | 4182 |
| Protein length (aa) | 1394 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF16212 | PhoLip_ATPase_C | Phospholipid-translocating P-type ATPase C-terminal | 5.9E-66 | 1071 | 1321 |
| PF16209 | PhoLip_ATPase_N | Phospholipid-translocating ATPase N-terminal | 4.1E-22 | 69 | 123 |
| PF00702 | Hydrolase | haloacid dehalogenase-like hydrolase | 8.2E-07 | 850 | 979 |
| PF13246 | Cation_ATPase | Cation transport ATPase (P-type) | 3.7E-10 | 604 | 697 |
| PF00122 | E1-E2_ATPase | E1-E2 ATPase | 2.0E-10 | 201 | 418 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 32 | 1370 | 0.0E+00 |
| sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 180 | 1321 | 0.0E+00 |
| sp|P39524|ATC3_YEAST | Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 | 23 | 698 | 4.0E-100 |
| sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 70 | 707 | 4.0E-98 |
| sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 56 | 702 | 4.0E-96 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 32 | 1370 | 0.0E+00 |
| sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 180 | 1321 | 0.0E+00 |
| sp|P39524|ATC3_YEAST | Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 | 23 | 698 | 4.0E-100 |
| sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 70 | 707 | 4.0E-98 |
| sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 56 | 702 | 4.0E-96 |
| sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 56 | 702 | 8.0E-96 |
| sp|O94296|YOOC_SCHPO | Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 | 70 | 698 | 5.0E-92 |
| sp|P57792|ALA12_ARATH | Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 | 70 | 707 | 4.0E-91 |
| sp|Q9LVK9|ALA7_ARATH | Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 | 70 | 698 | 1.0E-90 |
| sp|Q9SGG3|ALA5_ARATH | Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 | 60 | 698 | 1.0E-90 |
| sp|Q9SX33|ALA9_ARATH | Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 | 56 | 698 | 5.0E-90 |
| sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 832 | 1319 | 1.0E-89 |
| sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 832 | 1280 | 4.0E-89 |
| sp|Q9SLK6|ALA6_ARATH | Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 | 70 | 701 | 9.0E-89 |
| sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 832 | 1319 | 1.0E-88 |
| sp|Q9LI83|ALA10_ARATH | Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 | 70 | 698 | 2.0E-87 |
| sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 759 | 1273 | 1.0E-86 |
| sp|Q9LNQ4|ALA4_ARATH | Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 | 60 | 698 | 1.0E-86 |
| sp|Q9NTI2|AT8A2_HUMAN | Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 | 73 | 707 | 3.0E-86 |
| sp|P98200|AT8A2_MOUSE | Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 | 70 | 707 | 9.0E-86 |
| sp|Q9LNQ4|ALA4_ARATH | Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 | 833 | 1303 | 6.0E-83 |
| sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 818 | 1200 | 4.0E-82 |
| sp|Q9NTI2|AT8A2_HUMAN | Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 | 818 | 1200 | 6.0E-82 |
| sp|O94296|YOOC_SCHPO | Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 | 834 | 1306 | 1.0E-81 |
| sp|P39524|ATC3_YEAST | Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 | 823 | 1207 | 4.0E-81 |
| sp|P98204|ALA1_ARATH | Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 | 70 | 695 | 4.0E-81 |
| sp|P98200|AT8A2_MOUSE | Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 | 818 | 1200 | 5.0E-81 |
| sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 830 | 1240 | 2.0E-80 |
| sp|Q9Y2G3|AT11B_HUMAN | Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 | 70 | 697 | 4.0E-80 |
