© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|6991 |
| Gene name | |
| Location | Contig_384:14827..19688 |
| Strand | + |
| Gene length (bp) | 4861 |
| Transcript length (bp) | 4638 |
| Coding sequence length (bp) | 4638 |
| Protein length (aa) | 1546 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF16212 | PhoLip_ATPase_C | Phospholipid-translocating P-type ATPase C-terminal | 1.2E-77 | 1114 | 1363 |
| PF16209 | PhoLip_ATPase_N | Phospholipid-translocating ATPase N-terminal | 2.0E-18 | 115 | 164 |
| PF13246 | Cation_ATPase | Cation transport ATPase (P-type) | 5.1E-14 | 760 | 843 |
| PF00702 | Hydrolase | haloacid dehalogenase-like hydrolase | 8.5E-08 | 630 | 996 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P32660|ATC5_YEAST | Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 | 94 | 1389 | 0.0E+00 |
| sp|Q12675|ATC4_YEAST | Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 | 94 | 1378 | 0.0E+00 |
| sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 94 | 1374 | 0.0E+00 |
| sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 82 | 1372 | 0.0E+00 |
| sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 304 | 1371 | 0.0E+00 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P32660|ATC5_YEAST | Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 | 94 | 1389 | 0.0E+00 |
| sp|Q12675|ATC4_YEAST | Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 | 94 | 1378 | 0.0E+00 |
| sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 94 | 1374 | 0.0E+00 |
| sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 82 | 1372 | 0.0E+00 |
| sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 304 | 1371 | 0.0E+00 |
| sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 311 | 1374 | 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 | 355 | 1374 | 0.0E+00 |
| sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 351 | 1374 | 0.0E+00 |
| sp|Q9SX33|ALA9_ARATH | Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 | 311 | 1363 | 0.0E+00 |
| sp|P98198|AT8B2_HUMAN | Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 | 355 | 1370 | 0.0E+00 |
| sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 351 | 1374 | 0.0E+00 |
| sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 353 | 1374 | 0.0E+00 |
| sp|P98199|AT8B2_MOUSE | Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 | 355 | 1370 | 0.0E+00 |
| sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 360 | 1377 | 0.0E+00 |
| sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 360 | 1377 | 0.0E+00 |
| sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 353 | 1367 | 0.0E+00 |
| sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 360 | 1377 | 0.0E+00 |
| sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 355 | 1363 | 0.0E+00 |
| sp|Q9LNQ4|ALA4_ARATH | Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 | 328 | 1371 | 0.0E+00 |
| sp|Q9LI83|ALA10_ARATH | Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 | 355 | 1363 | 0.0E+00 |
| sp|P98200|AT8A2_MOUSE | Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 | 360 | 1356 | 0.0E+00 |
| sp|O94296|YOOC_SCHPO | Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 | 351 | 1374 | 0.0E+00 |
| sp|Q9SGG3|ALA5_ARATH | Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 | 355 | 1377 | 0.0E+00 |
| sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 359 | 1356 | 0.0E+00 |
| sp|P57792|ALA12_ARATH | Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 | 311 | 1374 | 0.0E+00 |
| sp|Q9LVK9|ALA7_ARATH | Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 | 355 | 1371 | 0.0E+00 |
| sp|Q9NTI2|AT8A2_HUMAN | Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 | 360 | 1356 | 0.0E+00 |
| sp|Q9SLK6|ALA6_ARATH | Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 | 355 | 1371 | 0.0E+00 |
| sp|P98204|ALA1_ARATH | Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 | 354 | 1378 | 0.0E+00 |
| sp|A3FIN4|AT8B5_MOUSE | Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 | 323 | 1367 | 0.0E+00 |
| sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 340 | 1331 | 0.0E+00 |
