Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|738
Gene name
LocationContig_115:31675..36463
Strand+
Gene length (bp)4788
Transcript length (bp)4437
Coding sequence length (bp)4437
Protein length (aa) 1479

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00271 Helicase_C Helicase conserved C-terminal domain 5.8E-14 944 1066
PF04408 HA2 Helicase associated domain (HA2) 1.9E-13 1131 1214
PF00270 DEAD DEAD/DEAH box helicase 2.8E-11 683 838
PF07717 OB_NTP_bind Oligonucleotide/oligosaccharide-binding (OB)-fold 4.3E-08 1321 1398
PF13401 AAA_22 AAA domain 1.4E-07 689 834

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|O60114|YG65_SCHPO Uncharacterized helicase C15C4.05 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC15C4.05 PE=3 SV=1 6 1464 0.0E+00
sp|Q7Z478|DHX29_HUMAN ATP-dependent RNA helicase DHX29 OS=Homo sapiens GN=DHX29 PE=1 SV=2 501 1446 0.0E+00
sp|A3KMI0|DHX29_XENLA ATP-dependent RNA helicase DHX29 OS=Xenopus laevis GN=dhx29 PE=2 SV=1 455 1446 0.0E+00
sp|Q6PGC1|DHX29_MOUSE ATP-dependent RNA helicase Dhx29 OS=Mus musculus GN=Dhx29 PE=1 SV=1 501 1446 1.0E-175
sp|Q6P158|DHX57_HUMAN Putative ATP-dependent RNA helicase DHX57 OS=Homo sapiens GN=DHX57 PE=1 SV=2 658 1447 5.0E-164
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|O60114|YG65_SCHPO Uncharacterized helicase C15C4.05 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC15C4.05 PE=3 SV=1 6 1464 0.0E+00
sp|Q7Z478|DHX29_HUMAN ATP-dependent RNA helicase DHX29 OS=Homo sapiens GN=DHX29 PE=1 SV=2 501 1446 0.0E+00
sp|A3KMI0|DHX29_XENLA ATP-dependent RNA helicase DHX29 OS=Xenopus laevis GN=dhx29 PE=2 SV=1 455 1446 0.0E+00
sp|Q6PGC1|DHX29_MOUSE ATP-dependent RNA helicase Dhx29 OS=Mus musculus GN=Dhx29 PE=1 SV=1 501 1446 1.0E-175
sp|Q6P158|DHX57_HUMAN Putative ATP-dependent RNA helicase DHX57 OS=Homo sapiens GN=DHX57 PE=1 SV=2 658 1447 5.0E-164
sp|Q6P5D3|DHX57_MOUSE Putative ATP-dependent RNA helicase DHX57 OS=Mus musculus GN=Dhx57 PE=1 SV=2 658 1446 4.0E-163
sp|F4I9Q5|DEXH7_ARATH DExH-box ATP-dependent RNA helicase DExH7, chloroplastic OS=Arabidopsis thaliana GN=At1g58060 PE=2 SV=1 657 1455 1.0E-160
sp|Q8VHK9|DHX36_MOUSE ATP-dependent RNA helicase DHX36 OS=Mus musculus GN=Dhx36 PE=1 SV=2 663 1446 4.0E-155
sp|Q9H2U1|DHX36_HUMAN ATP-dependent RNA helicase DHX36 OS=Homo sapiens GN=DHX36 PE=1 SV=2 642 1446 1.0E-152
sp|F4ILR7|DEXH1_ARATH DExH-box ATP-dependent RNA helicase DExH1 OS=Arabidopsis thaliana GN=At2g35920 PE=2 SV=1 671 1446 1.0E-144
sp|Q9C6G0|DEXH4_ARATH DExH-box ATP-dependent RNA helicase DExH4, chloroplastic OS=Arabidopsis thaliana GN=At1g58050 PE=3 SV=1 640 1455 3.0E-142
sp|F4IM84|DEXH5_ARATH DExH-box ATP-dependent RNA helicase DExH5, mitochondrial OS=Arabidopsis thaliana GN=At2g01130 PE=3 SV=1 665 1446 5.0E-133
sp|F4HYJ7|DEXH3_ARATH DExH-box ATP-dependent RNA helicase DExH3 OS=Arabidopsis thaliana GN=At1g48650 PE=2 SV=1 655 1446 8.0E-131
sp|P0C7L7|YUM14_USTMA Putative DEAH-box ATP-dependent helicase UM11114 OS=Ustilago maydis (strain 521 / FGSC 9021) GN=UMAG_11114 PE=3 SV=1 661 1468 5.0E-117
sp|P24785|MLE_DROME Dosage compensation regulator OS=Drosophila melanogaster GN=mle PE=1 SV=2 658 1446 8.0E-113
sp|Q7L2E3|DHX30_HUMAN Putative ATP-dependent RNA helicase DHX30 OS=Homo sapiens GN=DHX30 PE=1 SV=1 665 1444 3.0E-109
sp|Q5ZI74|DHX30_CHICK Putative ATP-dependent RNA helicase DHX30 OS=Gallus gallus GN=DHX30 PE=2 SV=1 674 1474 1.0E-108
sp|Q28141|DHX9_BOVIN ATP-dependent RNA helicase A OS=Bos taurus GN=DHX9 PE=2 SV=1 664 1450 2.0E-108
sp|Q5R607|DHX30_PONAB Putative ATP-dependent RNA helicase DHX30 OS=Pongo abelii GN=DHX30 PE=2 SV=1 665 1444 1.0E-107
sp|Q2NKY8|DHX30_BOVIN Putative ATP-dependent RNA helicase DHX30 OS=Bos taurus GN=DHX30 PE=2 SV=1 665 1421 1.0E-107