| sp|Q9SGG3|ALA5_ARATH | Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 | 833 | 1303 | 8.0E-80 |
| sp|Q9GKS6|AT10D_MACFA | Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 | 833 | 1176 | 1.0E-79 |
| sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 833 | 1275 | 2.0E-79 |
| sp|A3FIN4|AT8B5_MOUSE | Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 | 70 | 708 | 2.0E-79 |
| sp|P98198|AT8B2_HUMAN | Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 | 70 | 702 | 3.0E-79 |
| sp|P98199|AT8B2_MOUSE | Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 | 70 | 698 | 8.0E-79 |
| sp|Q9N0Z4|AT11B_RABIT | Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 | 70 | 697 | 2.0E-78 |
| sp|Q9LVK9|ALA7_ARATH | Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 | 833 | 1304 | 4.0E-78 |
| sp|Q9SLK6|ALA6_ARATH | Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 | 833 | 1304 | 2.0E-77 |
| sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 813 | 1256 | 2.0E-77 |
| sp|Q9LI83|ALA10_ARATH | Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 | 833 | 1304 | 1.0E-76 |
| sp|O60423|AT8B3_HUMAN | Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 | 70 | 698 | 8.0E-76 |
| sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 833 | 1304 | 1.0E-74 |
| sp|P98198|AT8B2_HUMAN | Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 | 826 | 1218 | 2.0E-74 |
| sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 834 | 1197 | 3.0E-74 |
| sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 833 | 1304 | 3.0E-74 |
| sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 824 | 1307 | 5.0E-74 |
| sp|P98199|AT8B2_MOUSE | Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 | 826 | 1218 | 6.0E-74 |
| sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 835 | 1313 | 7.0E-74 |
| sp|Q9SX33|ALA9_ARATH | Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 | 834 | 1307 | 8.0E-74 |
| sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 70 | 698 | 1.0E-73 |
| sp|P98196|AT11A_HUMAN | Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 | 70 | 698 | 1.0E-73 |
| sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 833 | 1307 | 1.0E-72 |
| sp|P32660|ATC5_YEAST | Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 | 70 | 719 | 2.0E-72 |
| sp|P32660|ATC5_YEAST | Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 | 834 | 1242 | 2.0E-72 |
| sp|Q12675|ATC4_YEAST | Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 | 834 | 1302 | 3.0E-72 |
| sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 813 | 1243 | 3.0E-72 |
| sp|P57792|ALA12_ARATH | Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 | 834 | 1307 | 5.0E-72 |
| sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 813 | 1236 | 8.0E-72 |
| sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 833 | 1313 | 1.0E-71 |
| sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 56 | 487 | 1.0E-70 |
| sp|Q9Y2G3|AT11B_HUMAN | Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 | 824 | 1307 | 1.0E-70 |
| sp|A3FIN4|AT8B5_MOUSE | Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 | 819 | 1200 | 2.0E-69 |
| sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 26 | 553 | 3.0E-69 |
| sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 835 | 1304 | 1.0E-68 |
| sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 70 | 487 | 2.0E-68 |
| sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 26 | 503 | 3.0E-68 |
| sp|P98196|AT11A_HUMAN | Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 | 839 | 1335 | 2.0E-67 |
| sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 833 | 1264 | 2.0E-67 |
