Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|5222
Gene name
Locationscaffold_420:14661..18470
Strand+
Gene length (bp)3809
Transcript length (bp)3753
Coding sequence length (bp)3750
Protein length (aa) 1250

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF16212 PhoLip_ATPase_C Phospholipid-translocating P-type ATPase C-terminal 1.4E-57 1082 1249
PF16209 PhoLip_ATPase_N Phospholipid-translocating ATPase N-terminal 1.3E-21 84 140
PF00702 Hydrolase haloacid dehalogenase-like hydrolase 1.1E-07 480 990
PF13246 Cation_ATPase Cation transport ATPase (P-type) 1.0E-09 625 708
PF00122 E1-E2_ATPase E1-E2 ATPase 1.5E-09 226 435

Swissprot hits

[Show all]
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 49 1248 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 7 1250 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 53 709 6.0E-97
sp|Q9Y2Q0|AT8A1_HUMAN Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 87 709 4.0E-92
sp|P70704|AT8A1_MOUSE Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 87 709 1.0E-91
[Show all]
[Show less]
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 49 1248 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 7 1250 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 53 709 6.0E-97
sp|Q9Y2Q0|AT8A1_HUMAN Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 87 709 4.0E-92
sp|P70704|AT8A1_MOUSE Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 87 709 1.0E-91
sp|Q9LVK9|ALA7_ARATH Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 87 709 4.0E-91
sp|C7EXK4|AT8A2_BOVIN Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 85 718 4.0E-90
sp|Q9NTI2|AT8A2_HUMAN Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 85 718 2.0E-89
sp|Q9SLK6|ALA6_ARATH Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 87 712 2.0E-89
sp|Q9SX33|ALA9_ARATH Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 41 709 5.0E-89
sp|P98200|AT8A2_MOUSE Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 85 718 2.0E-88
sp|Q9LK90|ALA8_ARATH Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 87 709 3.0E-88
sp|Q9LNQ4|ALA4_ARATH Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 75 709 5.0E-88
sp|Q9SGG3|ALA5_ARATH Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 75 709 6.0E-88
sp|O94296|YOOC_SCHPO Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 15 709 8.0E-88
sp|P57792|ALA12_ARATH Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 87 709 2.0E-87
sp|Q9U280|TAT1_CAEEL Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 775 1250 1.0E-86
sp|Q9LI83|ALA10_ARATH Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 87 709 3.0E-86
sp|Q9XIE6|ALA3_ARATH Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 87 709 4.0E-86
sp|Q9SAF5|ALA11_ARATH Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 87 709 2.0E-85
sp|P70704|AT8A1_MOUSE Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 843 1243 9.0E-85
sp|Q29449|AT8A1_BOVIN Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 843 1243 1.0E-84
sp|Q9Y2Q0|AT8A1_HUMAN Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 843 1243 3.0E-84
sp|Q9NTI2|AT8A2_HUMAN Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 773 1212 5.0E-84
sp|C7EXK4|AT8A2_BOVIN Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 773 1212 2.0E-83
sp|Q5BL50|AT8B1_XENTR Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 73 709 8.0E-83
sp|P39524|ATC3_YEAST Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 844 1213 9.0E-83
sp|Q9LNQ4|ALA4_ARATH Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 844 1244 3.0E-82
sp|Q9SGG3|ALA5_ARATH Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 844 1244 3.0E-82
sp|P98200|AT8A2_MOUSE Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 773 1212 4.0E-82
sp|O94296|YOOC_SCHPO Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 845 1200 8.0E-82
sp|P98198|AT8B2_HUMAN Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 87 713 4.0E-80
sp|P98199|AT8B2_MOUSE Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 87 709 2.0E-79
sp|Q9LVK9|ALA7_ARATH Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 844 1244 4.0E-79
sp|Q9GKS6|AT10D_MACFA Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 844 1187 9.0E-79
sp|Q6UQ17|AT8B3_MOUSE Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 83 710 1.0E-78
sp|O94823|AT10B_HUMAN Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 824 1245 7.0E-78
sp|Q9P241|AT10D_HUMAN Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 844 1235 8.0E-78
sp|Q9XIE6|ALA3_ARATH Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 845 1250 9.0E-78
sp|Q9SLK6|ALA6_ARATH Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 844 1244 2.0E-77
sp|Q8K2X1|AT10D_MOUSE Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 841 1187 2.0E-77