sp|Q08211|DHX9_HUMAN ATP-dependent RNA helicase A OS=Homo sapiens GN=DHX9 PE=1 SV=4 662 1450 2.0E-107
sp|Q5R874|DHX9_PONAB ATP-dependent RNA helicase A OS=Pongo abelii GN=DHX9 PE=2 SV=1 662 1450 2.0E-107
sp|Q5BJS0|DHX30_RAT Putative ATP-dependent RNA helicase DHX30 OS=Rattus norvegicus GN=Dhx30 PE=1 SV=1 665 1421 3.0E-107
sp|Q99PU8|DHX30_MOUSE Putative ATP-dependent RNA helicase DHX30 OS=Mus musculus GN=Dhx30 PE=1 SV=1 665 1444 3.0E-107
sp|O94536|UCP12_SCHPO Putative ATP-dependent RNA helicase ucp12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ucp12 PE=3 SV=1 655 1432 2.0E-103
sp|O70133|DHX9_MOUSE ATP-dependent RNA helicase A OS=Mus musculus GN=Dhx9 PE=1 SV=2 662 1450 3.0E-103
sp|Q68FK8|DHX9_XENLA ATP-dependent RNA helicase A-like protein OS=Xenopus laevis GN=dhx9 PE=2 SV=1 663 1460 1.0E-100
sp|Q14147|DHX34_HUMAN Probable ATP-dependent RNA helicase DHX34 OS=Homo sapiens GN=DHX34 PE=1 SV=2 655 1315 4.0E-99
sp|Q06698|YL419_YEAST Putative ATP-dependent RNA helicase YLR419W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YLR419W PE=1 SV=1 617 1277 2.0E-97
sp|B8A4F4|TDRD9_DANRE Putative ATP-dependent RNA helicase TDRD9 OS=Danio rerio GN=tdrd9 PE=2 SV=1 631 1226 8.0E-93
sp|Q8NDG6|TDRD9_HUMAN Putative ATP-dependent RNA helicase TDRD9 OS=Homo sapiens GN=TDRD9 PE=2 SV=3 674 1265 9.0E-89
sp|Q3MHU3|TDRD9_RAT Putative ATP-dependent RNA helicase TDRD9 OS=Rattus norvegicus GN=Tdrd9 PE=2 SV=3 674 1265 2.0E-88
sp|Q22307|DHX9_CAEEL Probable ATP-dependent RNA helicase A OS=Caenorhabditis elegans GN=rha-1 PE=2 SV=3 671 1269 3.0E-88
sp|B0XDC4|SPNE_CULQU Probable ATP-dependent RNA helicase spindle-E OS=Culex quinquefasciatus GN=spn-E PE=3 SV=1 674 1341 3.0E-88
sp|Q14BI7|TDRD9_MOUSE Putative ATP-dependent RNA helicase TDRD9 OS=Mus musculus GN=Tdrd9 PE=1 SV=3 674 1265 6.0E-87
sp|Q7QCW2|SPNE_ANOGA Probable ATP-dependent RNA helicase spindle-E OS=Anopheles gambiae GN=spn-E PE=3 SV=5 673 1332 2.0E-85
sp|Q20875|DHX15_CAEEL Pre-mRNA-splicing factor ATP-dependent RNA helicase ddx-15 OS=Caenorhabditis elegans GN=ddx-15 PE=3 SV=1 639 1265 2.0E-85
sp|Q10752|CDC28_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase-like protein cdc28 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=cdc28 PE=3 SV=2 656 1389 1.0E-84
sp|Q54MH3|DHX16_DICDI Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Dictyostelium discoideum GN=dhx16 PE=3 SV=1 666 1373 1.0E-84
sp|Q16JS8|SPNE_AEDAE Probable ATP-dependent RNA helicase spindle-E OS=Aedes aegypti GN=spn-E PE=3 SV=1 673 1341 3.0E-84
sp|Q296Q5|SPNE_DROPS Probable ATP-dependent RNA helicase spindle-E OS=Drosophila pseudoobscura pseudoobscura GN=spn-E PE=3 SV=2 647 1344 1.0E-83
sp|B4HLH4|SPNE_DROSE Probable ATP-dependent RNA helicase spindle-E OS=Drosophila sechellia GN=spn-E PE=3 SV=1 649 1226 3.0E-82
sp|B4GEU5|SPNE_DROPE Probable ATP-dependent RNA helicase spindle-E OS=Drosophila persimilis GN=spn-E PE=3 SV=1 647 1261 4.0E-82
sp|B4LX81|SPNE_DROVI Probable ATP-dependent RNA helicase spindle-E OS=Drosophila virilis GN=spn-E PE=3 SV=1 650 1231 5.0E-82
sp|P53131|PRP43_YEAST Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP43 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PRP43 PE=1 SV=1 604 1389 7.0E-82
sp|P24384|PRP22_YEAST Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP22 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PRP22 PE=1 SV=1 650 1389 1.0E-81
sp|Q9VF26|SPNE_DROME Probable ATP-dependent RNA helicase spindle-E OS=Drosophila melanogaster GN=spn-E PE=2 SV=1 649 1229 2.0E-80
sp|B4PRJ9|SPNE_DROYA Probable ATP-dependent RNA helicase spindle-E OS=Drosophila yakuba GN=spn-E PE=3 SV=1 649 1226 1.0E-79
sp|B4NBB0|SPNE_DROWI Probable ATP-dependent RNA helicase spindle-E OS=Drosophila willistoni GN=spn-E PE=3 SV=1 657 1232 4.0E-79