| sp|P98204|ALA1_ARATH | Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 | 838 | 1185 | 6.0E-67 |
| sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 839 | 1346 | 1.0E-65 |
| sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 70 | 487 | 1.0E-65 |
| sp|Q9N0Z4|AT11B_RABIT | Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 | 824 | 1321 | 2.0E-65 |
| sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 212 | 698 | 3.0E-64 |
| sp|Q12675|ATC4_YEAST | Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 | 69 | 698 | 5.0E-64 |
| sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 66 | 494 | 5.0E-64 |
| sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 834 | 1307 | 1.0E-63 |
| sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 70 | 487 | 5.0E-63 |
| sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 70 | 503 | 6.0E-63 |
| sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 73 | 487 | 9.0E-63 |
| sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 42 | 483 | 1.0E-62 |
| sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 70 | 501 | 2.0E-62 |
| sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 65 | 494 | 2.0E-62 |
| sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 834 | 1307 | 3.0E-62 |
| sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 70 | 504 | 1.0E-61 |
| sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 66 | 487 | 2.0E-61 |
| sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 174 | 699 | 9.0E-61 |
| sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 66 | 506 | 4.0E-58 |
| sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 64 | 484 | 1.0E-56 |
| sp|O60423|AT8B3_HUMAN | Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 | 838 | 1280 | 2.0E-56 |
| sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 64 | 484 | 4.0E-55 |
| sp|F1Q4S1|ATP9B_DANRE | Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 | 837 | 1274 | 4.0E-54 |
| sp|O43861|ATP9B_HUMAN | Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 | 837 | 1272 | 5.0E-53 |
| sp|P98195|ATP9B_MOUSE | Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 | 837 | 1272 | 1.0E-52 |
| sp|O70228|ATP9A_MOUSE | Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 | 837 | 1203 | 2.0E-52 |
| sp|D4ABB8|ATP9B_RAT | Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 | 837 | 1272 | 2.0E-52 |
| sp|O75110|ATP9A_HUMAN | Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 | 837 | 1203 | 2.0E-52 |
| sp|D4ABB8|ATP9B_RAT | Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 | 73 | 743 | 4.0E-52 |
| sp|P98195|ATP9B_MOUSE | Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 | 73 | 743 | 5.0E-52 |
| sp|A1A4J6|ATP9B_BOVIN | Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 | 837 | 1203 | 7.0E-52 |
| sp|F1Q4S1|ATP9B_DANRE | Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 | 70 | 748 | 1.0E-51 |
| sp|P40527|ATC7_YEAST | Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 | 45 | 694 | 1.0E-50 |
| sp|O43861|ATP9B_HUMAN | Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 | 73 | 737 | 3.0E-50 |
| sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 73 | 490 | 2.0E-49 |
| sp|A1A4J6|ATP9B_BOVIN | Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 | 73 | 737 | 4.0E-49 |
| sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 988 | 1198 | 2.0E-48 |
| sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 837 | 1321 | 2.0E-48 |
| sp|P40527|ATC7_YEAST | Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 | 837 | 1274 | 6.0E-47 |
| sp|O70228|ATP9A_MOUSE | Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 | 65 | 793 | 1.0E-46 |