| sp|O60423|AT8B3_HUMAN | Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 | 352 | 1375 | 5.0E-180 |
| sp|Q9Y2G3|AT11B_HUMAN | Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 | 361 | 1349 | 2.0E-177 |
| sp|Q9N0Z4|AT11B_RABIT | Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 | 361 | 1349 | 9.0E-171 |
| sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 360 | 1363 | 1.0E-169 |
| sp|P98196|AT11A_HUMAN | Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 | 351 | 1363 | 2.0E-163 |
| sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 351 | 1381 | 2.0E-161 |
| sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 354 | 1360 | 1.0E-156 |
| sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 354 | 1360 | 2.0E-155 |
| sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 751 | 1409 | 1.0E-136 |
| sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 758 | 1358 | 5.0E-134 |
| sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 759 | 1409 | 9.0E-134 |
| sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 750 | 1366 | 2.0E-130 |
| sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 750 | 1402 | 2.0E-129 |
| sp|Q9GKS6|AT10D_MACFA | Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 | 760 | 1360 | 7.0E-127 |
| sp|O70228|ATP9A_MOUSE | Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 | 362 | 1363 | 4.0E-101 |
| sp|O75110|ATP9A_HUMAN | Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 | 362 | 1363 | 2.0E-100 |
| sp|F1Q4S1|ATP9B_DANRE | Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 | 363 | 1363 | 7.0E-99 |
| sp|A1A4J6|ATP9B_BOVIN | Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 | 363 | 1363 | 1.0E-98 |
| sp|P98195|ATP9B_MOUSE | Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 | 363 | 1363 | 7.0E-98 |
| sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 674 | 1376 | 3.0E-97 |
| sp|D4ABB8|ATP9B_RAT | Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 | 363 | 1363 | 2.0E-96 |
| sp|O43861|ATP9B_HUMAN | Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 | 363 | 1363 | 3.0E-96 |
| sp|P40527|ATC7_YEAST | Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 | 361 | 1363 | 3.0E-96 |
| sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 359 | 1249 | 3.0E-94 |
| sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 835 | 1396 | 2.0E-79 |
| sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 855 | 1374 | 2.0E-73 |
| sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 361 | 844 | 9.0E-66 |
| sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 321 | 657 | 2.0E-63 |
| sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 321 | 657 | 9.0E-63 |
| sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 360 | 659 | 6.0E-60 |
| sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 360 | 657 | 1.0E-59 |
| sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 321 | 766 | 3.0E-59 |
| sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 360 | 657 | 4.0E-45 |
| sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 361 | 665 | 2.0E-37 |
| sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 738 | 847 | 8.0E-19 |
| sp|Q08853|ATC_PLAFK | Calcium-transporting ATPase OS=Plasmodium falciparum (isolate K1 / Thailand) GN=ATP6 PE=3 SV=1 | 805 | 1161 | 2.0E-18 |
| sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 119 | 199 | 1.0E-16 |
| sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 115 | 199 | 1.0E-16 |
| sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 115 | 199 | 2.0E-16 |
| sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 119 | 199 | 1.0E-14 |
| sp|P98204|ALA1_ARATH | Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 | 74 | 215 | 4.0E-14 |
| sp|O74431|ATC9_SCHPO | Probable cation-transporting ATPase C1672.11c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPCC1672.11c PE=3 SV=1 | 804 | 1114 | 9.0E-14 |
| sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 73 | 234 | 2.0E-13 |
| sp|P23634|AT2B4_HUMAN | Plasma membrane calcium-transporting ATPase 4 OS=Homo sapiens GN=ATP2B4 PE=1 SV=2 | 794 | 1150 | 2.0E-13 |