sp|B4JT42|SPNE_DROGR Probable ATP-dependent RNA helicase spindle-E OS=Drosophila grimshawi GN=spn-E PE=3 SV=1 649 1232 8.0E-79
sp|B3P3W1|SPNE_DROER Probable ATP-dependent RNA helicase spindle-E OS=Drosophila erecta GN=spn-E PE=3 SV=1 649 1226 5.0E-78
sp|F4JMJ3|DEAH8_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH8 OS=Arabidopsis thaliana GN=At4g16680 PE=2 SV=2 669 1389 1.0E-77
sp|B4K5R2|SPNE_DROMO Probable ATP-dependent RNA helicase spindle-E OS=Drosophila mojavensis GN=spn-E PE=3 SV=1 650 1231 2.0E-77
sp|B3M383|SPNE_DROAN Probable ATP-dependent RNA helicase spindle-E OS=Drosophila ananassae GN=spn-E PE=3 SV=1 649 1229 3.0E-76
sp|P15938|PRP16_YEAST Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PRP16 PE=1 SV=2 670 1390 3.0E-75
sp|F4JRJ6|DEAH9_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH9 OS=Arabidopsis thaliana GN=At4g18465 PE=3 SV=1 662 1385 1.0E-72
sp|Q03319|PRH1_SCHPO Probable ATP-dependent RNA helicase prh1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prh1 PE=3 SV=2 663 1379 4.0E-71
sp|P43329|HRPA_ECOLI ATP-dependent RNA helicase HrpA OS=Escherichia coli (strain K12) GN=hrpA PE=3 SV=3 674 1274 2.0E-70
sp|Q80VY9|DHX33_MOUSE Putative ATP-dependent RNA helicase DHX33 OS=Mus musculus GN=Dhx33 PE=1 SV=1 671 1265 5.0E-69
sp|B2RR83|YTDC2_MOUSE Probable ATP-dependent RNA helicase YTHDC2 OS=Mus musculus GN=Ythdc2 PE=1 SV=1 887 1400 1.0E-68
sp|Q9H6R0|DHX33_HUMAN Putative ATP-dependent RNA helicase DHX33 OS=Homo sapiens GN=DHX33 PE=1 SV=2 671 1265 5.0E-68
sp|Q9HE06|YK99_SCHPO Putative pre-mRNA-splicing factor ATP-dependent RNA helicase C20H4.09 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC20H4.09 PE=3 SV=1 674 1269 6.0E-68
sp|Q9H6S0|YTDC2_HUMAN Probable ATP-dependent RNA helicase YTHDC2 OS=Homo sapiens GN=YTHDC2 PE=1 SV=2 922 1400 9.0E-68
sp|P45018|HRPA_HAEIN ATP-dependent RNA helicase HrpA homolog OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=hrpA PE=3 SV=2 674 1251 2.0E-66
sp|Q9BKQ8|DHX35_CAEEL Probable ATP-dependent RNA helicase DHX35 homolog OS=Caenorhabditis elegans GN=Y67D2.6 PE=3 SV=1 606 1285 2.0E-65
sp|Q8IX18|DHX40_HUMAN Probable ATP-dependent RNA helicase DHX40 OS=Homo sapiens GN=DHX40 PE=1 SV=2 674 1379 3.0E-64
sp|Q5RBD4|DHX35_PONAB Probable ATP-dependent RNA helicase DHX35 OS=Pongo abelii GN=DHX35 PE=2 SV=1 669 1388 1.0E-63
sp|Q9H5Z1|DHX35_HUMAN Probable ATP-dependent RNA helicase DHX35 OS=Homo sapiens GN=DHX35 PE=1 SV=2 669 1388 1.0E-63
sp|P36009|DHR2_YEAST Probable ATP-dependent RNA helicase DHR2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DHR2 PE=1 SV=1 652 1212 5.0E-63
sp|P20095|PRP2_YEAST Pre-mRNA-splicing factor ATP-dependent RNA helicase-like protein PRP2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PRP2 PE=1 SV=1 666 1357 4.0E-61
sp|F4IE66|PRP22_ARATH Pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH10 OS=Arabidopsis thaliana GN=RID1 PE=1 SV=1 665 1274 3.0E-60
sp|Q5R864|DHX40_PONAB Probable ATP-dependent RNA helicase DHX40 OS=Pongo abelii GN=DHX40 PE=2 SV=1 674 1379 2.0E-59
sp|O17438|DHX15_STRPU Putative pre-mRNA-splicing factor ATP-dependent RNA helicase PRP1 (Fragment) OS=Strongylocentrotus purpuratus GN=PRP1 PE=2 SV=1 777 1278 2.0E-59
sp|Q5XI69|DHX40_RAT Probable ATP-dependent RNA helicase DHX40 OS=Rattus norvegicus GN=Dhx40 PE=2 SV=1 674 1379 3.0E-59
sp|Q6PE54|DHX40_MOUSE Probable ATP-dependent RNA helicase DHX40 OS=Mus musculus GN=Dhx40 PE=1 SV=1 674 1379 9.0E-59
sp|Q9HDY4|YK16_SCHPO Putative ATP-dependent RNA helicase PB1A10.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAPB1A10.06c PE=3 SV=1 669 1269 2.0E-58
sp|F4INY4|HVT1_ARATH DExH-box ATP-dependent RNA helicase DExH6 OS=Arabidopsis thaliana GN=HVT1 PE=2 SV=1 919 1275 7.0E-58
sp|F4KGU4|DEAHC_ARATH ATP-dependent RNA helicase DEAH12, chloroplastic OS=Arabidopsis thaliana GN=At5g10370 PE=3 SV=1 674 1265 4.0E-57