| sp|O75110|ATP9A_HUMAN | Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 | 65 | 793 | 2.0E-46 |
| sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 997 | 1257 | 2.0E-42 |
| sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 70 | 516 | 5.0E-36 |
| sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 22 | 152 | 1.0E-24 |
| sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 835 | 940 | 2.0E-22 |
| sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 838 | 940 | 1.0E-21 |
| sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 577 | 698 | 2.0E-20 |
| sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 574 | 698 | 2.0E-20 |
| sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 590 | 702 | 5.0E-20 |
| sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 595 | 698 | 9.0E-20 |
| sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 595 | 698 | 3.0E-19 |
| sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 575 | 698 | 5.0E-19 |
| sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 575 | 698 | 1.0E-18 |
| sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 586 | 699 | 1.0E-18 |
| sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 574 | 699 | 3.0E-16 |
| sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 587 | 698 | 3.0E-15 |
| sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 588 | 694 | 1.0E-14 |
| sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 580 | 721 | 3.0E-13 |
| sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 594 | 721 | 3.0E-12 |
| sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 595 | 696 | 6.0E-12 |
| sp|Q3TYU2|AT135_MOUSE | Probable cation-transporting ATPase 13A5 OS=Mus musculus GN=Atp13a5 PE=2 SV=2 | 822 | 1067 | 3.0E-11 |
| sp|Q5ZKB7|AT134_CHICK | Probable cation-transporting ATPase 13A4 OS=Gallus gallus GN=ATP13A4 PE=2 SV=1 | 868 | 1067 | 4.0E-10 |
| sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 612 | 699 | 2.0E-09 |
| sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 604 | 698 | 2.0E-09 |
| sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 72 | 156 | 3.0E-09 |
| sp|Q4VNC1|AT134_HUMAN | Probable cation-transporting ATPase 13A4 OS=Homo sapiens GN=ATP13A4 PE=2 SV=3 | 852 | 1067 | 3.0E-09 |
| sp|Q9H7F0|AT133_HUMAN | Probable cation-transporting ATPase 13A3 OS=Homo sapiens GN=ATP13A3 PE=1 SV=4 | 835 | 1071 | 8.0E-09 |
| sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 549 | 702 | 2.0E-08 |
| sp|Q21286|YBF7_CAEEL | Probable cation-transporting ATPase K07E3.7 OS=Caenorhabditis elegans GN=K07E3.7/K07E3.6 PE=3 SV=4 | 835 | 1071 | 2.0E-08 |
| sp|Q5XF89|AT133_MOUSE | Probable cation-transporting ATPase 13A3 OS=Mus musculus GN=Atp13a3 PE=1 SV=1 | 833 | 1071 | 2.0E-08 |
| sp|Q5XF90|AT134_MOUSE | Probable cation-transporting ATPase 13A4 OS=Mus musculus GN=Atp13a4 PE=2 SV=1 | 884 | 1067 | 4.0E-08 |
| sp|Q9GKS6|AT10D_MACFA | Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 | 612 | 702 | 9.0E-08 |
| sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 603 | 751 | 1.0E-07 |
| sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 604 | 699 | 1.0E-07 |
| sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 73 | 148 | 1.0E-07 |
| sp|Q9WV27|AT1A4_MOUSE | Sodium/potassium-transporting ATPase subunit alpha-4 OS=Mus musculus GN=Atp1a4 PE=1 SV=3 | 888 | 1066 | 4.0E-07 |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 45 | 0.45 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 356 | 378 | 22 |
| 2 | 399 | 421 | 22 |
| 3 | 1136 | 1155 | 19 |
| 4 | 1185 | 1204 | 19 |
| 5 | 1219 | 1241 | 22 |
| 6 | 1248 | 1265 | 17 |