| sp|P98196|AT11A_HUMAN | Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 | 116 | 207 | 3.0E-13 |
| sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 116 | 207 | 4.0E-13 |
| sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 73 | 215 | 1.0E-12 |
| sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 73 | 215 | 1.0E-12 |
| sp|Q9Y2G3|AT11B_HUMAN | Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 | 86 | 218 | 1.0E-12 |
| sp|Q9N0Z4|AT11B_RABIT | Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 | 86 | 218 | 1.0E-12 |
| sp|Q27533|YH2M_CAEEL | Probable cation-transporting ATPase W08D2.5 OS=Caenorhabditis elegans GN=W08D2.5 PE=3 SV=2 | 801 | 1191 | 2.0E-12 |
| sp|Q2QMX9|ACA1_ORYSJ | Calcium-transporting ATPase 1, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os12g0586600 PE=2 SV=1 | 766 | 1000 | 4.0E-12 |
| sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 116 | 201 | 5.0E-12 |
| sp|Q6Q477|AT2B4_MOUSE | Plasma membrane calcium-transporting ATPase 4 OS=Mus musculus GN=Atp2b4 PE=1 SV=1 | 794 | 989 | 5.0E-12 |
| sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 114 | 213 | 9.0E-12 |
| sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 116 | 202 | 1.0E-11 |
| sp|Q21286|YBF7_CAEEL | Probable cation-transporting ATPase K07E3.7 OS=Caenorhabditis elegans GN=K07E3.7/K07E3.6 PE=3 SV=4 | 717 | 1114 | 1.0E-11 |
| sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 92 | 225 | 2.0E-11 |
| sp|Q9SGG3|ALA5_ARATH | Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 | 83 | 213 | 2.0E-11 |
| sp|P57792|ALA12_ARATH | Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 | 119 | 215 | 2.0E-11 |
| sp|Q9LVK9|ALA7_ARATH | Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 | 113 | 204 | 2.0E-11 |
| sp|Q9SLK6|ALA6_ARATH | Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 | 116 | 204 | 2.0E-11 |
| sp|A3FIN4|AT8B5_MOUSE | Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 | 111 | 213 | 2.0E-11 |
| sp|Q12697|YPK9_YEAST | Vacuolar cation-transporting ATPase YPK9 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YPK9 PE=1 SV=1 | 615 | 1114 | 2.0E-11 |
| sp|D3K0R6|AT2B4_BOVIN | Plasma membrane calcium-transporting ATPase 4 OS=Bos taurus GN=ATP2B4 PE=1 SV=2 | 798 | 1150 | 3.0E-11 |
| sp|Q9R0K7|AT2B2_MOUSE | Plasma membrane calcium-transporting ATPase 2 OS=Mus musculus GN=Atp2b2 PE=1 SV=2 | 796 | 987 | 3.0E-11 |
| sp|Q9NQ11|AT132_HUMAN | Probable cation-transporting ATPase 13A2 OS=Homo sapiens GN=ATP13A2 PE=1 SV=2 | 804 | 1110 | 3.0E-11 |
| sp|Q16720|AT2B3_HUMAN | Plasma membrane calcium-transporting ATPase 3 OS=Homo sapiens GN=ATP2B3 PE=1 SV=3 | 798 | 987 | 3.0E-11 |
| sp|Q64568|AT2B3_RAT | Plasma membrane calcium-transporting ATPase 3 OS=Rattus norvegicus GN=Atp2b3 PE=1 SV=2 | 803 | 987 | 3.0E-11 |
| sp|P11506|AT2B2_RAT | Plasma membrane calcium-transporting ATPase 2 OS=Rattus norvegicus GN=Atp2b2 PE=1 SV=2 | 796 | 983 | 4.0E-11 |
| sp|Q6ATV4|ACA2_ORYSJ | Calcium-transporting ATPase 2, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os03g0616400 PE=2 SV=1 | 803 | 968 | 5.0E-11 |
| sp|Q4VNC1|AT134_HUMAN | Probable cation-transporting ATPase 13A4 OS=Homo sapiens GN=ATP13A4 PE=2 SV=3 | 741 | 1114 | 7.0E-11 |
| sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 119 | 228 | 8.0E-11 |
| sp|Q9LI83|ALA10_ARATH | Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 | 88 | 225 | 8.0E-11 |
| sp|Q9LNQ4|ALA4_ARATH | Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 | 67 | 213 | 9.0E-11 |
| sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 116 | 231 | 9.0E-11 |
| sp|Q01814|AT2B2_HUMAN | Plasma membrane calcium-transporting ATPase 2 OS=Homo sapiens GN=ATP2B2 PE=1 SV=2 | 796 | 987 | 9.0E-11 |
| sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 116 | 218 | 2.0E-10 |
| sp|P58165|AT2B2_OREMO | Plasma membrane calcium-transporting ATPase 2 (Fragment) OS=Oreochromis mossambicus GN=atp2b2 PE=2 SV=1 | 794 | 966 | 2.0E-10 |
| sp|O94296|YOOC_SCHPO | Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 | 103 | 232 | 3.0E-10 |
| sp|Q9SX33|ALA9_ARATH | Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 | 115 | 204 | 4.0E-10 |
| sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 119 | 202 | 8.0E-10 |
| sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 72 | 213 | 1.0E-09 |
| sp|Q5XF90|AT134_MOUSE | Probable cation-transporting ATPase 13A4 OS=Mus musculus GN=Atp13a4 PE=2 SV=1 | 741 | 1114 | 1.0E-09 |
| sp|Q9NTI2|AT8A2_HUMAN | Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 | 85 | 215 | 2.0E-09 |
| sp|Q9LF79|ACA8_ARATH | Calcium-transporting ATPase 8, plasma membrane-type OS=Arabidopsis thaliana GN=ACA8 PE=1 SV=1 | 766 | 971 | 2.0E-09 |
| sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 85 | 198 | 3.0E-09 |
| sp|O60423|AT8B3_HUMAN | Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 | 116 | 205 | 5.0E-09 |
| sp|P23220|AT2B1_PIG | Plasma membrane calcium-transporting ATPase 1 OS=Sus scrofa GN=ATP2B1 PE=2 SV=1 | 794 | 1150 | 5.0E-09 |
| sp|P20020|AT2B1_HUMAN | Plasma membrane calcium-transporting ATPase 1 OS=Homo sapiens GN=ATP2B1 PE=1 SV=3 | 794 | 1150 | 5.0E-09 |
| sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 116 | 213 | 7.0E-09 |
| sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 109 | 215 | 9.0E-09 |
| sp|P98200|AT8A2_MOUSE | Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 | 116 | 215 | 1.0E-08 |
| sp|G5E829|AT2B1_MOUSE | Plasma membrane calcium-transporting ATPase 1 OS=Mus musculus GN=Atp2b1 PE=1 SV=1 | 794 | 1150 | 1.0E-08 |
| sp|P11505|AT2B1_RAT | Plasma membrane calcium-transporting ATPase 1 OS=Rattus norvegicus GN=Atp2b1 PE=1 SV=2 | 794 | 1150 | 1.0E-08 |
| sp|Q64542|AT2B4_RAT | Plasma membrane calcium-transporting ATPase 4 OS=Rattus norvegicus GN=Atp2b4 PE=1 SV=1 | 796 | 989 | 1.0E-08 |
| sp|Q9CTG6|AT132_MOUSE | Probable cation-transporting ATPase 13A2 OS=Mus musculus GN=Atp13a2 PE=2 SV=3 | 804 | 1110 | 2.0E-08 |
| sp|O22218|ACA4_ARATH | Calcium-transporting ATPase 4, plasma membrane-type OS=Arabidopsis thaliana GN=ACA4 PE=1 SV=1 | 798 | 964 | 3.0E-08 |
| sp|P98198|AT8B2_HUMAN | Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 | 114 | 213 | 4.0E-08 |
| sp|Q9LU41|ACA9_ARATH | Calcium-transporting ATPase 9, plasma membrane-type OS=Arabidopsis thaliana GN=ACA9 PE=2 SV=2 | 742 | 1043 | 6.0E-08 |
| sp|P98199|AT8B2_MOUSE | Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 | 114 | 213 | 1.0E-07 |
| sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 116 | 208 | 2.0E-07 |
| sp|P39986|ATC6_YEAST | Manganese-transporting ATPase 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SPF1 PE=1 SV=1 | 804 | 1105 | 2.0E-07 |
| sp|Q5XF89|AT133_MOUSE | Probable cation-transporting ATPase 13A3 OS=Mus musculus GN=Atp13a3 PE=1 SV=1 | 804 | 1114 | 2.0E-07 |
| sp|Q00804|AT2B1_RABIT | Plasma membrane calcium-transporting ATPase 1 OS=Oryctolagus cuniculus GN=ATP2B1 PE=2 SV=2 | 794 | 989 | 3.0E-07 |
| sp|O70228|ATP9A_MOUSE | Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 | 110 | 218 | 4.0E-07 |
| sp|O75110|ATP9A_HUMAN | Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 | 110 | 218 | 4.0E-07 |
| sp|O14022|CTA5_SCHPO | Cation-transporting ATPase 5 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=cta5 PE=3 SV=1 | 797 | 1114 | 4.0E-07 |
| sp|Q9SZR1|ACA10_ARATH | Calcium-transporting ATPase 10, plasma membrane-type OS=Arabidopsis thaliana GN=ACA10 PE=1 SV=2 | 810 | 986 | 5.0E-07 |
| sp|Q2QY12|ACA4_ORYSJ | Probable calcium-transporting ATPase 4, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os12g0136900 PE=3 SV=1 | 810 | 968 | 7.0E-07 |
| sp|P39524|ATC3_YEAST | Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 | 85 | 200 | 1.0E-06 |
| sp|Q9LT02|PDR2_ARATH | Probable manganese-transporting ATPase PDR2 OS=Arabidopsis thaliana GN=PDR2 PE=1 SV=1 | 797 | 1105 | 1.0E-06 |
| sp|Q9CFU9|LLCA1_LACLA | Calcium-transporting ATPase 1 OS=Lactococcus lactis subsp. lactis (strain IL1403) GN=yoaB PE=1 SV=1 | 810 | 980 | 2.0E-06 |
| sp|Q2RAS0|ACA5_ORYSJ | Probable calcium-transporting ATPase 5, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os11g0140400 PE=3 SV=1 | 810 | 968 | 3.0E-06 |
| sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 116 | 199 | 5.0E-06 |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 28 | 0.45 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 146 | 180 | 34 |