sp|F4IDQ6|NIH_ARATH DExH-box ATP-dependent RNA helicase DExH2 OS=Arabidopsis thaliana GN=NIH PE=1 SV=1 893 1275 8.0E-57
sp|Q04217|DHR1_YEAST Probable ATP-dependent RNA helicase DHR1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ECM16 PE=1 SV=1 652 1196 3.0E-55
sp|F4IDQ6|NIH_ARATH DExH-box ATP-dependent RNA helicase DExH2 OS=Arabidopsis thaliana GN=NIH PE=1 SV=1 664 870 7.0E-55
sp|P0CE10|DEAHB_ARATH ATP-dependent RNA helicase DEAH11, chloroplastic OS=Arabidopsis thaliana GN=At4g01020 PE=3 SV=1 674 1265 7.0E-55
sp|F4INY4|HVT1_ARATH DExH-box ATP-dependent RNA helicase DExH6 OS=Arabidopsis thaliana GN=HVT1 PE=2 SV=1 671 891 1.0E-51
sp|Q17R09|PRP16_BOVIN Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 OS=Bos taurus GN=DHX38 PE=2 SV=1 634 1265 4.0E-51
sp|Q1EHT7|C3H4_ORYSJ Zinc finger CCCH domain-containing protein 4 OS=Oryza sativa subsp. japonica GN=Os01g0256800 PE=2 SV=1 669 1269 8.0E-51
sp|Q9DBV3|DHX34_MOUSE Probable ATP-dependent RNA helicase DHX34 OS=Mus musculus GN=Dhx34 PE=1 SV=2 953 1297 1.0E-50
sp|F4K2E9|PRP16_ARATH Pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH7 OS=Arabidopsis thaliana GN=CUV PE=1 SV=1 665 1269 9.0E-48
sp|Q92620|PRP16_HUMAN Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 OS=Homo sapiens GN=DHX38 PE=1 SV=2 663 1265 9.0E-47
sp|O42945|DHX15_SCHPO Probable pre-mRNA-splicing factor ATP-dependent RNA helicase prp43 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp43 PE=3 SV=1 654 868 6.0E-46
sp|F4IJV4|DEAH6_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH6 OS=Arabidopsis thaliana GN=MEE29 PE=2 SV=1 639 865 7.0E-46
sp|Q9H6S0|YTDC2_HUMAN Probable ATP-dependent RNA helicase YTHDC2 OS=Homo sapiens GN=YTHDC2 PE=1 SV=2 658 927 7.0E-45
sp|B2RR83|YTDC2_MOUSE Probable ATP-dependent RNA helicase YTHDC2 OS=Mus musculus GN=Ythdc2 PE=1 SV=1 658 876 1.0E-44
sp|Q9DBV3|DHX34_MOUSE Probable ATP-dependent RNA helicase DHX34 OS=Mus musculus GN=Dhx34 PE=1 SV=2 655 865 2.0E-44
sp|O22243|C3H31_ARATH DExH-box ATP-dependent RNA helicase DExH8 OS=Arabidopsis thaliana GN=At2g47680 PE=2 SV=2 672 1229 1.0E-43
sp|Q8VY00|ESP3_ARATH Pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH1 OS=Arabidopsis thaliana GN=ESP3 PE=1 SV=1 664 865 3.0E-43
sp|O45244|DHX16_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-4 OS=Caenorhabditis elegans GN=mog-4 PE=1 SV=2 663 865 4.0E-43
sp|Q8VY00|ESP3_ARATH Pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH1 OS=Arabidopsis thaliana GN=ESP3 PE=1 SV=1 953 1389 6.0E-43
sp|F4IJV4|DEAH6_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH6 OS=Arabidopsis thaliana GN=MEE29 PE=2 SV=1 952 1389 3.0E-42
sp|O60231|DHX16_HUMAN Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Homo sapiens GN=DHX16 PE=1 SV=2 953 1373 3.0E-42
sp|Q7YR39|DHX16_PANTR Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Pan troglodytes GN=DHX16 PE=3 SV=1 953 1373 3.0E-42
sp|Q767K6|DHX16_PIG Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Sus scrofa GN=DHX16 PE=3 SV=1 953 1373 4.0E-42
sp|Q9P774|PRP16_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase prp16 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp16 PE=3 SV=2 669 872 5.0E-42
sp|Q14562|DHX8_HUMAN ATP-dependent RNA helicase DHX8 OS=Homo sapiens GN=DHX8 PE=1 SV=1 660 868 5.0E-42
sp|O42643|PRP22_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase prp22 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp22 PE=1 SV=1 660 865 6.0E-42
sp|A2A4P0|DHX8_MOUSE ATP-dependent RNA helicase DHX8 OS=Mus musculus GN=Dhx8 PE=2 SV=1 660 868 6.0E-42
sp|Q38953|DEAH5_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH5 OS=Arabidopsis thaliana GN=At3g26560 PE=1 SV=2 927 1389 7.0E-42
sp|O22899|PRP43_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH3 OS=Arabidopsis thaliana GN=At2g47250 PE=2 SV=1 655 868 7.0E-42