sp|O36028|ATCZ_SCHPO Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 89 709 8.0E-77
sp|P98204|ALA1_ARATH Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 81 703 2.0E-76
sp|Q8TF62|AT8B4_HUMAN Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 87 709 2.0E-76
sp|A3FIN4|AT8B5_MOUSE Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 87 716 2.0E-76
sp|O60423|AT8B3_HUMAN Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 87 709 2.0E-75
sp|Q9LK90|ALA8_ARATH Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 844 1212 1.0E-74
sp|Q9LI83|ALA10_ARATH Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 844 1249 1.0E-74
sp|O54827|AT10A_MOUSE Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 845 1247 1.0E-74
sp|P98198|AT8B2_HUMAN Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 827 1242 2.0E-74
sp|O36028|ATCZ_SCHPO Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 835 1250 3.0E-73
sp|Q8TF62|AT8B4_HUMAN Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 845 1240 3.0E-73
sp|P32660|ATC5_YEAST Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 845 1250 4.0E-73
sp|P57792|ALA12_ARATH Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 845 1212 1.0E-72
sp|Q9SAF5|ALA11_ARATH Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 845 1245 1.0E-72
sp|O60312|AT10A_HUMAN Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 845 1247 2.0E-72
sp|Q12675|ATC4_YEAST Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 833 1218 3.0E-72
sp|P98199|AT8B2_MOUSE Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 824 1242 6.0E-72
sp|Q9SX33|ALA9_ARATH Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 845 1200 3.0E-71
sp|Q5BL50|AT8B1_XENTR Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 773 1218 3.0E-71
sp|P32660|ATC5_YEAST Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 87 709 3.0E-71
sp|A3FIN4|AT8B5_MOUSE Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 845 1229 6.0E-70
sp|Q9Y2G3|AT11B_HUMAN Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 87 720 6.0E-70
sp|P98204|ALA1_ARATH Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 845 1212 1.0E-69
sp|Q9N0Z4|AT11B_RABIT Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 87 720 3.0E-69
sp|Q09891|ATCX_SCHPO Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 845 1212 5.0E-69
sp|Q148W0|AT8B1_MOUSE Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 846 1197 7.0E-69
sp|O43520|AT8B1_HUMAN Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 846 1197 2.0E-68
sp|P98205|ALA2_ARATH Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 846 1246 7.0E-68
sp|P98196|AT11A_HUMAN Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 87 727 1.0E-67
sp|Q9Y2G3|AT11B_HUMAN Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 819 1249 8.0E-67
sp|Q148W0|AT8B1_MOUSE Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 74 513 8.0E-66
sp|Q9P241|AT10D_HUMAN Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 24 507 2.0E-65
sp|Q8K2X1|AT10D_MOUSE Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 65 564 4.0E-65
sp|Q29449|AT8A1_BOVIN Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 87 505 3.0E-64
sp|O43520|AT8B1_HUMAN Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 74 513 4.0E-64
sp|Q09891|ATCX_SCHPO Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 225 709 2.0E-63
sp|P98196|AT11A_HUMAN Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 850 1249 3.0E-63
sp|O94823|AT10B_HUMAN Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 87 526 1.0E-62
sp|Q9N0Z4|AT11B_RABIT Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 819 1249 1.0E-61
sp|Q12675|ATC4_YEAST Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 201 709 5.0E-61
sp|Q9QZW0|AT11C_MOUSE Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 845 1249 5.0E-61
sp|O54827|AT10A_MOUSE Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 90 507 6.0E-61
sp|P98197|AT11A_MOUSE Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 850 1249 8.0E-61
sp|Q8NB49|AT11C_HUMAN Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 845 1249 2.0E-60
sp|Q9U280|TAT1_CAEEL Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 60 541 7.0E-60
sp|O60312|AT10A_HUMAN Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 82 507 9.0E-59
sp|O43861|ATP9B_HUMAN Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 790 1213 6.0E-57
sp|F1Q4S1|ATP9B_DANRE Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 848 1213 1.0E-56
sp|A1A4J6|ATP9B_BOVIN Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 790 1213 3.0E-56
sp|P98195|ATP9B_MOUSE Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 790 1213 3.0E-56
sp|D4ABB8|ATP9B_RAT Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 790 1213 1.0E-55