| 7 | 1295 | 1317 | 22 |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
| Protein | >Hirsu2|7431 MSTTQSTTTEKHSVYDSVHLAPSPTPFNHATIADFVLCRKRSQASKHGRCIPLAIERQTPLIDARRGCAYISNNV RTSRYTIWDFVPKQLFFQFSRIGNFYFLCVAIPQTIPGLSTTGNFTTMLPLCFFVLVTMAKEGYDDYRRHRLDKI ENANLATVLGRESKYADGAESHGPLSRWNPFRTKTTGRPRSAPADDIQGVGWVPVRWSHVKVGDIVLLSRDEPVP ADLVLLHSDDEDGVAYIDTMALDGETNLKSKQVCHALEGCNSIKGIASCPAQFAVEDPNPNLFDFKGRVAVGDKA APLTPNHVIYRGSVMRNTTCAMGLVINTGEECKVRMNANQHPTAKRPALEKIVNRVVIILAIYVMVLSVGIATGY LKWQSDFERKAWYLDRAAVPFHQILIAFVIMFNNIVPLSLYITLEIIKVGQLLLVNSDVNMYHEETDTPARCNTN TILENLGQVGYIFSDKTGTLTDNIMKFRKLSVAGTVWLHEMDLQPSEPDQNPVPTPRDGLPSLRPLPDKAGPSTL VIPEDYSDAAETPTSPARSSLGHRPSSHWRSTGRPDHVQPEVNTSDLLDYMRSRPHSAFSRKARECMISVAICHT CLPEHKDGSIEYQASSPDELALVKASQELGYQVTNRTSQSMTLQVPRPNGQVDKMVFQILDVIEFSSTRKRMSII VRYPDGRISLICKGADSAILPRLKLSSLAMQKAGEVRKSADLEREMHRRSEQQEPRNSFGGRPSLTVHRNHGVMR DASLSRRPVASRSKSFEINKLARSSVDRVRVSLSSPRGASLDVSRAQFANPPALHSRSAHDRMDFLDDPSIFDES EVFTRCFKHIDDFATEGLRTLIYAQKFISEQEYIEWKGLYDEATTSLDNRQEMIEAAGEKIEQSFDLVGATAIED KLQRGVPETIDKLRRANIRIWMLTGDKRETAINIAHSARICRPASDLFVLDATKGSLWSQLAALAEDLQEGSVHS VMVVDGQTLAAVEKSAELSQRFFDLAVLVDSVICCRAAPAQKALLVRAVRSRLCAAKGKHRHGLTLAIGDGANDI AMIQESHVGIGISGQEGLQAARIADYSIAQFRFLQRMLLVHGRWNYIRTAKFILCTFWKELFFYLPAAQFQRLNG YSGTSLFQETSLTVFNTLFTSLCTICMGIWEQDLRAETLLAVPELYVYGQRDLGLNMSKYLRWMFLACVEGVIVF HGAWAGYGLIEPGIRDSGLYPLGTLVFTLAVFWINWKLLIFETHYKTAIVIGSFFLTTVGWWAWLSFLDEVFPLM PSGPNAVHDSFTKHWGQDAAWWATVFLVLTVLGAIGACGKVVKRQMLLAGFWQWPPWRRRRRLSDNVEEWDLELW QELEQDPVVREQLRALARDEGSPADEAAAAEDGAEPGTATAKA* |
| Coding | >Hirsu2|7431 ATGTCCACGACTCAATCCACCACCACCGAGAAACACTCCGTCTACGATTCCGTCCACTTGGCCCCCAGTCCGACT CCCTTCAACCACGCCACCATCGCCGACTTCGTTCTGTGCCGAAAGCGCTCCCAGGCCTCCAAGCATGGGCGATGC ATTCCCCTCGCCATTGAGCGCCAGACGCCCTTAATCGACGCCCGACGTGGTTGCGCATACATCTCCAACAATGTC CGGACTTCTCGCTATACCATCTGGGACTTTGTCCCAAAACAGCTTTTTTTTCAGTTCTCCCGCATCGGAAACTTC TATTTCCTCTGCGTCGCCATTCCCCAGACCATACCGGGCCTGTCCACCACTGGTAACTTTACCACAATGTTGCCC CTCTGCTTCTTCGTCCTTGTTACCATGGCGAAGGAGGGCTACGATGACTACAGGAGACATCGCTTGGACAAGATC GAGAATGCCAATCTCGCCACTGTTCTCGGCCGCGAGAGCAAGTACGCCGACGGAGCCGAGTCACACGGTCCCCTG AGCCGCTGGAATCCCTTTCGCACCAAGACAACTGGCCGGCCCAGATCAGCCCCGGCTGATGACATCCAGGGCGTC GGCTGGGTGCCGGTCAGATGGAGCCATGTTAAGGTCGGCGATATCGTCCTGCTATCCCGCGATGAGCCGGTTCCT GCCGACCTGGTTCTGCTCCACAGCGATGACGAGGATGGCGTCGCATACATCGACACCATGGCACTGGACGGCGAG ACGAACCTCAAGTCCAAGCAGGTCTGCCACGCTCTCGAGGGTTGCAATTCGATCAAGGGCATAGCATCTTGCCCC GCCCAATTCGCCGTCGAAGATCCAAACCCCAATCTATTTGACTTCAAGGGCCGTGTCGCCGTCGGCGACAAGGCG GCGCCGCTCACTCCCAACCACGTCATCTATCGCGGGAGCGTGATGCGCAACACCACCTGCGCCATGGGTCTGGTC ATCAACACGGGCGAAGAGTGCAAGGTCAGAATGAATGCGAATCAGCACCCCACCGCGAAACGCCCAGCTCTCGAG AAGATTGTCAACAGAGTCGTCATCATCCTGGCCATCTACGTGATGGTCCTGTCAGTCGGCATCGCCACGGGCTAC TTAAAGTGGCAGAGCGACTTCGAACGAAAGGCTTGGTATCTCGATCGCGCCGCTGTTCCCTTCCACCAGATCCTC ATTGCATTTGTCATCATGTTCAACAACATCGTACCCTTGTCCCTGTACATCACCTTAGAGATCATCAAGGTCGGA CAGCTCTTACTTGTCAACTCGGACGTGAACATGTATCACGAGGAGACGGACACTCCGGCACGATGCAACACAAAT ACCATTTTGGAGAACCTGGGGCAGGTTGGCTACATCTTCTCCGACAAGACCGGAACTTTGACGGACAACATCATG AAGTTCCGCAAGCTCAGTGTCGCCGGCACCGTTTGGCTGCACGAGATGGACCTCCAGCCGTCCGAGCCGGATCAG AACCCCGTCCCGACGCCCCGCGACGGGCTCCCCTCGCTGAGGCCGCTTCCCGATAAGGCCGGGCCCAGCACCTTG GTCATCCCGGAGGATTATAGCGACGCGGCCGAAACGCCCACGTCACCCGCCAGGTCGTCCTTGGGCCACAGGCCA TCGTCCCACTGGCGGTCGACTGGTCGTCCCGACCATGTCCAACCCGAAGTCAACACGTCGGATCTCCTGGATTAC ATGCGATCCCGTCCGCACTCGGCTTTCTCTAGGAAGGCGAGAGAGTGCATGATTTCTGTCGCCATCTGCCATACC TGTCTGCCCGAACACAAGGACGGCAGTATCGAGTACCAGGCATCGTCACCCGATGAGCTGGCCCTAGTGAAGGCG TCACAGGAACTCGGCTACCAGGTGACGAACCGCACGTCGCAATCCATGACCCTGCAGGTCCCGCGGCCGAATGGC CAGGTCGATAAGATGGTCTTCCAGATCTTGGATGTGATTGAGTTCAGCAGTACGCGCAAGAGAATGTCCATCATC GTCCGCTATCCCGACGGGCGCATCTCCCTCATTTGCAAGGGCGCCGATTCGGCTATCCTGCCACGACTGAAACTT