sp|Q54NJ4|DHX15_DICDI Putative pre-mRNA-splicing factor ATP-dependent RNA helicase dhx15 OS=Dictyostelium discoideum GN=dhx15 PE=3 SV=1 655 869 1.0E-41
sp|Q5RAZ4|DHX15_PONAB Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Pongo abelii GN=DHX15 PE=2 SV=2 953 1379 2.0E-41
sp|O35286|DHX15_MOUSE Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Mus musculus GN=Dhx15 PE=1 SV=2 953 1379 2.0E-41
sp|O43143|DHX15_HUMAN Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Homo sapiens GN=DHX15 PE=1 SV=2 953 1379 2.0E-41
sp|P34498|MOG1_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-1 OS=Caenorhabditis elegans GN=mog-1 PE=1 SV=2 665 872 2.0E-40
sp|Q09530|MOG5_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-5 OS=Caenorhabditis elegans GN=mog-5 PE=1 SV=1 666 865 2.0E-40
sp|Q54F05|DHX8_DICDI ATP-dependent RNA helicase dhx8 OS=Dictyostelium discoideum GN=dhx8 PE=3 SV=1 634 868 2.0E-40
sp|Q767K6|DHX16_PIG Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Sus scrofa GN=DHX16 PE=3 SV=1 671 888 3.0E-40
sp|Q38953|DEAH5_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH5 OS=Arabidopsis thaliana GN=At3g26560 PE=1 SV=2 669 865 3.0E-40
sp|O60231|DHX16_HUMAN Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Homo sapiens GN=DHX16 PE=1 SV=2 671 888 9.0E-40
sp|Q7YR39|DHX16_PANTR Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Pan troglodytes GN=DHX16 PE=3 SV=1 671 888 9.0E-40
sp|O42643|PRP22_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase prp22 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp22 PE=1 SV=1 953 1389 9.0E-40
sp|Q9LZQ9|DEAH2_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH2 OS=Arabidopsis thaliana GN=At3g62310 PE=2 SV=1 655 868 9.0E-40
sp|Q54F05|DHX8_DICDI ATP-dependent RNA helicase dhx8 OS=Dictyostelium discoideum GN=dhx8 PE=3 SV=1 953 1389 1.0E-39
sp|Q5RAZ4|DHX15_PONAB Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Pongo abelii GN=DHX15 PE=2 SV=2 663 865 2.0E-39
sp|O35286|DHX15_MOUSE Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Mus musculus GN=Dhx15 PE=1 SV=2 663 865 2.0E-39
sp|O43143|DHX15_HUMAN Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Homo sapiens GN=DHX15 PE=1 SV=2 663 865 2.0E-39
sp|Q14562|DHX8_HUMAN ATP-dependent RNA helicase DHX8 OS=Homo sapiens GN=DHX8 PE=1 SV=1 953 1389 3.0E-39
sp|A2A4P0|DHX8_MOUSE ATP-dependent RNA helicase DHX8 OS=Mus musculus GN=Dhx8 PE=2 SV=1 953 1389 4.0E-39
sp|Q93Y16|DEAH4_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH4 OS=Arabidopsis thaliana GN=At1g27900 PE=1 SV=1 672 865 2.0E-38
sp|O42945|DHX15_SCHPO Probable pre-mRNA-splicing factor ATP-dependent RNA helicase prp43 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp43 PE=3 SV=1 981 1389 3.0E-37
sp|O45244|DHX16_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-4 OS=Caenorhabditis elegans GN=mog-4 PE=1 SV=2 953 1269 4.0E-37
sp|O22899|PRP43_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH3 OS=Arabidopsis thaliana GN=At2g47250 PE=2 SV=1 953 1266 3.0E-36
sp|P34498|MOG1_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-1 OS=Caenorhabditis elegans GN=mog-1 PE=1 SV=2 953 1271 3.0E-36
sp|Q09530|MOG5_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-5 OS=Caenorhabditis elegans GN=mog-5 PE=1 SV=1 952 1389 6.0E-36
sp|Q54NJ4|DHX15_DICDI Putative pre-mRNA-splicing factor ATP-dependent RNA helicase dhx15 OS=Dictyostelium discoideum GN=dhx15 PE=3 SV=1 983 1265 9.0E-36
sp|Q9LZQ9|DEAH2_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH2 OS=Arabidopsis thaliana GN=At3g62310 PE=2 SV=1 953 1266 2.0E-35
sp|Q9P774|PRP16_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase prp16 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp16 PE=3 SV=2 945 1270 5.0E-35