sp|O60423|AT8B3_HUMAN Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 846 1228 2.0E-55
sp|O70228|ATP9A_MOUSE Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 848 1213 2.0E-55
sp|O75110|ATP9A_HUMAN Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 848 1213 2.0E-55
sp|P98197|AT11A_MOUSE Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 87 506 9.0E-55
sp|Q8NB49|AT11C_HUMAN Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 87 518 9.0E-55
sp|Q9QZW0|AT11C_MOUSE Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 72 518 6.0E-54
sp|P40527|ATC7_YEAST Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 848 1207 5.0E-50
sp|Q10309|YD56_SCHPO Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 848 1210 7.0E-49
sp|P40527|ATC7_YEAST Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 62 705 2.0E-47
sp|O70228|ATP9A_MOUSE Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 82 705 7.0E-47
sp|O75110|ATP9A_HUMAN Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 82 705 2.0E-46
sp|P98195|ATP9B_MOUSE Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 49 750 7.0E-46
sp|D4ABB8|ATP9B_RAT Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 49 750 8.0E-46
sp|P98205|ALA2_ARATH Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 90 505 2.0E-45
sp|F1Q4S1|ATP9B_DANRE Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 38 702 4.0E-45
sp|O43861|ATP9B_HUMAN Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 38 707 9.0E-45
sp|A1A4J6|ATP9B_BOVIN Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 49 702 1.0E-44
sp|Q6UQ17|AT8B3_MOUSE Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 996 1198 3.0E-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 87 529 4.0E-38
sp|Q29449|AT8A1_BOVIN Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 601 709 8.0E-22
sp|Q6UQ17|AT8B3_MOUSE Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 846 951 1.0E-19
sp|O43520|AT8B1_HUMAN Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 600 709 1.0E-19
sp|Q148W0|AT8B1_MOUSE Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 600 781 3.0E-19
sp|Q9U280|TAT1_CAEEL Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 547 748 1.0E-15
sp|Q10309|YD56_SCHPO Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 591 705 9.0E-14
sp|Q9QZW0|AT11C_MOUSE Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 591 732 2.0E-12
sp|Q8NB49|AT11C_HUMAN Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 602 732 2.0E-11
sp|P98205|ALA2_ARATH Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 602 760 8.0E-10
sp|P98197|AT11A_MOUSE Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 602 743 9.0E-10
sp|O94823|AT10B_HUMAN Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 614 710 2.0E-09
sp|Q3TYU2|AT135_MOUSE Probable cation-transporting ATPase 13A5 OS=Mus musculus GN=Atp13a5 PE=2 SV=2 889 1078 3.0E-09
sp|Q9GKS6|AT10D_MACFA Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 623 713 2.0E-08
sp|Q09891|ATCX_SCHPO Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 90 165 5.0E-08
sp|Q9P241|AT10D_HUMAN Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 527 713 1.0E-07
sp|Q8K2X1|AT10D_MOUSE Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 614 712 1.0E-07
sp|O54827|AT10A_MOUSE Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 615 709 1.0E-07
sp|P35317|AT1A_HYDVU Sodium/potassium-transporting ATPase subunit alpha OS=Hydra vulgaris PE=2 SV=1 830 1077 3.0E-07
sp|Q5XF90|AT134_MOUSE Probable cation-transporting ATPase 13A4 OS=Mus musculus GN=Atp13a4 PE=2 SV=1 845 1078 6.0E-07
sp|Q9WV27|AT1A4_MOUSE Sodium/potassium-transporting ATPase subunit alpha-4 OS=Mus musculus GN=Atp1a4 PE=1 SV=3 900 1077 1.0E-06
sp|Q4VNC1|AT134_HUMAN Probable cation-transporting ATPase 13A4 OS=Homo sapiens GN=ATP13A4 PE=2 SV=3 845 1078 2.0E-06
sp|Q5ZKB7|AT134_CHICK Probable cation-transporting ATPase 13A4 OS=Gallus gallus GN=ATP13A4 PE=2 SV=1 879 1078 2.0E-06
sp|P19156|ATP4A_PIG Potassium-transporting ATPase alpha chain 1 OS=Sus scrofa GN=ATP4A PE=1 SV=3 853 1160 2.0E-06
sp|O60312|AT10A_HUMAN Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 621 724 3.0E-06
sp|P50996|ATP4A_CANLF Potassium-transporting ATPase alpha chain 1 OS=Canis lupus familiaris GN=ATP4A PE=2 SV=3 853 1160 5.0E-06
sp|Q92036|AT12A_RHIMB Potassium-transporting ATPase alpha chain 2 OS=Rhinella marina GN=ATP12A PE=2 SV=1 899 1131 7.0E-06
sp|P09626|ATP4A_RAT Potassium-transporting ATPase alpha chain 1 OS=Rattus norvegicus GN=Atp4a PE=1 SV=3 853 1160 7.0E-06
sp|Q64436|ATP4A_MOUSE Potassium-transporting ATPase alpha chain 1 OS=Mus musculus GN=Atp4a PE=1 SV=3 853 1160 9.0E-06
sp|O53114|CTPI_MYCLE Probable cation-transporting ATPase I OS=Mycobacterium leprae (strain TN) GN=ctpI PE=3 SV=1 901 1168 9.0E-06
[Show less]