| 2 | 521 | 543 | 22 |
| 3 | 567 | 589 | 22 |
| 4 | 1149 | 1166 | 17 |
| 5 | 1176 | 1198 | 22 |
| 6 | 1229 | 1251 | 22 |
| 7 | 1266 | 1288 | 22 |
| 8 | 1295 | 1317 | 22 |
| 9 | 1327 | 1349 | 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|6991 MSSPPRAPLEPGPDQKIEHTQRARWATRKLTVRSGRIKRLSLLNRGQHRRAGSNEKDSGQGDPNEPPLADLPDGG ESHDIVSDSGDSQDDSTNRTLYFNLPLPDDLLEDGHPIYSFPRNKIRTAKYTPLSFVPKNLWFQFHNVANIFFLF LVILVIFPIFGGVNPGLNAVPLIFIIVVTAIKDAIEDYRRTILDIELNNAPVHRLHHWNNVNVEEDNVSSWRRFK KANSTFFGSIWRAIESLWSKKARTARAERKERKLNPPGEEEGRPSVETVRTRRSMREALASPFNRDSFMSANDEI REEIQMTPVPSPTPPNNAPRIVLPDDSQDVKRAAAVQSMKSDLINYQRGPQGARFKKDAWKSLQVGDFVRIYNDD ELPADVIILSTSDPDGACYVETKNLDGETNLKVRQALRCGRSLKHARDCERAEFRIESEPPQPNLYKYNGAIRWE QPVPGYADDDPEEMTEPITIDNLLLRGCNLRNTEWVLGVVIFTGHETKIMMNAGITPSKRARIAREMNFNVICNF GILLIMCLLSAIVNGVAWARTDASLHFFEFGAIGGSAPVSGFITFWAAIIVFQNLVPISLYITLEIVRTLQAIFI FSDVEMYYEKIDQPCIPKSWNISDDVGQIEYIFSDKTGTLTQNVMEFKKATINGQPYGEAFTEAQAGMQKRMGVD IETEGARIRAEIAEAKVRALGGLRKINKNPYLHDDDVTFIAPDFVSDLAGDSGPEQKAANAEFMLALALCHTVIA ERTPGDPPKMNFKAQSPDEEALVATARDMGFTVLGNSGDGINLNVMGEERHYQILNTIEFNSSRKRMSSIVRMPN GQIVLYCKGADSVIYARLKRGEQQQLRRETAEHLEMFAREGLRTLCIASKVLTEREYKVWKKEHDAAAAALEHRE EKLEEVAELIEQDLLLLGGTAIEDRLQDGVPDTIALLGQAGIKLWVLTGDKVETAINIGFSCNLLNNDMELIHLK VDEDESGETSDDSFLETVGKLLDQHLATFGIAGNDEDLALAKKNHEPPAPTHGLVIDGFTLRWALHDALKQKFLL LCKQCKSVLCCRVSPAQKAAVVAMVKNGLDVMTLSIGDGANDVAMIQEADVGVGIAGVEGRQAAMSSDYAIAQFR FLQRLVLVHGRWSYRRLAESISNFFYKNMVWTFSIFWFEIFCDFDITYLFDYTYILMFNLFFTSLPVGIMGVLDQ DVSDKVSLAVPELYRRGIERLEWTQRKFWLYMIDGVYQSVMVFFIPYLLFIHGRSVSFSGLGLEDRLRFGAYVAH PAVLTINGYILINTYRWDWLMVLIVVISDLFIFFWTGVYTSFTGSDFFYKAAAQVYGEASFWAIFFIVPIICLFP RFAIKSLQKVYWPYDVDIIREQEKMGQFAYLNAAAGPEEIKVKSNDEKSQKSSESANKTQHVAYGSVDEDLRPIY PPSTATRTTHNHTQHGSDSTNYTANRMSIEVAPVNRLSSDAPAHTRPSIDRARPSIDRARPSYDRMRMSMDRCRP SYEASSDFTTAARLTRIESSQTGAAQGIKARLRGLSLSKNANNQS* |
| Coding | >Hirsu2|6991 ATGTCCTCCCCCCCCCGCGCGCCACTCGAGCCCGGCCCCGACCAGAAGATCGAGCACACGCAGAGGGCACGCTGG GCCACCCGCAAGCTGACCGTCAGGAGCGGCCGCATCAAGCGCCTGTCGCTCCTCAACCGCGGCCAGCACCGGCGC GCCGGCTCCAACGAGAAGGACTCGGGCCAAGGCGACCCCAACGAACCGCCCTTGGCCGACCTCCCCGACGGCGGC GAGAGCCATGACATCGTGTCCGACTCGGGCGATTCGCAAGACGACAGCACCAACCGCACCCTCTACTTCAACCTC CCCCTGCCCGACGACTTGCTCGAAGACGGCCACCCCATATACTCCTTTCCTCGGAACAAGATCAGGACAGCAAAG TACACGCCGCTCTCCTTCGTCCCCAAGAACCTGTGGTTCCAGTTCCACAATGTCGCCAACATCTTCTTCCTCTTT CTCGTCATTCTTGTCATATTCCCCATCTTCGGCGGCGTCAACCCCGGGCTCAATGCCGTCCCCCTCATCTTCATC ATCGTCGTCACCGCCATCAAAGACGCCATCGAGGACTACCGCCGAACCATACTCGACATCGAGCTCAACAACGCT CCCGTGCACCGCCTGCACCACTGGAACAATGTCAACGTCGAGGAGGACAACGTGTCTTCGTGGAGGAGGTTCAAG AAGGCAAACTCCACCTTCTTCGGCTCCATCTGGCGCGCCATCGAGAGCCTGTGGTCCAAGAAGGCCCGGACGGCT CGCGCCGAGCGCAAGGAACGCAAGCTGAACCCGCCCGGCGAAGAAGAGGGCCGACCCTCGGTAGAGACGGTGCGC ACCAGGCGCTCGATGCGAGAGGCGCTCGCCTCGCCCTTCAACCGCGACTCCTTCATGTCGGCCAATGACGAGATC CGCGAAGAGATCCAGATGACGCCCGTGCCGTCGCCCACCCCGCCCAACAACGCGCCTCGCATCGTGCTGCCCGAC GACAGTCAGGACGTTAAGCGCGCCGCCGCCGTGCAGTCGATGAAGTCGGATCTCATCAACTACCAACGTGGTCCC CAGGGGGCCCGCTTCAAAAAGGACGCCTGGAAGAGCCTGCAGGTGGGCGACTTCGTCCGAATCTACAACGACGAC GAGCTGCCCGCAGACGTCATCATCCTCTCCACCTCGGACCCCGACGGCGCCTGTTACGTCGAGACGAAGAACCTG GACGGCGAGACGAACCTCAAGGTTCGCCAGGCCCTGCGCTGCGGCCGATCCCTCAAGCACGCGCGCGACTGCGAG CGGGCCGAGTTCCGCATCGAGAGCGAGCCCCCGCAGCCCAACCTCTACAAGTACAACGGCGCCATACGGTGGGAG CAGCCCGTGCCCGGCTACGCCGACGACGACCCCGAGGAGATGACGGAGCCCATCACCATCGACAACCTCCTGCTC CGCGGCTGCAACCTGAGGAACACGGAGTGGGTGCTGGGCGTCGTCATCTTCACCGGCCACGAGACCAAGATCATG ATGAACGCCGGCATCACGCCCAGCAAGCGCGCCAGGATCGCCCGCGAGATGAACTTCAACGTCATCTGCAACTTT GGCATCCTCCTTATCATGTGCCTGCTCTCGGCCATCGTCAACGGCGTCGCCTGGGCGAGGACCGACGCCTCGCTG CACTTCTTCGAGTTCGGCGCCATTGGCGGCAGCGCGCCCGTGAGCGGCTTCATCACCTTCTGGGCCGCCATCATC GTCTTCCAGAACCTGGTGCCCATCTCCCTCTACATCACGCTCGAGATCGTCCGCACGCTCCAGGCCATCTTCATC TTCAGCGACGTCGAGATGTACTACGAGAAGATCGACCAGCCGTGCATCCCCAAGTCGTGGAACATCTCCGACGAC GTCGGCCAGATCGAGTACATCTTCTCCGACAAGACCGGCACCCTCACGCAAAACGTCATGGAGTTCAAGAAGGCC ACCATCAACGGCCAGCCGTACGGCGAGGCCTTCACGGAGGCCCAGGCCGGGATGCAGAAGAGGATGGGCGTCGAC ATCGAGACCGAGGGCGCCAGGATCCGCGCCGAGATTGCCGAGGCCAAGGTCCGGGCCCTGGGCGGCCTGCGCAAG