sp|Q8IY37|DHX37_HUMAN Probable ATP-dependent RNA helicase DHX37 OS=Homo sapiens GN=DHX37 PE=1 SV=1 667 865 2.0E-30
sp|Q3ZBE0|DQX1_BOVIN ATP-dependent RNA helicase DQX1 OS=Bos taurus GN=DQX1 PE=2 SV=1 661 1313 2.0E-30
sp|Q5R746|YTDC2_PONAB YTH domain-containing protein 2 OS=Pongo abelii GN=YTHDC2 PE=2 SV=1 1084 1400 3.0E-30
sp|O46072|KZ_DROME Probable ATP-dependent RNA helicase kurz OS=Drosophila melanogaster GN=kz PE=1 SV=1 662 865 9.0E-30
sp|Q5UQ96|YL540_MIMIV Putative ATP-dependent RNA helicase L540 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_L540 PE=1 SV=1 643 1163 6.0E-29
sp|P37024|HRPB_ECOLI ATP-dependent RNA helicase HrpB OS=Escherichia coli (strain K12) GN=hrpB PE=3 SV=3 939 1168 7.0E-29
sp|P34305|RHA2_CAEEL Putative ATP-dependent RNA helicase rha-2 OS=Caenorhabditis elegans GN=rha-2 PE=3 SV=2 652 865 4.0E-28
sp|Q93Y16|DEAH4_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH4 OS=Arabidopsis thaliana GN=At1g27900 PE=1 SV=1 953 1246 9.0E-27
sp|Q9C813|DEAHD_ARATH ATP-dependent RNA helicase DEAH13 OS=Arabidopsis thaliana GN=FAS4 PE=2 SV=1 669 865 2.0E-26
sp|O46072|KZ_DROME Probable ATP-dependent RNA helicase kurz OS=Drosophila melanogaster GN=kz PE=1 SV=1 981 1265 2.0E-25
sp|P37024|HRPB_ECOLI ATP-dependent RNA helicase HrpB OS=Escherichia coli (strain K12) GN=hrpB PE=3 SV=3 674 866 3.0E-25
sp|Q924H9|DQX1_MOUSE ATP-dependent RNA helicase DQX1 OS=Mus musculus GN=Dqx1 PE=2 SV=1 661 1313 7.0E-24
sp|Q8V9U2|H962L_ASFM2 Putative RNA Helicase B962L OS=African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) GN=Mal-080 PE=3 SV=1 690 1151 1.0E-23
sp|P0C9A4|H962L_ASFK5 Putative RNA Helicase B962L OS=African swine fever virus (isolate Pig/Kenya/KEN-50/1950) GN=Ken-084 PE=3 SV=1 690 1157 1.0E-23
sp|Q8BZS9|DHX32_MOUSE Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Mus musculus GN=Dhx32 PE=1 SV=2 661 869 3.0E-23
sp|P0C9A2|H962L_ASFP4 Putative RNA Helicase B962L OS=African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) GN=Pret-084 PE=3 SV=1 690 1151 2.0E-22
sp|P0C9A3|H962L_ASFWA Putative RNA Helicase B962L OS=African swine fever virus (isolate Warthog/Namibia/Wart80/1980) GN=War-082 PE=3 SV=1 690 1151 2.0E-22
sp|Q89443|H962L_ASFB7 Putative RNA helicase B962L OS=African swine fever virus (strain Badajoz 1971 Vero-adapted) GN=Ba71V-072 PE=3 SV=1 690 1151 2.0E-22
sp|Q7L7V1|DHX32_HUMAN Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Homo sapiens GN=DHX32 PE=1 SV=1 661 869 3.0E-22
sp|Q8IY37|DHX37_HUMAN Probable ATP-dependent RNA helicase DHX37 OS=Homo sapiens GN=DHX37 PE=1 SV=1 981 1269 3.0E-21
sp|Q9C813|DEAHD_ARATH ATP-dependent RNA helicase DEAH13 OS=Arabidopsis thaliana GN=FAS4 PE=2 SV=1 981 1266 5.0E-19
sp|Q5XH12|DHX32_XENLA Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Xenopus laevis GN=dhx32 PE=2 SV=1 627 852 6.0E-19
sp|Q8TE96|DQX1_HUMAN ATP-dependent RNA helicase DQX1 OS=Homo sapiens GN=DQX1 PE=2 SV=2 661 855 3.0E-16
sp|Q8BZS9|DHX32_MOUSE Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Mus musculus GN=Dhx32 PE=1 SV=2 1005 1266 4.0E-16
sp|Q9W1I2|BGCN_DROME Benign gonial cell neoplasm protein OS=Drosophila melanogaster GN=bgcn PE=1 SV=2 885 1463 4.0E-16
sp|Q7L7V1|DHX32_HUMAN Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Homo sapiens GN=DHX32 PE=1 SV=1 1005 1266 3.0E-15
sp|P34305|RHA2_CAEEL Putative ATP-dependent RNA helicase rha-2 OS=Caenorhabditis elegans GN=rha-2 PE=3 SV=2 979 1192 3.0E-14
sp|Q5XH12|DHX32_XENLA Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Xenopus laevis GN=dhx32 PE=2 SV=1 1005 1266 6.0E-11
sp|Q8TE96|DQX1_HUMAN ATP-dependent RNA helicase DQX1 OS=Homo sapiens GN=DQX1 PE=2 SV=2 952 1313 8.0E-10
sp|Q9W1I2|BGCN_DROME Benign gonial cell neoplasm protein OS=Drosophila melanogaster GN=bgcn PE=1 SV=2 682 854 3.0E-09