TCCTCGCTGGCCATGCAAAAGGCAGGCGAGGTCCGCAAGAGTGCCGATCTCGAGCGCGAGATGCATCGCCGTAGT GAGCAGCAGGAGCCCCGGAATAGCTTTGGCGGGAGGCCGAGCCTGACCGTCCATCGCAACCACGGAGTTATGAGG GACGCGAGCTTGAGTCGGCGGCCGGTCGCCAGCAGAAGCAAGTCGTTCGAGATTAACAAGCTCGCCCGATCGTCC GTCGACCGAGTTCGAGTCTCGCTCTCCTCCCCGCGCGGCGCCTCACTCGATGTGTCGCGCGCTCAGTTTGCGAAT CCGCCAGCTCTCCACTCGCGGTCCGCGCATGATCGCATGGATTTCCTGGACGACCCCTCCATCTTCGACGAGTCG GAAGTCTTCACAAGGTGTTTCAAGCACATCGACGACTTTGCAACAGAGGGCCTCCGGACGCTGATCTACGCTCAA AAGTTCATCTCGGAGCAGGAGTATATTGAGTGGAAAGGGCTCTACGACGAAGCGACGACGAGCCTCGACAACCGG CAGGAGATGATTGAAGCCGCCGGAGAAAAGATTGAGCAGTCGTTCGACCTCGTCGGTGCCACCGCTATCGAGGAC AAACTTCAGCGTGGCGTGCCCGAGACTATCGACAAGCTGCGACGTGCCAACATCAGGATATGGATGCTCACTGGC GACAAGCGCGAAACGGCCATCAACATTGCTCATTCGGCGCGCATATGCCGGCCCGCTTCGGATCTGTTCGTCCTG GACGCGACCAAGGGCTCTCTATGGTCGCAGCTCGCTGCCTTGGCCGAAGACCTGCAAGAGGGTTCCGTCCACAGC GTCATGGTCGTCGACGGGCAGACTCTGGCAGCCGTGGAGAAGTCGGCCGAGCTATCACAGAGGTTTTTTGACCTC GCCGTTCTCGTCGACTCCGTCATATGCTGCCGGGCCGCGCCGGCCCAGAAGGCGTTATTGGTGCGGGCTGTGCGC TCTCGCCTGTGTGCTGCCAAGGGAAAGCATCGCCACGGGTTGACGCTGGCCATTGGCGATGGCGCAAACGACATC GCCATGATCCAAGAAAGTCACGTTGGCATAGGAATCTCGGGACAGGAGGGCCTGCAGGCGGCGCGCATCGCCGAC TACTCCATAGCGCAGTTCCGGTTTCTGCAGAGGATGCTCCTCGTCCACGGGCGCTGGAACTACATCCGGACCGCA AAGTTCATCCTCTGCACCTTCTGGAAAGAGCTGTTTTTCTATCTCCCGGCCGCACAGTTCCAAAGACTTAATGGT TACAGCGGCACCTCGCTGTTCCAGGAGACGAGCCTGACCGTCTTCAACACGCTCTTCACCAGTCTCTGCACCATC TGTATGGGCATCTGGGAGCAGGACCTGAGAGCCGAAACGCTGCTCGCCGTGCCGGAGCTCTACGTGTACGGGCAG CGCGACCTGGGGCTGAACATGAGCAAATATCTGCGCTGGATGTTCCTGGCATGCGTGGAAGGCGTCATTGTCTTT CACGGCGCCTGGGCAGGCTACGGATTGATCGAGCCGGGCATCCGCGACTCGGGTCTGTACCCCCTGGGGACGCTC GTCTTCACGTTGGCGGTCTTCTGGATCAACTGGAAGCTACTCATTTTCGAGACGCACTACAAGACGGCCATCGTC ATCGGCTCCTTCTTCCTCACGACCGTGGGCTGGTGGGCCTGGCTCTCCTTCCTCGACGAAGTCTTCCCGCTGATG CCTTCGGGGCCCAACGCCGTCCACGACTCGTTCACCAAGCACTGGGGCCAGGACGCAGCCTGGTGGGCGACGGTC TTCCTCGTCCTCACCGTCCTCGGCGCGATCGGGGCCTGTGGCAAGGTGGTCAAGCGGCAGATGCTCCTGGCCGGC TTCTGGCAGTGGCCGCCGTGGCGGAGACGGCGGAGGCTGAGCGACAATGTGGAGGAGTGGGACCTGGAGCTGTGG CAGGAGCTGGAGCAGGACCCGGTCGTGCGCGAGCAGCTGAGGGCCCTGGCCCGGGACGAGGGCTCGCCGGCCGAC GAGGCGGCGGCCGCGGAGGACGGGGCCGAGCCCGGGACGGCCACGGCCAAGGCCTGA |
| Transcript | >Hirsu2|7431 ATGTCCACGACTCAATCCACCACCACCGAGAAACACTCCGTCTACGATTCCGTCCACTTGGCCCCCAGTCCGACT CCCTTCAACCACGCCACCATCGCCGACTTCGTTCTGTGCCGAAAGCGCTCCCAGGCCTCCAAGCATGGGCGATGC ATTCCCCTCGCCATTGAGCGCCAGACGCCCTTAATCGACGCCCGACGTGGTTGCGCATACATCTCCAACAATGTC CGGACTTCTCGCTATACCATCTGGGACTTTGTCCCAAAACAGCTTTTTTTTCAGTTCTCCCGCATCGGAAACTTC TATTTCCTCTGCGTCGCCATTCCCCAGACCATACCGGGCCTGTCCACCACTGGTAACTTTACCACAATGTTGCCC CTCTGCTTCTTCGTCCTTGTTACCATGGCGAAGGAGGGCTACGATGACTACAGGAGACATCGCTTGGACAAGATC GAGAATGCCAATCTCGCCACTGTTCTCGGCCGCGAGAGCAAGTACGCCGACGGAGCCGAGTCACACGGTCCCCTG AGCCGCTGGAATCCCTTTCGCACCAAGACAACTGGCCGGCCCAGATCAGCCCCGGCTGATGACATCCAGGGCGTC GGCTGGGTGCCGGTCAGATGGAGCCATGTTAAGGTCGGCGATATCGTCCTGCTATCCCGCGATGAGCCGGTTCCT GCCGACCTGGTTCTGCTCCACAGCGATGACGAGGATGGCGTCGCATACATCGACACCATGGCACTGGACGGCGAG ACGAACCTCAAGTCCAAGCAGGTCTGCCACGCTCTCGAGGGTTGCAATTCGATCAAGGGCATAGCATCTTGCCCC GCCCAATTCGCCGTCGAAGATCCAAACCCCAATCTATTTGACTTCAAGGGCCGTGTCGCCGTCGGCGACAAGGCG GCGCCGCTCACTCCCAACCACGTCATCTATCGCGGGAGCGTGATGCGCAACACCACCTGCGCCATGGGTCTGGTC ATCAACACGGGCGAAGAGTGCAAGGTCAGAATGAATGCGAATCAGCACCCCACCGCGAAACGCCCAGCTCTCGAG AAGATTGTCAACAGAGTCGTCATCATCCTGGCCATCTACGTGATGGTCCTGTCAGTCGGCATCGCCACGGGCTAC TTAAAGTGGCAGAGCGACTTCGAACGAAAGGCTTGGTATCTCGATCGCGCCGCTGTTCCCTTCCACCAGATCCTC ATTGCATTTGTCATCATGTTCAACAACATCGTACCCTTGTCCCTGTACATCACCTTAGAGATCATCAAGGTCGGA CAGCTCTTACTTGTCAACTCGGACGTGAACATGTATCACGAGGAGACGGACACTCCGGCACGATGCAACACAAAT ACCATTTTGGAGAACCTGGGGCAGGTTGGCTACATCTTCTCCGACAAGACCGGAACTTTGACGGACAACATCATG