ATCAACAAGAACCCCTACCTCCACGACGACGACGTCACCTTCATCGCCCCGGACTTCGTCTCCGACCTCGCCGGC GACTCCGGGCCCGAGCAGAAGGCGGCCAACGCCGAGTTCATGCTGGCGTTGGCGCTGTGCCACACCGTCATCGCC GAGAGGACGCCCGGCGATCCTCCCAAGATGAATTTCAAGGCGCAGTCGCCCGACGAGGAAGCCCTCGTCGCCACG GCCCGGGACATGGGCTTCACCGTCCTGGGCAATTCCGGCGACGGCATCAACCTCAACGTCATGGGCGAGGAGCGC CACTACCAGATCCTCAACACCATCGAGTTCAACTCGAGCCGGAAGCGGATGAGCTCCATCGTCCGGATGCCAAAC GGCCAGATCGTCCTCTACTGCAAGGGTGCCGACTCCGTCATCTACGCGCGACTGAAGAGGGGCGAGCAGCAGCAG CTCAGGCGGGAGACGGCCGAGCATCTCGAGATGTTCGCCCGGGAAGGCCTGCGGACGCTCTGCATCGCGAGCAAG GTCTTGACGGAGCGCGAGTACAAGGTGTGGAAGAAGGAGCACGACGCTGCCGCCGCGGCGCTCGAGCACCGCGAG GAGAAGCTGGAGGAGGTGGCGGAGCTCATCGAGCAGGACCTGCTGCTGCTGGGCGGAACGGCCATCGAGGATCGG CTGCAAGACGGCGTGCCCGACACCATTGCCCTACTGGGCCAGGCCGGCATCAAGCTCTGGGTCCTGACGGGTGAC AAGGTCGAGACGGCCATCAACATCGGCTTCTCCTGCAACCTGCTCAACAACGACATGGAGCTGATCCACCTCAAG GTCGACGAGGACGAGTCGGGCGAGACCAGCGACGACAGCTTCCTCGAGACGGTCGGCAAGCTGCTCGACCAACAC CTGGCGACGTTCGGAATCGCCGGCAACGACGAAGACCTCGCCCTGGCCAAGAAGAACCACGAACCGCCGGCGCCC ACGCACGGCCTCGTCATCGACGGCTTCACCCTCCGCTGGGCCCTGCACGACGCCCTGAAGCAAAAGTTCCTCCTG CTGTGCAAGCAGTGCAAGTCCGTGCTGTGCTGCCGCGTGAGCCCCGCGCAGAAGGCGGCCGTCGTGGCCATGGTC AAGAACGGCCTGGACGTCATGACCCTGTCCATCGGCGACGGGGCCAACGACGTGGCCATGATCCAGGAGGCCGAT GTTGGCGTGGGCATTGCCGGCGTCGAGGGCCGCCAGGCCGCTATGTCGTCGGACTATGCCATCGCTCAGTTCCGC TTCCTGCAGAGGCTGGTGCTGGTGCACGGCCGCTGGTCCTACCGCCGTCTGGCCGAGAGCATCAGCAACTTCTTC TACAAGAACATGGTCTGGACCTTTAGCATCTTCTGGTTCGAGATCTTCTGCGACTTCGACATCACCTACCTCTTC GACTACACCTACATCCTTATGTTCAACCTCTTCTTCACCTCGCTGCCCGTCGGCATCATGGGCGTGCTCGACCAG GACGTCTCGGACAAGGTTTCGCTCGCCGTTCCCGAGCTGTACCGACGGGGCATCGAGCGGCTCGAGTGGACCCAG CGCAAGTTCTGGCTGTACATGATTGACGGCGTCTACCAATCCGTCATGGTCTTCTTCATCCCCTACCTGCTCTTC ATCCACGGCCGGTCCGTGTCGTTTTCCGGACTGGGCCTCGAGGACAGGCTGCGCTTCGGCGCCTACGTCGCGCAT CCCGCCGTGCTGACCATCAACGGGTACATCCTGATCAACACGTACCGCTGGGACTGGCTGATGGTCCTCATCGTC GTCATCAGCGACCTGTTCATCTTCTTCTGGACCGGCGTCTACACCTCCTTCACCGGGTCCGACTTCTTCTACAAG GCGGCCGCCCAGGTGTACGGCGAGGCCAGCTTCTGGGCCATCTTCTTCATCGTGCCCATCATCTGCCTGTTCCCG CGGTTCGCCATCAAATCGCTGCAGAAGGTGTACTGGCCGTACGACGTCGACATCATCCGAGAGCAGGAGAAGATG GGCCAGTTCGCCTACCTCAATGCCGCAGCCGGGCCGGAGGAGATCAAGGTGAAGAGCAACGACGAGAAGAGCCAG AAGTCGTCGGAAAGCGCCAACAAGACCCAGCACGTGGCCTACGGCAGCGTGGACGAGGACCTGCGTCCCATCTAC CCGCCGTCGACGGCGACGCGGACGACGCACAACCACACGCAGCACGGCAGCGACTCGACCAACTACACGGCCAAC CGCATGTCGATCGAGGTGGCGCCGGTCAACCGCCTGTCGTCGGACGCGCCGGCACACACGCGGCCGTCGATCGAT AGGGCCAGGCCGTCGATCGACAGGGCCAGGCCGTCGTACGACCGGATGCGCATGTCCATGGACCGCTGCCGGCCC AGCTACGAGGCCAGCAGCGACTTCACGACGGCGGCACGGCTGACGCGCATCGAGTCCAGCCAAACGGGCGCCGCC CAAGGGATCAAGGCAAGGCTACGAGGCCTGTCGTTGAGCAAGAATGCCAACAACCAGTCGTAA |
| Transcript | >Hirsu2|6991 ATGTCCTCCCCCCCCCGCGCGCCACTCGAGCCCGGCCCCGACCAGAAGATCGAGCACACGCAGAGGGCACGCTGG GCCACCCGCAAGCTGACCGTCAGGAGCGGCCGCATCAAGCGCCTGTCGCTCCTCAACCGCGGCCAGCACCGGCGC GCCGGCTCCAACGAGAAGGACTCGGGCCAAGGCGACCCCAACGAACCGCCCTTGGCCGACCTCCCCGACGGCGGC GAGAGCCATGACATCGTGTCCGACTCGGGCGATTCGCAAGACGACAGCACCAACCGCACCCTCTACTTCAACCTC CCCCTGCCCGACGACTTGCTCGAAGACGGCCACCCCATATACTCCTTTCCTCGGAACAAGATCAGGACAGCAAAG TACACGCCGCTCTCCTTCGTCCCCAAGAACCTGTGGTTCCAGTTCCACAATGTCGCCAACATCTTCTTCCTCTTT CTCGTCATTCTTGTCATATTCCCCATCTTCGGCGGCGTCAACCCCGGGCTCAATGCCGTCCCCCTCATCTTCATC ATCGTCGTCACCGCCATCAAAGACGCCATCGAGGACTACCGCCGAACCATACTCGACATCGAGCTCAACAACGCT CCCGTGCACCGCCTGCACCACTGGAACAATGTCAACGTCGAGGAGGACAACGTGTCTTCGTGGAGGAGGTTCAAG AAGGCAAACTCCACCTTCTTCGGCTCCATCTGGCGCGCCATCGAGAGCCTGTGGTCCAAGAAGGCCCGGACGGCT CGCGCCGAGCGCAAGGAACGCAAGCTGAACCCGCCCGGCGAAGAAGAGGGCCGACCCTCGGTAGAGACGGTGCGC ACCAGGCGCTCGATGCGAGAGGCGCTCGCCTCGCCCTTCAACCGCGACTCCTTCATGTCGGCCAATGACGAGATC CGCGAAGAGATCCAGATGACGCCCGTGCCGTCGCCCACCCCGCCCAACAACGCGCCTCGCATCGTGCTGCCCGAC GACAGTCAGGACGTTAAGCGCGCCGCCGCCGTGCAGTCGATGAAGTCGGATCTCATCAACTACCAACGTGGTCCC CAGGGGGCCCGCTTCAAAAAGGACGCCTGGAAGAGCCTGCAGGTGGGCGACTTCGTCCGAATCTACAACGACGAC GAGCTGCCCGCAGACGTCATCATCCTCTCCACCTCGGACCCCGACGGCGCCTGTTACGTCGAGACGAAGAACCTG GACGGCGAGACGAACCTCAAGGTTCGCCAGGCCCTGCGCTGCGGCCGATCCCTCAAGCACGCGCGCGACTGCGAG CGGGCCGAGTTCCGCATCGAGAGCGAGCCCCCGCAGCCCAACCTCTACAAGTACAACGGCGCCATACGGTGGGAG CAGCCCGTGCCCGGCTACGCCGACGACGACCCCGAGGAGATGACGGAGCCCATCACCATCGACAACCTCCTGCTC CGCGGCTGCAACCTGAGGAACACGGAGTGGGTGCTGGGCGTCGTCATCTTCACCGGCCACGAGACCAAGATCATG