sp|Q5UR20|YR366_MIMIV Putative ATP-dependent RNA helicase R366 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R366 PE=3 SV=1 1001 1104 8.0E-07
[Show less]

GO

GO Term Description Terminal node
GO:0004386 helicase activity Yes
GO:0003676 nucleic acid binding Yes
GO:0005524 ATP binding Yes
GO:0035639 purine ribonucleoside triphosphate binding No
GO:0032555 purine ribonucleotide binding No
GO:0005488 binding No
GO:0003824 catalytic activity No
GO:0036094 small molecule binding No
GO:1901363 heterocyclic compound binding No
GO:0097159 organic cyclic compound binding No
GO:0030554 adenyl nucleotide binding No
GO:1901265 nucleoside phosphate binding No
GO:0017076 purine nucleotide binding No
GO:0043167 ion binding No
GO:0032559 adenyl ribonucleotide binding No
GO:0000166 nucleotide binding No
GO:0140640 catalytic activity, acting on a nucleic acid No
GO:0043168 anion binding No
GO:0032553 ribonucleotide binding No
GO:0003674 molecular_function No
GO:0140657 ATP-dependent activity No
GO:0097367 carbohydrate derivative binding No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 11 0.45

Transmembrane Domains

(None)

Transcription Factor Class

(None)

Expression data

No expression data available for this genome

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 >Hirsu2|738
MAGTKKKKKPAVNPARGFATTSIASKPRPETEPQPSPTAQKSNDGDAPPSSAEDSASAPPAAQQQAGETPLSPEE
FERRLEEAELQLLVEKHAQKAKRDAQRQRQRLETDRRLLRNQADTVNIPKWLPPDLLDQILDLIKAETRFSASSV
SSENAGSGRMPSEEDMILRLWTLRQTLEAAAFPGERVEAALQHILDIAPHVSTAVKDSIWGLDEALDWLARQCSL
EELPAYESRPKPVARDTPTESPFSSRPHTPKPQDPQSSRGNKESSNGNGRAAKTPSKKTAVTFDADIEPEDLIPE
YIAAKAKLLELNRAHAMGKTRRHDAGNDDTDVEIAKQEAKLRKIDGDVLFDKFTAEQRWKVERVAVEKKLAAARQ
HAQQDQEPGASDPAAEAGKPDDDDISAEAERIAAEVLADQDEDDDDIAGLFASLPQDEVDPQTGKTRTVINSSSG
AKVVIRDFGDWTGIKPRRVLEEACRSRDASVKIHYSTVSEATFANRQSIDIGWAKPQEPPQSEPGSDVEIVADQN
RFTFTMVGIATPDAKQSEAYIATSALFHIFSGNAREEKVGLRLPPVWRDLWNELAEAKQSRLDSIDRDVVKSLRA
LVRQRHDQELEDGVILQGAFRGRGTPKAHQDAADSSLSDRKKQNSASGDEYKKIWADKSGSHKFQTMLESRAQLP
MWQFRPQVLDAVDKNQVVIICGETGCGKSTQVPSFLLEHELSQGKACKIYCTEPRRISAISLARRVSEELGEKKG
DLGTSRSLVGYSIRLEANTTRETRLVYATTGIVMRMLEGSNDLREVTHLVLDEVHERSIDSDFLLIVLKRLLAQR
KDLKVVLMSATVDAERFSRYLGRAPILNVPGRTFPVDVRYLEDAIEATGYSPTNSPADKMIDLDDDAMEEDAGNA
KSDAPQSLSAYSAKTRSALSQMDEYQIDFDLVVQLIAHVATSESLQQYSKATLVFLPGIAEIRTLNDMLLGDPRF
AKDCLVYPLHSTIATEDQESAFLVPPPGTRKIVLATNIAETGITIPDVTCVIDTGKHREMRYDERRQLSRLIDTF
ISRANAKQRRGRAGRVQNGLCFHLFTRHRHDNLMADQQTPEMLRLSLQDLAIRVKICKIGGIEETLGDALDPPSA
KNIRRAIDALVDVRALTMAEELTPLGHQLARLPLDVFLGKLILLGTVFKCLDMALTAAAILSSKSPFSAPFGQRA
QANNARMAFRRADSDLLTVYNAYLAWKRVCRSSGGGAGGREFQFCRKNFLSPQTLAGIEELKGQLLASLADSGFL
QLTEEERRALKGQRSGGGRGRRQQAFFEVPRRVDGNSDNDAVAASVVAWSFYPKLLVRDAPGARGLRNVGNNQSI
SLHPSSVNRGHLDIKWLAYYHIMQSKSVYHAHETTAVEPFAVALLCGDVRCDMFSGVIVLDGNRARFALPDWKSM
LVLKTLRARLRELLARAFRQPGRLATAQHEKWLDVWQRLFAAPEPPSGAAAKP*
Coding >Hirsu2|738
ATGGCCGGCACGAAGAAGAAGAAGAAGCCTGCCGTCAACCCGGCCCGGGGCTTCGCGACGACCTCGATCGCCTCC
AAGCCCAGGCCCGAGACGGAGCCCCAGCCGTCGCCGACCGCCCAAAAATCCAACGACGGCGATGCCCCTCCCTCG
TCGGCCGAGGACAGCGCCAGTGCCCCGCCGGCGGCCCAGCAGCAAGCTGGCGAAACGCCGCTGAGCCCCGAGGAG
TTCGAGAGGCGGCTCGAGGAGGCCGAGCTGCAGCTACTGGTCGAGAAGCACGCCCAGAAGGCCAAGCGCGACGCC
CAGCGCCAGCGCCAGCGCCTCGAGACGGACCGCCGCTTGCTGCGCAACCAGGCCGACACCGTCAACATCCCCAAG
TGGCTGCCCCCGGACCTGCTCGACCAGATCCTCGACCTGATAAAGGCCGAGACTCGCTTCTCTGCTTCGAGCGTC
TCGTCGGAAAATGCCGGGAGCGGCAGGATGCCCTCGGAGGAGGACATGATTCTCCGGCTGTGGACCCTGCGCCAA
ACTCTCGAGGCTGCTGCCTTCCCCGGCGAGAGAGTCGAGGCTGCGCTTCAGCACATCCTTGACATCGCTCCTCAC
GTGTCCACTGCCGTCAAGGACTCCATCTGGGGCCTGGACGAGGCCCTGGACTGGCTGGCGCGCCAATGCTCCCTT
GAGGAACTGCCGGCGTACGAGTCGCGCCCCAAGCCAGTCGCCAGAGATACGCCGACCGAAAGTCCGTTCTCGTCC
CGCCCGCATACGCCCAAGCCTCAAGATCCGCAGAGTAGTCGCGGGAATAAGGAATCAAGCAACGGCAACGGGCGC
GCCGCCAAGACGCCGTCCAAAAAGACGGCTGTGACTTTCGACGCCGACATCGAACCGGAGGACCTGATTCCCGAA