GO

(None)

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 34 0.45

Transmembrane Domains

Domain # Start End Length
1 374 396 22
2 417 439 22
3 1199 1221 22
4 1228 1247 19

Transcription Factor Class

(None)

Expression data

Analysis 1: Expression analysis during behavioral modification. Published in De Bekker et al., 2017.

Click here for more information

Sequences

Type of sequenceSequence
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 >Ophio5|5222
MSSASLPEKAPAFLVSSPHRPFDDDDPGPRLPLRNRFWAALQSLYQATIVHLILRKKHIDATKHGRHIPLAIDHQ
KPLIDTRRGHAYLSNDVRTSRYTIWDFIPKQFFFQFSRVGNFYFLCVGIPQTIPGLSTTGSFTTILPLLFFVLLT
VAKEGYDDYRRHLLDKVENANFVTVLGRHDLSVVHARSSRSWRRWVSFRTESTSQPRPSLPKDEYLGVRWVPSRW
SHVKVGDVVLLSRDEPVPADLVLLHSDGENGIAYIDTMALDGETSLKTKQVCHALHGCGSIQGIAECRAEFVVED
PNPDLFNFNGRVTVRDKTVPLTLSHVVYRGSVVRNTTRAIGLVVNTGEECKVRMNSNQHPRAKRPALEKIVNKVV
LTLAIYVLVLSVGVSMGYVHFRADYEKHAWFLDGATVPFHQIIIAFVIMFNNIVPLSLYISLEIVKVGQLLLLNS
DVEMYDEETDTPARCNTNTIMENLGQIGYVFSDKTGTLTDNVMRFRKLSVAGTVWLHAMDLEQPETDGPPTPSSL
DRHSVRKPTVSKASAIPEDERKTPTLASRSSLGRRPSSQWRSTGRPDLVQPEVNTSDLLEHMRLRPHSAFSRTAR
DYLLAVAICHTCLPEVKNGRIEFQASSPDELALVRAAQELGFGVTHRTSQSITLQVSRPSGQSEKMVFQILDVIE
FSSTRKRMSIVVRYPDGRTSIVCKGADSVILPRLRLSTLAMQRAHEVRKSADLEREMQRRSEQQEPRNSFGGRRS
LTVWRNAEVATDASGGRRSLASRSRSFEVNKMTRSSVDRPRTSVLARRGVSLDVSRNQSTSSTAAHLRPQHDRLD
FLNDPAMHDESEVFNRCFRHLDDFATEGLRTLVYAQRFISDSEYRTWKKLYDEATTSLHDRQVMIEAAGELIETS
LELVGATAIEDKLQKGVPETIDRLRRANIKIWMVTGDKRETAINIAHSARICRPGSDLYVLDVDRSLLETQLVAL
AEDLQAGSVHSVVVIDGQTLAAVEKSAELSRRFFSLAMTVDSVICCRASPAQKAILVRAVRARLGTLKDKDRRGL
TLAIGDGANDLAMIQASHVGVGISGKEGLQAARVADYAIAQFRFLQRLLLVHGRWNYVRTAKFILCTFWKEMFFY
LPTAIYQRCSGYSGTSLYQEVSLTVFNTLFTSLCTICMGVWEQDLSAETLLAVPELYVYGQRGLGLNMSKYLRWM
AVAAVQGLAVWYGVWAGYGIVSPSAHDEGLYALGTLAFTVGVLWINWKLL
Coding >Ophio5|5222
ATGTCTTCCGCCTCGTTACCCGAGAAGGCTCCCGCGTTCCTCGTCTCGAGTCCGCATCGTCCCTTCGATGACGAC
GACCCCGGCCCTCGTCTGCCTCTGCGAAACCGCTTCTGGGCCGCCCTACAGTCGCTTTACCAGGCTACCATCGTC
CATCTGATACTGCGCAAGAAGCACATCGACGCCACCAAGCATGGCAGGCACATTCCACTTGCCATTGACCACCAA
AAGCCGCTCATCGACACCCGCCGCGGCCACGCCTATCTTTCCAACGATGTCCGCACCTCTCGCTATACCATATGG
GACTTTATACCCAAGCAATTCTTCTTTCAGTTTTCCCGTGTCGGAAACTTTTACTTCCTCTGCGTCGGCATCCCC
CAGACGATACCGGGCCTGTCCACGACGGGCTCCTTTACCACCATTTTACCTTTATTGTTCTTCGTCCTCCTCACC
GTGGCCAAGGAGGGCTATGATGACTACAGACGGCATCTCTTGGACAAGGTTGAGAATGCAAACTTCGTCACTGTC
CTCGGCCGCCATGACCTGAGTGTCGTCCATGCCAGGTCGTCTCGTTCTTGGCGCCGCTGGGTCTCCTTTCGCACC
GAATCCACCAGCCAGCCAAGGCCGTCGCTCCCCAAAGATGAGTACCTCGGCGTTCGATGGGTGCCCTCTCGATGG
AGTCACGTCAAGGTTGGAGACGTCGTCTTGCTGTCCCGCGACGAACCGGTCCCCGCCGACTTGGTCCTTCTTCAT
AGTGATGGCGAGAACGGCATTGCCTACATCGACACCATGGCCTTGGACGGCGAAACCAGTCTCAAGACGAAGCAG
GTTTGCCACGCCCTTCACGGATGTGGCTCTATCCAGGGCATTGCCGAATGCCGGGCCGAGTTCGTCGTCGAGGAC