AAGTTCCGCAAGCTCAGTGTCGCCGGCACCGTTTGGCTGCACGAGATGGACCTCCAGCCGTCCGAGCCGGATCAG AACCCCGTCCCGACGCCCCGCGACGGGCTCCCCTCGCTGAGGCCGCTTCCCGATAAGGCCGGGCCCAGCACCTTG GTCATCCCGGAGGATTATAGCGACGCGGCCGAAACGCCCACGTCACCCGCCAGGTCGTCCTTGGGCCACAGGCCA TCGTCCCACTGGCGGTCGACTGGTCGTCCCGACCATGTCCAACCCGAAGTCAACACGTCGGATCTCCTGGATTAC ATGCGATCCCGTCCGCACTCGGCTTTCTCTAGGAAGGCGAGAGAGTGCATGATTTCTGTCGCCATCTGCCATACC TGTCTGCCCGAACACAAGGACGGCAGTATCGAGTACCAGGCATCGTCACCCGATGAGCTGGCCCTAGTGAAGGCG TCACAGGAACTCGGCTACCAGGTGACGAACCGCACGTCGCAATCCATGACCCTGCAGGTCCCGCGGCCGAATGGC CAGGTCGATAAGATGGTCTTCCAGATCTTGGATGTGATTGAGTTCAGCAGTACGCGCAAGAGAATGTCCATCATC GTCCGCTATCCCGACGGGCGCATCTCCCTCATTTGCAAGGGCGCCGATTCGGCTATCCTGCCACGACTGAAACTT TCCTCGCTGGCCATGCAAAAGGCAGGCGAGGTCCGCAAGAGTGCCGATCTCGAGCGCGAGATGCATCGCCGTAGT GAGCAGCAGGAGCCCCGGAATAGCTTTGGCGGGAGGCCGAGCCTGACCGTCCATCGCAACCACGGAGTTATGAGG GACGCGAGCTTGAGTCGGCGGCCGGTCGCCAGCAGAAGCAAGTCGTTCGAGATTAACAAGCTCGCCCGATCGTCC GTCGACCGAGTTCGAGTCTCGCTCTCCTCCCCGCGCGGCGCCTCACTCGATGTGTCGCGCGCTCAGTTTGCGAAT CCGCCAGCTCTCCACTCGCGGTCCGCGCATGATCGCATGGATTTCCTGGACGACCCCTCCATCTTCGACGAGTCG GAAGTCTTCACAAGGTGTTTCAAGCACATCGACGACTTTGCAACAGAGGGCCTCCGGACGCTGATCTACGCTCAA AAGTTCATCTCGGAGCAGGAGTATATTGAGTGGAAAGGGCTCTACGACGAAGCGACGACGAGCCTCGACAACCGG CAGGAGATGATTGAAGCCGCCGGAGAAAAGATTGAGCAGTCGTTCGACCTCGTCGGTGCCACCGCTATCGAGGAC AAACTTCAGCGTGGCGTGCCCGAGACTATCGACAAGCTGCGACGTGCCAACATCAGGATATGGATGCTCACTGGC GACAAGCGCGAAACGGCCATCAACATTGCTCATTCGGCGCGCATATGCCGGCCCGCTTCGGATCTGTTCGTCCTG GACGCGACCAAGGGCTCTCTATGGTCGCAGCTCGCTGCCTTGGCCGAAGACCTGCAAGAGGGTTCCGTCCACAGC GTCATGGTCGTCGACGGGCAGACTCTGGCAGCCGTGGAGAAGTCGGCCGAGCTATCACAGAGGTTTTTTGACCTC GCCGTTCTCGTCGACTCCGTCATATGCTGCCGGGCCGCGCCGGCCCAGAAGGCGTTATTGGTGCGGGCTGTGCGC TCTCGCCTGTGTGCTGCCAAGGGAAAGCATCGCCACGGGTTGACGCTGGCCATTGGCGATGGCGCAAACGACATC GCCATGATCCAAGAAAGTCACGTTGGCATAGGAATCTCGGGACAGGAGGGCCTGCAGGCGGCGCGCATCGCCGAC TACTCCATAGCGCAGTTCCGGTTTCTGCAGAGGATGCTCCTCGTCCACGGGCGCTGGAACTACATCCGGACCGCA AAGTTCATCCTCTGCACCTTCTGGAAAGAGCTGTTTTTCTATCTCCCGGCCGCACAGTTCCAAAGACTTAATGGT TACAGCGGCACCTCGCTGTTCCAGGAGACGAGCCTGACCGTCTTCAACACGCTCTTCACCAGTCTCTGCACCATC TGTATGGGCATCTGGGAGCAGGACCTGAGAGCCGAAACGCTGCTCGCCGTGCCGGAGCTCTACGTGTACGGGCAG CGCGACCTGGGGCTGAACATGAGCAAATATCTGCGCTGGATGTTCCTGGCATGCGTGGAAGGCGTCATTGTCTTT CACGGCGCCTGGGCAGGCTACGGATTGATCGAGCCGGGCATCCGCGACTCGGGTCTGTACCCCCTGGGGACGCTC GTCTTCACGTTGGCGGTCTTCTGGATCAACTGGAAGCTACTCATTTTCGAGACGCACTACAAGACGGCCATCGTC ATCGGCTCCTTCTTCCTCACGACCGTGGGCTGGTGGGCCTGGCTCTCCTTCCTCGACGAAGTCTTCCCGCTGATG CCTTCGGGGCCCAACGCCGTCCACGACTCGTTCACCAAGCACTGGGGCCAGGACGCAGCCTGGTGGGCGACGGTC TTCCTCGTCCTCACCGTCCTCGGCGCGATCGGGGCCTGTGGCAAGGTGGTCAAGCGGCAGATGCTCCTGGCCGGC TTCTGGCAGTGGCCGCCGTGGCGGAGACGGCGGAGGCTGAGCGACAATGTGGAGGAGTGGGACCTGGAGCTGTGG CAGGAGCTGGAGCAGGACCCGGTCGTGCGCGAGCAGCTGAGGGCCCTGGCCCGGGACGAGGGCTCGCCGGCCGAC GAGGCGGCGGCCGCGGAGGACGGGGCCGAGCCCGGGACGGCCACGGCCAAGGCCTGA |
| Gene | >Hirsu2|7431 ATGTCCACGACTCAATCCACCACCACCGAGAAACACTCCGTCTACGATTCCGTCCACTTGGCCCCCAGTCCGACT CCCTTCAACCACGGTGCTTCCTCAAGGCCGTCTCTGCGGGCCCGTCTTCGACGCTCGCTCGGCGCTGTCTCTCCA GCCACCATCGCCGACTTCGTTCTGTGCCGAAAGCGCTCCCAGGCCTCCAAGCATGGGCGATGCATTCCCCTCGCC ATTGAGCGCCAGACGCCCTTAATCGACGCCCGACGTGGTTGCGCATACATCTCCAACAATGTCCGGACTTCTCGC TATACCATCTGGGACTTTGTCCCAAAACAGCTTTTTTTTCAGTTCTCCCGCATCGGAAACTTCTATTTCCTCTGC GTCGCCATTCCCCAGACCGTATGTGTCCCTTGACTGCTTCTCGGGGCCGCTGCTGACTGCCGACCAAGATACCGG GCCTGTCCACCACTGGTAACTTTACCACAATGTTGCCCCTCTGCTTCTTCGTCCTTGTTACCATGGCGAAGGAGG GCTACGATGACTACAGGAGACATCGCTTGGACAAGATCGAGAATGCCAATCTCGCCACTGTTCTCGGCCGCGAGA GCAAGTACGCCGACGGAGCCGAGTCACACGGTCCCCTGAGCCGCTGGAATCCCTTTCGCACCAAGACAACTGGCC GGCCCAGATCAGCCCCGGCTGATGACATCCAGGGCGTCGGCTGGGTGCCGGTCAGATGGAGCCATGTTAAGGTCG