ATGAACGCCGGCATCACGCCCAGCAAGCGCGCCAGGATCGCCCGCGAGATGAACTTCAACGTCATCTGCAACTTT GGCATCCTCCTTATCATGTGCCTGCTCTCGGCCATCGTCAACGGCGTCGCCTGGGCGAGGACCGACGCCTCGCTG CACTTCTTCGAGTTCGGCGCCATTGGCGGCAGCGCGCCCGTGAGCGGCTTCATCACCTTCTGGGCCGCCATCATC GTCTTCCAGAACCTGGTGCCCATCTCCCTCTACATCACGCTCGAGATCGTCCGCACGCTCCAGGCCATCTTCATC TTCAGCGACGTCGAGATGTACTACGAGAAGATCGACCAGCCGTGCATCCCCAAGTCGTGGAACATCTCCGACGAC GTCGGCCAGATCGAGTACATCTTCTCCGACAAGACCGGCACCCTCACGCAAAACGTCATGGAGTTCAAGAAGGCC ACCATCAACGGCCAGCCGTACGGCGAGGCCTTCACGGAGGCCCAGGCCGGGATGCAGAAGAGGATGGGCGTCGAC ATCGAGACCGAGGGCGCCAGGATCCGCGCCGAGATTGCCGAGGCCAAGGTCCGGGCCCTGGGCGGCCTGCGCAAG ATCAACAAGAACCCCTACCTCCACGACGACGACGTCACCTTCATCGCCCCGGACTTCGTCTCCGACCTCGCCGGC GACTCCGGGCCCGAGCAGAAGGCGGCCAACGCCGAGTTCATGCTGGCGTTGGCGCTGTGCCACACCGTCATCGCC GAGAGGACGCCCGGCGATCCTCCCAAGATGAATTTCAAGGCGCAGTCGCCCGACGAGGAAGCCCTCGTCGCCACG GCCCGGGACATGGGCTTCACCGTCCTGGGCAATTCCGGCGACGGCATCAACCTCAACGTCATGGGCGAGGAGCGC CACTACCAGATCCTCAACACCATCGAGTTCAACTCGAGCCGGAAGCGGATGAGCTCCATCGTCCGGATGCCAAAC GGCCAGATCGTCCTCTACTGCAAGGGTGCCGACTCCGTCATCTACGCGCGACTGAAGAGGGGCGAGCAGCAGCAG CTCAGGCGGGAGACGGCCGAGCATCTCGAGATGTTCGCCCGGGAAGGCCTGCGGACGCTCTGCATCGCGAGCAAG GTCTTGACGGAGCGCGAGTACAAGGTGTGGAAGAAGGAGCACGACGCTGCCGCCGCGGCGCTCGAGCACCGCGAG GAGAAGCTGGAGGAGGTGGCGGAGCTCATCGAGCAGGACCTGCTGCTGCTGGGCGGAACGGCCATCGAGGATCGG CTGCAAGACGGCGTGCCCGACACCATTGCCCTACTGGGCCAGGCCGGCATCAAGCTCTGGGTCCTGACGGGTGAC AAGGTCGAGACGGCCATCAACATCGGCTTCTCCTGCAACCTGCTCAACAACGACATGGAGCTGATCCACCTCAAG GTCGACGAGGACGAGTCGGGCGAGACCAGCGACGACAGCTTCCTCGAGACGGTCGGCAAGCTGCTCGACCAACAC CTGGCGACGTTCGGAATCGCCGGCAACGACGAAGACCTCGCCCTGGCCAAGAAGAACCACGAACCGCCGGCGCCC ACGCACGGCCTCGTCATCGACGGCTTCACCCTCCGCTGGGCCCTGCACGACGCCCTGAAGCAAAAGTTCCTCCTG CTGTGCAAGCAGTGCAAGTCCGTGCTGTGCTGCCGCGTGAGCCCCGCGCAGAAGGCGGCCGTCGTGGCCATGGTC AAGAACGGCCTGGACGTCATGACCCTGTCCATCGGCGACGGGGCCAACGACGTGGCCATGATCCAGGAGGCCGAT GTTGGCGTGGGCATTGCCGGCGTCGAGGGCCGCCAGGCCGCTATGTCGTCGGACTATGCCATCGCTCAGTTCCGC TTCCTGCAGAGGCTGGTGCTGGTGCACGGCCGCTGGTCCTACCGCCGTCTGGCCGAGAGCATCAGCAACTTCTTC TACAAGAACATGGTCTGGACCTTTAGCATCTTCTGGTTCGAGATCTTCTGCGACTTCGACATCACCTACCTCTTC GACTACACCTACATCCTTATGTTCAACCTCTTCTTCACCTCGCTGCCCGTCGGCATCATGGGCGTGCTCGACCAG GACGTCTCGGACAAGGTTTCGCTCGCCGTTCCCGAGCTGTACCGACGGGGCATCGAGCGGCTCGAGTGGACCCAG CGCAAGTTCTGGCTGTACATGATTGACGGCGTCTACCAATCCGTCATGGTCTTCTTCATCCCCTACCTGCTCTTC ATCCACGGCCGGTCCGTGTCGTTTTCCGGACTGGGCCTCGAGGACAGGCTGCGCTTCGGCGCCTACGTCGCGCAT CCCGCCGTGCTGACCATCAACGGGTACATCCTGATCAACACGTACCGCTGGGACTGGCTGATGGTCCTCATCGTC GTCATCAGCGACCTGTTCATCTTCTTCTGGACCGGCGTCTACACCTCCTTCACCGGGTCCGACTTCTTCTACAAG GCGGCCGCCCAGGTGTACGGCGAGGCCAGCTTCTGGGCCATCTTCTTCATCGTGCCCATCATCTGCCTGTTCCCG CGGTTCGCCATCAAATCGCTGCAGAAGGTGTACTGGCCGTACGACGTCGACATCATCCGAGAGCAGGAGAAGATG GGCCAGTTCGCCTACCTCAATGCCGCAGCCGGGCCGGAGGAGATCAAGGTGAAGAGCAACGACGAGAAGAGCCAG AAGTCGTCGGAAAGCGCCAACAAGACCCAGCACGTGGCCTACGGCAGCGTGGACGAGGACCTGCGTCCCATCTAC CCGCCGTCGACGGCGACGCGGACGACGCACAACCACACGCAGCACGGCAGCGACTCGACCAACTACACGGCCAAC CGCATGTCGATCGAGGTGGCGCCGGTCAACCGCCTGTCGTCGGACGCGCCGGCACACACGCGGCCGTCGATCGAT AGGGCCAGGCCGTCGATCGACAGGGCCAGGCCGTCGTACGACCGGATGCGCATGTCCATGGACCGCTGCCGGCCC AGCTACGAGGCCAGCAGCGACTTCACGACGGCGGCACGGCTGACGCGCATCGAGTCCAGCCAAACGGGCGCCGCC CAAGGGATCAAGGCAAGGCTACGAGGCCTGTCGTTGAGCAAGAATGCCAACAACCAGTCGTAA |
| Gene | >Hirsu2|6991 ATGTCCTCCCCCCCCCGCGCGCCACTCGAGCCCGGCCCCGACCAGAAGATCGAGCACACGCAGAGGGCACGCTGG GCCACCCGCAAGCTGACCGTCAGGAGCGGCCGCATCAAGCGCCTGTCGCTCCTCAACCGCGGCCAGCACCGGCGC GCCGGCTCCAACGAGAAGGACTCGGGCCAAGGCGACCCCAACGAACCGCCCTTGGCCGACCTCCCCGACGGCGGC GAGAGCCATGACATCGTGTCCGACTCGGGCGATTCGCAAGACGACAGCACCAACCGCACCCTCTACTTCAACCTC CCCCTGCCCGACGACTTGCTCGAAGACGGCCACCCCATATACTCCTTTCCTCGGAACAAGATCAGGACAGCAAAG TACACGCCGCTCTCCTTCGTCCCCAAGAACCTGTGGTTCCAGTTCCACAATGTCGCCAACATCTTCTTCCTCTTT CTCGTCATTCTTGTCGTGAGTAGCCCCGCCCCTCCCTTGGCTTTGCCCCCCCTTTCTCCCCCCTCCCCTTGGCGG GCGAGCCACCGGCCGCGCGATGGAGGGAACGCCCCGAACGTTAAGCCACGCCCGCCTCGCAGATATTCCCCATCT TCGGCGGCGTCAACCCCGGGCTCAATGCCGTCCCCCTCATCTTCATCATCGTCGTCACCGCCATCAAAGACGCCA TCGAGGACTACCGCCGAACCATACTCGACATCGAGCTCAACAACGCTCCCGTGCACCGCCTGCACCACTGGAACA ATGTCAACGTCGAGGAGGACAACGTGTCTTCGTGGAGGAGGTTCAAGAAGGCAAACTCCACCTTCTTCGGCTCCA