CCGAATCCAGACCTTTTCAACTTCAATGGCCGCGTCACCGTCCGGGACAAAACCGTGCCCCTGACCCTCAGCCAT
GTCGTCTACCGGGGCAGCGTTGTGCGGAACACGACCCGCGCCATCGGTCTCGTTGTCAACACGGGTGAGGAGTGC
AAGGTCCGCATGAACTCCAACCAACACCCGCGTGCGAAGCGGCCGGCCCTCGAGAAGATCGTCAACAAGGTCGTC
CTGACCCTGGCAATTTACGTCCTTGTCCTCTCCGTCGGCGTCTCCATGGGCTATGTTCACTTTCGTGCCGACTAC
GAGAAGCATGCCTGGTTCCTCGACGGCGCCACAGTCCCGTTTCACCAGATCATCATCGCCTTCGTCATCATGTTC
AACAACATTGTACCCCTATCCTTGTATATATCACTGGAAATTGTCAAGGTCGGCCAGCTTCTTCTACTCAACTCT
GACGTCGAAATGTACGACGAGGAGACGGACACGCCGGCGCGATGTAATACCAACACCATCATGGAAAACCTCGGC
CAAATTGGCTACGTCTTCTCCGACAAGACGGGAACTCTGACGGACAACGTCATGAGGTTCCGCAAGCTCAGCGTC
GCCGGCACCGTCTGGCTTCACGCCATGGACCTCGAGCAGCCCGAGACCGACGGGCCTCCGACGCCCTCTTCGCTC
GACCGGCATTCGGTTCGGAAGCCGACGGTGAGCAAGGCCTCGGCCATCCCCGAGGACGAACGCAAAACCCCGACG
TTGGCATCGCGGTCATCGCTGGGCCGGAGGCCATCGTCACAATGGCGTTCCACCGGTCGCCCAGACCTCGTACAG
CCCGAGGTCAACACGTCAGATCTCCTGGAGCACATGAGGCTCCGGCCGCATTCCGCCTTCTCCAGGACAGCCAGA
GACTATTTGCTCGCCGTCGCCATCTGCCACACTTGCCTGCCCGAAGTCAAGAACGGAAGGATCGAGTTCCAGGCG
TCTTCGCCCGATGAGCTGGCTCTAGTGAGAGCAGCTCAGGAGCTTGGCTTTGGCGTGACCCATCGCACGTCGCAA
AGCATAACACTGCAGGTTTCGCGGCCCAGCGGCCAGAGCGAGAAGATGGTTTTCCAGATTCTGGACGTCATCGAG
TTTAGCAGCACGCGCAAGAGAATGTCCATTGTCGTTCGCTATCCCGATGGGCGCACATCCATCGTATGCAAAGGC
GCCGACTCGGTCATTCTGCCTAGGCTCAGGCTGTCCACTCTGGCGATGCAGAGGGCACACGAGGTCCGGAAGAGT
GCCGACCTCGAGCGCGAGATGCAGCGGCGCAGCGAGCAGCAGGAGCCCCGGAACAGCTTTGGCGGGAGGCGAAGC
CTGACCGTCTGGCGAAACGCCGAAGTCGCGACTGATGCTAGCGGAGGCCGGCGCTCACTGGCCAGCCGCAGCAGA
TCTTTCGAGGTTAACAAGATGACTCGGTCGTCCGTTGACCGACCTCGGACCTCGGTTCTCGCCCGGCGAGGAGTC
TCGCTTGACGTGTCTCGAAACCAGTCCACGAGCTCGACGGCCGCTCACTTGCGGCCCCAGCACGATCGTCTGGAC
TTTCTCAACGATCCTGCCATGCACGATGAGTCCGAGGTTTTCAACCGGTGCTTCAGGCACCTGGATGACTTCGCC
ACAGAAGGTCTCAGGACCCTTGTCTATGCTCAAAGGTTTATCTCGGATTCGGAATACCGCACGTGGAAGAAACTC
TACGACGAGGCGACGACGAGCCTTCACGACCGACAGGTAATGATAGAGGCCGCCGGTGAGCTGATTGAGACAAGT
CTCGAACTCGTCGGCGCCACCGCCATCGAAGACAAGCTGCAAAAGGGCGTCCCGGAGACTATAGACAGACTGCGA
CGGGCCAACATCAAGATCTGGATGGTGACGGGTGATAAGCGTGAGACGGCCATCAATATTGCCCACTCGGCGCGC
ATCTGCCGACCGGGATCCGACCTCTACGTCCTGGATGTGGACAGAAGTCTTCTGGAGACGCAGCTCGTGGCCCTG
GCCGAGGATTTGCAGGCCGGTTCCGTCCACAGCGTCGTCGTCATCGACGGGCAGACGCTGGCCGCGGTGGAGAAG
TCGGCCGAGCTGTCGAGACGCTTCTTCAGCCTGGCCATGACGGTCGACTCCGTAATCTGCTGTCGGGCGTCGCCG
GCGCAGAAGGCGATACTGGTCCGGGCCGTGCGCGCGCGCCTGGGTACCCTAAAAGACAAGGACCGGCGCGGGCTT
ACGCTGGCCATCGGCGACGGCGCAAATGATCTCGCCATGATCCAGGCCAGCCACGTCGGTGTCGGCATATCCGGA
AAGGAGGGCCTCCAGGCGGCGCGCGTGGCCGACTATGCCATCGCCCAGTTCCGCTTCCTACAGCGGCTGCTCCTC
GTCCACGGTCGCTGGAACTACGTGCGGACGGCAAAGTTTATCCTTTGCACCTTTTGGAAGGAGATGTTCTTCTAT
CTGCCGACGGCCATATACCAGAGATGCAGCGGCTACAGCGGCACCTCGTTGTACCAGGAGGTGAGCCTGACCGTC
TTCAACACGCTCTTCACCAGCCTCTGCACCATCTGCATGGGCGTCTGGGAGCAGGACTTGAGCGCCGAGACGCTG