GCGATATCGTCCTGCTATCCCGCGATGAGCCGGTTCCTGCCGACCTGGTTCTGCTCCACAGCGATGACGAGGATG GCGTCGCATACATCGACACCATGGCACTGGACGGCGAGACGAACCTCAAGTCCAAGCAGGTCTGCCACGCTCTCG AGGGTTGCAATTCGATCAAGGGCATAGCATCTTGCCCCGCCCAATTCGCCGTCGAAGATCCAAACCCCAATCTAT TTGACTTCAAGGGCCGTGTCGCCGTCGGCGACAAGGCGGCGCCGCTCACTCCCAACCACGTCATCTATCGCGGGA GCGTGATGCGCAACACCACCTGCGCCATGGGTCTGGTCATCAACACGGGCGAAGAGTGCAAGGTCAGAATGAATG CGAATCAGCACCCCACCGCGAAACGCCCAGCTCTCGAGAAGATTGTCAACAGAGTCGTCATCATCCTGGCCATCT ACGTGATGGTCCTGTCAGTCGGCATCGCCACGGGCTACTTAAAGTGGCAGAGCGACTTCGAACGAAAGGCTTGGT ATCTCGATCGCGCCGCTGTTCCCTTCCACCAGATCCTCATTGCATTTGTCATCATGTTCAACAACATCGTACCCT TGTCCCTGTACATCACCTTAGAGATCATCAAGGTCGGACAGCTCTTACTTGTCAACTCGGACGTGAACATGTATC ACGAGGAGACGGACACTCCGGCACGATGCAACACAAATACCATTTTGGAGAACCTGGGGCAGGTTGGCTACATCT TCTCCGACAAGACCGGAACTTTGACGGACAACATCATGAAGTTCCGCAAGCTCAGTGTCGCCGGCACCGTTTGGC TGCACGAGATGGACCTCCAGCCGTCCGAGCCGGATCAGAACCCCGTCCCGACGCCCCGCGACGGGCTCCCCTCGC TGAGGCCGCTTCCCGATAAGGCCGGGCCCAGCACCTTGGTCATCCCGGAGGATTATAGCGACGCGGCCGAAACGC CCACGTCACCCGCCAGGTCGTCCTTGGGCCACAGGCCATCGTCCCACTGGCGGTCGACTGGTCGTCCCGACCATG TCCAACCCGAAGTCAACACGTCGGATCTCCTGGATTACATGCGATCCCGTCCGCACTCGGCTTTCTCTAGGAAGG CGAGAGAGTGCATGATTTCTGTCGCCATCTGCCATACCTGTCTGCCCGAACACAAGGACGGCAGTATCGAGTACC AGGCATCGTCACCCGATGAGCTGGCCCTAGTGAAGGCGTCACAGGAACTCGGCTACCAGGTGACGAACCGCACGT CGCAATCCATGACCCTGCAGGTCCCGCGGCCGAATGGCCAGGTCGATAAGATGGTCTTCCAGATCTTGGATGTGA TTGAGTTCAGCAGTACGCGCAAGAGAATGTCCATCATCGTCCGCTATCCCGACGGGCGCATCTCCCTCATTTGCA AGGGCGCCGATTCGGCTATCCTGCCACGACTGAAACTTTCCTCGCTGGCCATGCAAAAGGCAGGCGAGGTCCGCA AGAGTGCCGATCTCGAGCGCGAGATGCATCGCCGTAGTGAGCAGCAGGAGCCCCGGAATAGCTTTGGCGGGAGGC CGAGCCTGACCGTCCATCGCAACCACGGAGTTATGAGGGACGCGAGCTTGAGTCGGCGGCCGGTCGCCAGCAGAA GCAAGTCGTTCGAGATTAACAAGCTCGCCCGATCGTCCGTCGACCGAGTTCGAGTCTCGCTCTCCTCCCCGCGCG GCGCCTCACTCGATGTGTCGCGCGCTCAGTTTGCGAATCCGCCAGCTCTCCACTCGCGGTCCGCGCATGATCGCA TGGATTTCCTGGACGACCCCTCCATCTTCGACGAGTCGGAAGTCTTCACAAGGTGTTTCAAGCACATCGACGACT TTGCAACAGAGGGCCTCCGGACGCTGATCTACGCTCAAAAGTTCATCTCGGAGCAGGAGTATATTGAGTGGAAAG GGCTCTACGACGAAGCGACGACGAGCCTCGACAACCGGCAGGAGATGATTGAAGCCGCCGGAGAAAAGATTGAGC AGTCGTTCGACCTCGTCGGTGCCACCGCTATCGAGGACAAACTTCAGCGTGGCGTGCCCGAGACTATCGACAAGC TGCGACGTGCCAACATCAGGATATGGATGCTCACTGGCGACAAGCGCGAAACGGCCATCAACATTGCTCATTCGG CGCGCATATGCCGGCCCGCTTCGGATCTGTTCGTCCTGGACGCGACCAAGGGCTCTCTATGGTCGCAGCTCGCTG CCTTGGCCGAAGACCTGCAAGAGGGTTCCGTCCACAGCGTCATGGTCGTCGACGGGCAGACTCTGGCAGCCGTGG AGAAGTCGGCCGAGCTATCACAGAGGTTTTTTGACCTCGCCGTTCTCGTCGACTCCGTCATATGCTGCCGGGCCG CGCCGGCCCAGAAGGCGTTATTGGTGCGGGCTGTGCGCTCTCGCCTGTGTGCTGCCAAGGGAAAGCATCGCCACG GGTTGACGCTGGCCATTGGCGATGGCGCAAACGACATCGCCATGATCCAAGAAAGTCACGTTGGCATAGGAATCT CGGGACAGGAGGGCCTGCAGGCGGCGCGCATCGCCGACTACTCCATAGCGCAGTTCCGGTTTCTGCAGAGGATGC TCCTCGTCCACGGGCGCTGGAACTACATCCGGACCGCAAAGTTCATCCTCTGCACCTTCTGGAAAGAGCTGTTTT TCTATCTCCCGGCCGCACAGTTCCAAAGACTTAATGGTTACAGCGGCACCTCGCTGTTCCAGGAGACGAGCCTGA CCGTCTTCAACACGCTCTTCACCAGTCTCTGCACCATCTGTATGGGCATCTGGGAGCAGGACCTGAGAGCCGAAA CGCTGCTCGCCGTGCCGGAGCTCTACGTGTACGGGCAGCGCGACCTGGGGCTGAACATGAGCAAATATCTGCGCT GGATGTTCCTGGCATGCGTGGAAGGCGTCATTGTCTTTCACGGCGCCTGGGCAGGCTACGGATTGATCGAGCCGG GCATCCGCGACTCGGGTCTGTACCCCCTGGGGACGCTCGTCTTCACGTTGGCGGTCTTCTGGATCAACTGGAAGC TACTGTGAGTTGGACGGACGGACGGGAGAGGAGACGACGAGACTGACGGCGCGGCAGCATTTTCGAGACGCACTA CAAGACGGCCATCGTCATCGGCTCCTTCTTCCTCACGACCGTGGGCTGGTGGGCCTGGCTCTCCTTCCTCGACGA AGTCTTCCCGCTGATGCCTTCGGGGCCCAACGCCGTCCACGACTCGTTCACCAAGCACTGGGGCCAGGACGCAGC CTGGTGGGCGACGGTCTTCCTCGTCCTCACCGTCCTCGGCGCGATCGGGGCCTGTGGCAAGGTGGTCAAGCGGCA GATGCTCCTGGCCGGCTTCTGGCAGTGGCCGCCGTGGCGGAGACGGCGGAGGCTGAGCGACAATGTGGAGGAGTG GGACCTGGAGCTGTGGCAGGAGCTGGAGCAGGACCCGGTCGTGCGCGAGCAGCTGAGGGCCCTGGCCCGGGACGA GGGCTCGCCGGCCGACGAGGCGGCGGCCGCGGAGGACGGGGCCGAGCCCGGGACGGCCACGGCCAAGGCCTGA |