TCTGGCGCGCCATCGAGAGCCTGTGGTCCAAGAAGGCCCGGACGGCTCGCGCCGAGCGCAAGGAACGCAAGCTGA ACCCGCCCGGCGAAGAAGAGGGCCGACCCTCGGTAGAGACGGTGCGCACCAGGCGCTCGATGCGAGAGGCGCTCG CCTCGCCCTTCAACCGCGACTCCTTCATGTCGGCCAATGACGAGATCCGCGAAGAGATCCAGATGACGCCCGTGC CGTCGCCCACCCCGCCCAACAACGCGCCTCGCATCGTGCTGCCCGACGACAGTCAGGACGTTAAGCGCGCCGCCG CCGTGCAGTCGATGAAGTCGGATCTCATCAACTACCAACGTGGTCCCCAGGGGGCCCGCTTCAAAAAGGACGCCT GGAAGAGCCTGCAGGTGGGCGACTTCGTCCGAATCTACAACGACGACGAGCTGCCCGCAGACGTCATCATCCTCT CCACCTCGGACCCCGACGGCGCCTGTTACGTCGAGACGAAGAACCTGGACGGCGAGACGAACCTCAAGGTTCGCC AGGCCCTGCGCTGCGGCCGATCCCTCAAGCACGCGCGCGACTGCGAGCGGGCCGAGTTCCGCATCGAGAGCGAGC CCCCGCAGCCCAACCTCTACAAGTACAACGGCGCCATACGGTGGGAGCAGCCCGTGCCCGGCTACGCCGACGACG ACCCCGAGGAGATGACGGAGCCCATCACCATCGACAACCTCCTGCTCCGCGGCTGCAACCTGAGGAACACGGAGT GGGTGCTGGGCGTCGTCATCTTCACCGGCCACGAGACCAAGATCATGATGAACGCCGGCATCACGCCCAGCAAGC GCGCCAGGATCGCCCGCGAGATGAACTTCAACGTCATCTGCAACTTTGGCATCCTCCTTATCATGTGCCTGCTCT CGGCCATCGTCAACGGCGTCGCCTGGGCGAGGACCGACGCCTCGCTGCACTTCTTCGAGTTCGGCGCCATTGGCG GCAGCGCGCCCGTGAGCGGCTTCATCACCTTCTGGGCCGCCATCATCGTCTTCCAGAACCTGGTGCCCATCTCCC TCTACATCACGCTCGAGATCGTCCGCACGCTCCAGGCCATCTTCATCTTCAGCGACGTCGAGATGTACTACGAGA AGATCGACCAGCCGTGCATCCCCAAGTCGTGGAACATCTCCGACGACGTCGGCCAGATCGAGTACATCTTCTCCG ACAAGACCGGCACCCTCACGCAAAACGTCATGGAGTTCAAGAAGGCCACCATCAACGGCCAGCCGTACGGCGAGG CCTTCACGGAGGCCCAGGCCGGGATGCAGAAGAGGATGGGCGTCGACATCGAGACCGAGGGCGCCAGGATCCGCG CCGAGATTGCCGAGGCCAAGGTCCGGGCCCTGGGCGGCCTGCGCAAGATCAACAAGAACCCCTACCTCCACGACG ACGACGTCACCTTCATCGCCCCGGACTTCGTCTCCGACCTCGCCGGCGACTCCGGGCCCGAGCAGAAGGCGGCCA ACGCCGAGTTCATGCTGGCGTTGGCGCTGTGCCACACCGTCATCGCCGAGAGGACGCCCGGCGATCCTCCCAAGA TGAATTTCAAGGCGCAGTCGCCCGACGAGGAAGCCCTCGTCGCCACGGCCCGGGACATGGGCTTCACCGTCCTGG GCAATTCCGGCGACGGCATCAACCTCAACGTCATGGGCGAGGAGCGCCACTACCAGATCCTCAACACCATCGAGT TCAACTCGAGCCGGAAGCGGATGAGCTCCATCGTCCGGATGCCAAACGGCCAGATCGTCCTCTACTGCAAGGGTG CCGACTCCGTCATCTACGCGCGACTGAAGAGGGGCGAGCAGCAGCAGCTCAGGCGGGAGACGGCCGAGCATCTCG AGATGTTCGCCCGGGAAGGCCTGCGGACGCTCTGCATCGCGAGCAAGGTCTTGACGGAGCGCGAGTACAAGGTGT GGAAGAAGGAGCACGACGCTGCCGCCGCGGCGCTCGAGCACCGCGAGGAGAAGCTGGAGGAGGTGGCGGAGCTCA TCGAGCAGGACCTGCTGCTGCTGGGCGGAACGGCCATCGAGGATCGGCTGCAAGACGGCGTGCCCGACACCATTG CCCTACTGGGCCAGGCCGGCATCAAGCTCTGGGTCCTGACGGGTGACAAGGTCGAGACGGCCATCAACATCGGCT TCTCCTGCAACCTGCTCAACAACGACATGGAGCTGATCCACCTCAAGGTCGACGAGGACGAGTCGGGCGAGACCA GCGACGACAGCTTCCTCGAGACGGTCGGCAAGCTGCTCGACCAACACCTGGCGACGTTCGGAATCGCCGGCAACG ACGAAGACCTCGCCCTGGCCAAGAAGAACCACGAACCGCCGGCGCCCACGCACGGCCTCGTCATCGACGGCTTCA CCCTCCGCTGGGCCCTGCACGACGCCCTGAAGCAAAAGTTCCTCCTGCTGTGCAAGCAGTGCAAGTCCGTGCTGT GCTGCCGCGTGAGCCCCGCGCAGAAGGCGGCCGTCGTGGCCATGGTCAAGAACGGCCTGGACGTCATGACCCTGT CCATCGGCGACGGGGCCAACGACGTGGCCATGATCCAGGAGGCCGATGTTGGCGTGGGCATTGCCGGCGTCGAGG GCCGCCAGGCCGCTATGTCGTCGGACTATGCCATCGCTCAGTTCCGCTTCCTGCAGAGGCTGGTGCTGGTGCACG GCCGCTGGTCCTACCGCCGTCTGGCCGAGAGCATCAGCAACTTCTTCTACAAGAACATGGTCTGGACCTTTAGCA TCTTCTGGTTCGAGATCTTCTGCGACTTCGACATCACCTACCTCTTCGACTACACCTACATCCTTATGTTCAACC TCTTCTTCACCTCGCTGCCCGTCGGCATCATGGGCGTGCTCGACCAGGACGTCTCGGACAAGGTTTCGCTCGCCG TTCCCGAGCTGTACCGACGGGGCATCGAGCGGCTCGAGTGGACCCAGCGCAAGTTCTGGTAAGTCACAGGTTTTT TTTTTTTTTGCTGCCCATGCCGCGCGCGCACCGCGGATGCGTGTCTGTGGACCGATTGCTGACGAGAGCCTCGCC GATCCGCAGGCTGTACATGATTGACGGCGTCTACCAATCCGTCATGGTCTTCTTCATCCCCTACCTGCTCTTCAT CCACGGCCGGTCCGTGTCGTTTTCCGGACTGGGCCTCGAGGACAGGCTGCGCTTCGGCGCCTACGTCGCGCATCC CGCCGTGCTGACCATCAACGGGTACATCCTGATCAACACGTACCGCTGGGACTGGCTGATGGTCCTCATCGTCGT CATCAGCGACCTGTTCATCTTCTTCTGGACCGGCGTCTACACCTCCTTCACCGGGTCCGACTTCTTCTACAAGGC GGCCGCCCAGGTGTACGGCGAGGCCAGCTTCTGGGCCATCTTCTTCATCGTGCCCATCATCTGCCTGTTCCCGCG GTTCGCCATCAAATCGCTGCAGAAGGTGTACTGGCCGTACGACGTCGACATCATCCGAGAGCAGGAGAAGATGGG CCAGTTCGCCTACCTCAATGCCGCAGCCGGGCCGGAGGAGATCAAGGTGAAGAGCAACGACGAGAAGAGCCAGAA GTCGTCGGAAAGCGCCAACAAGACCCAGCACGTGGCCTACGGCAGCGTGGACGAGGACCTGCGTCCCATCTACCC GCCGTCGACGGCGACGCGGACGACGCACAACCACACGCAGCACGGCAGCGACTCGACCAACTACACGGCCAACCG CATGTCGATCGAGGTGGCGCCGGTCAACCGCCTGTCGTCGGACGCGCCGGCACACACGCGGCCGTCGATCGATAG GGCCAGGCCGTCGATCGACAGGGCCAGGCCGTCGTACGACCGGATGCGCATGTCCATGGACCGCTGCCGGCCCAG CTACGAGGCCAGCAGCGACTTCACGACGGCGGCACGGCTGACGCGCATCGAGTCCAGCCAAACGGGCGCCGCCCA AGGGATCAAGGCAAGGCTACGAGGCCTGTCGTTGAGCAAGAATGCCAACAACCAGTCGTAA |