CTGGCCGTGCCCGAGCTGTACGTCTACGGCCAACGCGGCCTGGGGCTCAACATGTCCAAGTATCTGCGCTGGATG
GCCGTGGCCGCTGTCCAAGGTTTGGCCGTCTGGTACGGCGTCTGGGCCGGATACGGCATCGTCTCGCCGTCGGCT
CACGACGAGGGCCTCTACGCGCTGGGGACGCTGGCCTTTACCGTCGGCGTCTTGTGGATCAACTGGAAGCTATTG
Transcript >Ophio5|5222
ATGTCTTCCGCCTCGTTACCCGAGAAGGCTCCCGCGTTCCTCGTCTCGAGTCCGCATCGTCCCTTCGATGACGAC
GACCCCGGCCCTCGTCTGCCTCTGCGAAACCGCTTCTGGGCCGCCCTACAGTCGCTTTACCAGGCTACCATCGTC
CATCTGATACTGCGCAAGAAGCACATCGACGCCACCAAGCATGGCAGGCACATTCCACTTGCCATTGACCACCAA
AAGCCGCTCATCGACACCCGCCGCGGCCACGCCTATCTTTCCAACGATGTCCGCACCTCTCGCTATACCATATGG
GACTTTATACCCAAGCAATTCTTCTTTCAGTTTTCCCGTGTCGGAAACTTTTACTTCCTCTGCGTCGGCATCCCC
CAGACGATACCGGGCCTGTCCACGACGGGCTCCTTTACCACCATTTTACCTTTATTGTTCTTCGTCCTCCTCACC
GTGGCCAAGGAGGGCTATGATGACTACAGACGGCATCTCTTGGACAAGGTTGAGAATGCAAACTTCGTCACTGTC
CTCGGCCGCCATGACCTGAGTGTCGTCCATGCCAGGTCGTCTCGTTCTTGGCGCCGCTGGGTCTCCTTTCGCACC
GAATCCACCAGCCAGCCAAGGCCGTCGCTCCCCAAAGATGAGTACCTCGGCGTTCGATGGGTGCCCTCTCGATGG
AGTCACGTCAAGGTTGGAGACGTCGTCTTGCTGTCCCGCGACGAACCGGTCCCCGCCGACTTGGTCCTTCTTCAT
AGTGATGGCGAGAACGGCATTGCCTACATCGACACCATGGCCTTGGACGGCGAAACCAGTCTCAAGACGAAGCAG
GTTTGCCACGCCCTTCACGGATGTGGCTCTATCCAGGGCATTGCCGAATGCCGGGCCGAGTTCGTCGTCGAGGAC
CCGAATCCAGACCTTTTCAACTTCAATGGCCGCGTCACCGTCCGGGACAAAACCGTGCCCCTGACCCTCAGCCAT
GTCGTCTACCGGGGCAGCGTTGTGCGGAACACGACCCGCGCCATCGGTCTCGTTGTCAACACGGGTGAGGAGTGC
AAGGTCCGCATGAACTCCAACCAACACCCGCGTGCGAAGCGGCCGGCCCTCGAGAAGATCGTCAACAAGGTCGTC
CTGACCCTGGCAATTTACGTCCTTGTCCTCTCCGTCGGCGTCTCCATGGGCTATGTTCACTTTCGTGCCGACTAC
GAGAAGCATGCCTGGTTCCTCGACGGCGCCACAGTCCCGTTTCACCAGATCATCATCGCCTTCGTCATCATGTTC
AACAACATTGTACCCCTATCCTTGTATATATCACTGGAAATTGTCAAGGTCGGCCAGCTTCTTCTACTCAACTCT
GACGTCGAAATGTACGACGAGGAGACGGACACGCCGGCGCGATGTAATACCAACACCATCATGGAAAACCTCGGC
CAAATTGGCTACGTCTTCTCCGACAAGACGGGAACTCTGACGGACAACGTCATGAGGTTCCGCAAGCTCAGCGTC
GCCGGCACCGTCTGGCTTCACGCCATGGACCTCGAGCAGCCCGAGACCGACGGGCCTCCGACGCCCTCTTCGCTC
GACCGGCATTCGGTTCGGAAGCCGACGGTGAGCAAGGCCTCGGCCATCCCCGAGGACGAACGCAAAACCCCGACG
TTGGCATCGCGGTCATCGCTGGGCCGGAGGCCATCGTCACAATGGCGTTCCACCGGTCGCCCAGACCTCGTACAG
CCCGAGGTCAACACGTCAGATCTCCTGGAGCACATGAGGCTCCGGCCGCATTCCGCCTTCTCCAGGACAGCCAGA
GACTATTTGCTCGCCGTCGCCATCTGCCACACTTGCCTGCCCGAAGTCAAGAACGGAAGGATCGAGTTCCAGGCG
TCTTCGCCCGATGAGCTGGCTCTAGTGAGAGCAGCTCAGGAGCTTGGCTTTGGCGTGACCCATCGCACGTCGCAA
AGCATAACACTGCAGGTTTCGCGGCCCAGCGGCCAGAGCGAGAAGATGGTTTTCCAGATTCTGGACGTCATCGAG
TTTAGCAGCACGCGCAAGAGAATGTCCATTGTCGTTCGCTATCCCGATGGGCGCACATCCATCGTATGCAAAGGC
GCCGACTCGGTCATTCTGCCTAGGCTCAGGCTGTCCACTCTGGCGATGCAGAGGGCACACGAGGTCCGGAAGAGT
GCCGACCTCGAGCGCGAGATGCAGCGGCGCAGCGAGCAGCAGGAGCCCCGGAACAGCTTTGGCGGGAGGCGAAGC
CTGACCGTCTGGCGAAACGCCGAAGTCGCGACTGATGCTAGCGGAGGCCGGCGCTCACTGGCCAGCCGCAGCAGA
TCTTTCGAGGTTAACAAGATGACTCGGTCGTCCGTTGACCGACCTCGGACCTCGGTTCTCGCCCGGCGAGGAGTC
TCGCTTGACGTGTCTCGAAACCAGTCCACGAGCTCGACGGCCGCTCACTTGCGGCCCCAGCACGATCGTCTGGAC
TTTCTCAACGATCCTGCCATGCACGATGAGTCCGAGGTTTTCAACCGGTGCTTCAGGCACCTGGATGACTTCGCC
ACAGAAGGTCTCAGGACCCTTGTCTATGCTCAAAGGTTTATCTCGGATTCGGAATACCGCACGTGGAAGAAACTC
TACGACGAGGCGACGACGAGCCTTCACGACCGACAGGTAATGATAGAGGCCGCCGGTGAGCTGATTGAGACAAGT
CTCGAACTCGTCGGCGCCACCGCCATCGAAGACAAGCTGCAAAAGGGCGTCCCGGAGACTATAGACAGACTGCGA
CGGGCCAACATCAAGATCTGGATGGTGACGGGTGATAAGCGTGAGACGGCCATCAATATTGCCCACTCGGCGCGC
ATCTGCCGACCGGGATCCGACCTCTACGTCCTGGATGTGGACAGAAGTCTTCTGGAGACGCAGCTCGTGGCCCTG
GCCGAGGATTTGCAGGCCGGTTCCGTCCACAGCGTCGTCGTCATCGACGGGCAGACGCTGGCCGCGGTGGAGAAG
TCGGCCGAGCTGTCGAGACGCTTCTTCAGCCTGGCCATGACGGTCGACTCCGTAATCTGCTGTCGGGCGTCGCCG
GCGCAGAAGGCGATACTGGTCCGGGCCGTGCGCGCGCGCCTGGGTACCCTAAAAGACAAGGACCGGCGCGGGCTT
ACGCTGGCCATCGGCGACGGCGCAAATGATCTCGCCATGATCCAGGCCAGCCACGTCGGTGTCGGCATATCCGGA
AAGGAGGGCCTCCAGGCGGCGCGCGTGGCCGACTATGCCATCGCCCAGTTCCGCTTCCTACAGCGGCTGCTCCTC
GTCCACGGTCGCTGGAACTACGTGCGGACGGCAAAGTTTATCCTTTGCACCTTTTGGAAGGAGATGTTCTTCTAT
CTGCCGACGGCCATATACCAGAGATGCAGCGGCTACAGCGGCACCTCGTTGTACCAGGAGGTGAGCCTGACCGTC
TTCAACACGCTCTTCACCAGCCTCTGCACCATCTGCATGGGCGTCTGGGAGCAGGACTTGAGCGCCGAGACGCTG
CTGGCCGTGCCCGAGCTGTACGTCTACGGCCAACGCGGCCTGGGGCTCAACATGTCCAAGTATCTGCGCTGGATG
GCCGTGGCCGCTGTCCAAGGTTTGGCCGTCTGGTACGGCGTCTGGGCCGGATACGGCATCGTCTCGCCGTCGGCT
CACGACGAGGGCCTCTACGCGCTGGGGACGCTGGCCTTTACCGTCGGCGTCTTGTGGATCAACTGGAAGCTATTG
TGA
Gene >Ophio5|5222
ATGTCTTCCGCCTCGTTACCCGAGAAGGCTCCCGCGTTCCTCGTCTCGAGTCCGCATCGTCCCTTCGATGACGAC
GACCCCGGCCCTCGTCTGCCTCTGCGAAACCGCTTCTGGGCCGCCCTACAGTCGCTTTACCAGGCTACCATCGTC
CATCTGATACTGCGCAAGAAGCACATCGACGCCACCAAGCATGGCAGGCACATTCCACTTGCCATTGACCACCAA
AAGCCGCTCATCGACACCCGCCGCGGCCACGCCTATCTTTCCAACGATGTCCGCACCTCTCGCTATACCATATGG
GACTTTATACCCAAGCAATTCTTCTTTCAGTTTTCCCGTGTCGGAAACTTTTACTTCCTCTGCGTCGGCATCCCC
CAGACGGTATGTGACACCCCTTACTCTCTTCCCCCTTTCGTCTTGAGCTGACCCAACTTCAGATACCGGGCCTGT
CCACGACGGGCTCCTTTACCACCATTTTACCTTTATTGTTCTTCGTCCTCCTCACCGTGGCCAAGGAGGGCTATG
ATGACTACAGACGGCATCTCTTGGACAAGGTTGAGAATGCAAACTTCGTCACTGTCCTCGGCCGCCATGACCTGA
GTGTCGTCCATGCCAGGTCGTCTCGTTCTTGGCGCCGCTGGGTCTCCTTTCGCACCGAATCCACCAGCCAGCCAA
GGCCGTCGCTCCCCAAAGATGAGTACCTCGGCGTTCGATGGGTGCCCTCTCGATGGAGTCACGTCAAGGTTGGAG
ACGTCGTCTTGCTGTCCCGCGACGAACCGGTCCCCGCCGACTTGGTCCTTCTTCATAGTGATGGCGAGAACGGCA
TTGCCTACATCGACACCATGGCCTTGGACGGCGAAACCAGTCTCAAGACGAAGCAGGTTTGCCACGCCCTTCACG
GATGTGGCTCTATCCAGGGCATTGCCGAATGCCGGGCCGAGTTCGTCGTCGAGGACCCGAATCCAGACCTTTTCA
ACTTCAATGGCCGCGTCACCGTCCGGGACAAAACCGTGCCCCTGACCCTCAGCCATGTCGTCTACCGGGGCAGCG
TTGTGCGGAACACGACCCGCGCCATCGGTCTCGTTGTCAACACGGGTGAGGAGTGCAAGGTCCGCATGAACTCCA
ACCAACACCCGCGTGCGAAGCGGCCGGCCCTCGAGAAGATCGTCAACAAGGTCGTCCTGACCCTGGCAATTTACG
TCCTTGTCCTCTCCGTCGGCGTCTCCATGGGCTATGTTCACTTTCGTGCCGACTACGAGAAGCATGCCTGGTTCC
TCGACGGCGCCACAGTCCCGTTTCACCAGATCATCATCGCCTTCGTCATCATGTTCAACAACATTGTACCCCTAT
CCTTGTATATATCACTGGAAATTGTCAAGGTCGGCCAGCTTCTTCTACTCAACTCTGACGTCGAAATGTACGACG
AGGAGACGGACACGCCGGCGCGATGTAATACCAACACCATCATGGAAAACCTCGGCCAAATTGGCTACGTCTTCT
CCGACAAGACGGGAACTCTGACGGACAACGTCATGAGGTTCCGCAAGCTCAGCGTCGCCGGCACCGTCTGGCTTC
ACGCCATGGACCTCGAGCAGCCCGAGACCGACGGGCCTCCGACGCCCTCTTCGCTCGACCGGCATTCGGTTCGGA
AGCCGACGGTGAGCAAGGCCTCGGCCATCCCCGAGGACGAACGCAAAACCCCGACGTTGGCATCGCGGTCATCGC
TGGGCCGGAGGCCATCGTCACAATGGCGTTCCACCGGTCGCCCAGACCTCGTACAGCCCGAGGTCAACACGTCAG
ATCTCCTGGAGCACATGAGGCTCCGGCCGCATTCCGCCTTCTCCAGGACAGCCAGAGACTATTTGCTCGCCGTCG
CCATCTGCCACACTTGCCTGCCCGAAGTCAAGAACGGAAGGATCGAGTTCCAGGCGTCTTCGCCCGATGAGCTGG
CTCTAGTGAGAGCAGCTCAGGAGCTTGGCTTTGGCGTGACCCATCGCACGTCGCAAAGCATAACACTGCAGGTTT
CGCGGCCCAGCGGCCAGAGCGAGAAGATGGTTTTCCAGATTCTGGACGTCATCGAGTTTAGCAGCACGCGCAAGA
GAATGTCCATTGTCGTTCGCTATCCCGATGGGCGCACATCCATCGTATGCAAAGGCGCCGACTCGGTCATTCTGC
CTAGGCTCAGGCTGTCCACTCTGGCGATGCAGAGGGCACACGAGGTCCGGAAGAGTGCCGACCTCGAGCGCGAGA
TGCAGCGGCGCAGCGAGCAGCAGGAGCCCCGGAACAGCTTTGGCGGGAGGCGAAGCCTGACCGTCTGGCGAAACG
CCGAAGTCGCGACTGATGCTAGCGGAGGCCGGCGCTCACTGGCCAGCCGCAGCAGATCTTTCGAGGTTAACAAGA
TGACTCGGTCGTCCGTTGACCGACCTCGGACCTCGGTTCTCGCCCGGCGAGGAGTCTCGCTTGACGTGTCTCGAA
ACCAGTCCACGAGCTCGACGGCCGCTCACTTGCGGCCCCAGCACGATCGTCTGGACTTTCTCAACGATCCTGCCA
TGCACGATGAGTCCGAGGTTTTCAACCGGTGCTTCAGGCACCTGGATGACTTCGCCACAGAAGGTCTCAGGACCC
TTGTCTATGCTCAAAGGTTTATCTCGGATTCGGAATACCGCACGTGGAAGAAACTCTACGACGAGGCGACGACGA
GCCTTCACGACCGACAGGTAATGATAGAGGCCGCCGGTGAGCTGATTGAGACAAGTCTCGAACTCGTCGGCGCCA
CCGCCATCGAAGACAAGCTGCAAAAGGGCGTCCCGGAGACTATAGACAGACTGCGACGGGCCAACATCAAGATCT
GGATGGTGACGGGTGATAAGCGTGAGACGGCCATCAATATTGCCCACTCGGCGCGCATCTGCCGACCGGGATCCG
ACCTCTACGTCCTGGATGTGGACAGAAGTCTTCTGGAGACGCAGCTCGTGGCCCTGGCCGAGGATTTGCAGGCCG
GTTCCGTCCACAGCGTCGTCGTCATCGACGGGCAGACGCTGGCCGCGGTGGAGAAGTCGGCCGAGCTGTCGAGAC
GCTTCTTCAGCCTGGCCATGACGGTCGACTCCGTAATCTGCTGTCGGGCGTCGCCGGCGCAGAAGGCGATACTGG
TCCGGGCCGTGCGCGCGCGCCTGGGTACCCTAAAAGACAAGGACCGGCGCGGGCTTACGCTGGCCATCGGCGACG
GCGCAAATGATCTCGCCATGATCCAGGCCAGCCACGTCGGTGTCGGCATATCCGGAAAGGAGGGCCTCCAGGCGG
CGCGCGTGGCCGACTATGCCATCGCCCAGTTCCGCTTCCTACAGCGGCTGCTCCTCGTCCACGGTCGCTGGAACT
ACGTGCGGACGGCAAAGTTTATCCTTTGCACCTTTTGGAAGGAGATGTTCTTCTATCTGCCGACGGCCATATACC
AGAGATGCAGCGGCTACAGCGGCACCTCGTTGTACCAGGAGGTGAGCCTGACCGTCTTCAACACGCTCTTCACCA
GCCTCTGCACCATCTGCATGGGCGTCTGGGAGCAGGACTTGAGCGCCGAGACGCTGCTGGCCGTGCCCGAGCTGT
ACGTCTACGGCCAACGCGGCCTGGGGCTCAACATGTCCAAGTATCTGCGCTGGATGGCCGTGGCCGCTGTCCAAG
GTTTGGCCGTCTGGTACGGCGTCTGGGCCGGATACGGCATCGTCTCGCCGTCGGCTCACGACGAGGGCCTCTACG
CGCTGGGGACGCTGGCCTTTACCGTCGGCGTCTTGTGGATCAACTGGAAGCTATTGTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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