TACATCGCCGCCAAGGCAAAGCTTCTCGAGCTGAACCGTGCTCACGCTATGGGGAAGACCAGGCGCCATGACGCC
GGCAACGACGACACCGACGTGGAAATAGCAAAGCAGGAGGCCAAGCTGAGAAAAATCGACGGTGACGTGCTCTTC
GACAAATTCACAGCCGAGCAGCGCTGGAAGGTTGAGAGGGTGGCTGTGGAGAAAAAACTGGCGGCTGCGAGACAG
CACGCCCAGCAGGACCAAGAGCCCGGGGCATCGGATCCAGCCGCCGAGGCCGGAAAACCGGACGACGACGACATA
TCGGCCGAGGCGGAGCGCATCGCAGCCGAGGTCTTGGCCGACCAAGACGAAGACGACGATGATATTGCCGGTCTC
TTCGCGTCCCTGCCCCAGGACGAGGTTGACCCCCAGACCGGCAAGACACGAACCGTCATCAACTCCTCCAGCGGC
GCAAAGGTCGTGATACGGGACTTTGGCGATTGGACGGGTATCAAGCCTAGGAGGGTGCTGGAGGAGGCGTGTCGC
TCAAGGGATGCTTCCGTCAAAATCCACTACAGCACGGTGTCGGAGGCGACATTCGCGAATCGCCAGTCAATCGAC
ATCGGGTGGGCAAAGCCGCAGGAACCGCCCCAAAGTGAGCCCGGATCAGATGTGGAAATCGTTGCTGACCAAAAC
CGATTCACGTTCACGATGGTCGGGATCGCCACACCAGATGCTAAGCAGTCGGAAGCGTACATAGCCACCTCGGCT
CTCTTCCACATCTTCAGCGGCAATGCGAGGGAAGAAAAGGTCGGCCTGCGGTTGCCGCCTGTGTGGCGCGATTTA
TGGAACGAGTTGGCCGAGGCCAAGCAGAGTCGGCTGGACTCGATCGATCGCGACGTCGTCAAGTCCCTGAGGGCC
CTGGTCAGGCAGAGGCATGATCAGGAACTCGAAGATGGCGTCATCCTCCAAGGTGCCTTCCGAGGCCGGGGCACT
CCGAAAGCACATCAAGACGCAGCGGACAGCAGCCTGAGCGATCGCAAAAAGCAGAACTCGGCCAGCGGCGACGAG
TACAAAAAGATATGGGCCGACAAATCCGGCTCGCACAAATTTCAGACGATGCTGGAATCGAGGGCCCAGCTGCCC
ATGTGGCAGTTTCGGCCTCAAGTGCTCGATGCCGTAGACAAGAACCAGGTGGTCATCATCTGCGGCGAAACGGGA
TGTGGAAAGAGTACGCAAGTGCCGTCATTCCTGCTGGAGCACGAGCTCAGCCAAGGCAAAGCCTGCAAGATCTAC
TGCACGGAGCCGCGGCGTATCTCGGCCATATCGCTGGCCCGGCGAGTGAGCGAGGAGCTGGGCGAGAAGAAGGGC
GACCTGGGCACCAGCCGATCTCTCGTGGGCTACTCGATCCGCCTCGAGGCCAATACGACTCGCGAGACACGGCTG
GTGTACGCGACGACGGGTATCGTGATGCGCATGCTCGAAGGCTCCAACGACCTCCGCGAGGTGACGCATCTGGTG
CTCGACGAGGTGCACGAGCGGTCCATCGACAGCGACTTCCTCCTCATCGTCCTCAAGCGCCTGTTGGCGCAACGC
AAGGACCTCAAGGTGGTGCTCATGTCGGCCACGGTCGATGCCGAGCGCTTCTCGAGGTATCTCGGCCGGGCGCCG
ATCCTCAACGTGCCGGGACGGACGTTCCCCGTGGACGTGCGCTACCTCGAAGACGCCATCGAGGCGACCGGCTAC
AGCCCGACCAACTCGCCGGCCGACAAGATGATCGACCTGGACGACGACGCGATGGAGGAGGATGCCGGCAACGCG
AAGAGCGACGCGCCGCAGAGCCTATCCGCATATTCGGCCAAGACGCGCAGCGCGCTGTCGCAGATGGACGAGTAC
CAGATCGACTTCGACCTGGTCGTCCAGCTGATAGCCCACGTGGCCACAAGCGAGTCGCTGCAGCAGTACAGCAAG
GCAACGTTGGTCTTCCTGCCCGGCATCGCCGAGATCCGAACGCTGAACGACATGCTGCTCGGGGACCCGCGCTTC
GCAAAGGACTGCCTGGTGTATCCGCTGCATTCCACCATCGCGACCGAGGACCAGGAGTCGGCCTTCCTCGTGCCG
CCGCCCGGGACGCGCAAGATCGTGCTGGCGACCAACATAGCGGAAACGGGCATCACGATCCCGGACGTGACGTGC
GTCATCGACACGGGGAAGCACCGCGAGATGCGGTACGACGAGCGGAGGCAGCTGTCGAGGCTCATCGACACCTTC
ATCTCCCGGGCCAACGCGAAGCAGAGGCGGGGCCGTGCCGGGCGCGTGCAGAACGGCCTCTGCTTCCACCTGTTC
ACGCGGCACCGGCACGACAACCTGATGGCGGACCAGCAGACGCCGGAGATGCTGCGGCTGTCGCTGCAGGACCTC
GCGATCCGGGTCAAGATATGCAAAATCGGCGGCATCGAGGAGACGCTGGGGGACGCGCTGGACCCGCCGTCGGCC
AAGAACATACGGCGGGCGATCGACGCGCTCGTCGACGTGCGGGCGCTGACGATGGCGGAGGAGCTGACGCCGCTG
GGCCACCAGCTGGCGCGGCTGCCGCTCGACGTCTTCCTCGGCAAGCTGATCCTGCTCGGGACCGTCTTCAAGTGC
CTGGACATGGCGCTGACGGCGGCGGCGATCCTGTCGTCCAAGTCGCCCTTCTCGGCGCCCTTCGGGCAGCGGGCG
CAGGCCAACAACGCGCGCATGGCCTTCCGGCGCGCCGACTCGGACCTGCTGACCGTCTACAACGCGTACCTGGCC
TGGAAGCGGGTGTGCCGGTCGTCGGGCGGCGGCGCGGGCGGCCGCGAGTTCCAGTTCTGCCGCAAGAACTTCCTC
AGCCCGCAGACGCTGGCCGGCATCGAGGAGCTCAAGGGCCAGCTGCTGGCCTCGCTCGCCGACTCGGGCTTCCTG
CAGCTGACGGAGGAGGAGCGGCGGGCGCTCAAGGGCCAGCGCTCGGGCGGCGGGCGCGGGCGGCGGCAGCAGGCC
TTCTTCGAGGTGCCGCGGCGCGTCGACGGCAACAGCGACAACGACGCGGTCGCGGCCTCGGTCGTCGCCTGGAGC
TTCTACCCGAAGCTGCTGGTGCGCGACGCGCCGGGCGCCCGCGGCCTGCGCAACGTCGGCAACAACCAGTCCATC
AGCCTGCACCCGTCGTCCGTCAACCGCGGCCACCTCGACATCAAGTGGCTGGCCTACTACCACATCATGCAGTCC
AAGTCCGTCTACCACGCGCACGAGACGACGGCCGTCGAGCCCTTCGCCGTCGCCCTCCTCTGCGGCGACGTCCGC
TGCGACATGTTCTCGGGCGTCATCGTCCTCGACGGCAACCGCGCCCGCTTCGCCCTGCCGGACTGGAAGTCGATG
CTGGTGCTCAAGACGCTGCGCGCGCGCCTGCGCGAGCTGCTGGCCCGCGCCTTTCGCCAGCCCGGCAGGCTGGCC
ACGGCCCAGCACGAGAAGTGGCTCGACGTCTGGCAGCGCCTCTTCGCCGCGCCCGAGCCGCCCTCGGGGGCCGCG
GCCAAGCCTTAG
Transcript >Hirsu2|738
ATGGCCGGCACGAAGAAGAAGAAGAAGCCTGCCGTCAACCCGGCCCGGGGCTTCGCGACGACCTCGATCGCCTCC
AAGCCCAGGCCCGAGACGGAGCCCCAGCCGTCGCCGACCGCCCAAAAATCCAACGACGGCGATGCCCCTCCCTCG
TCGGCCGAGGACAGCGCCAGTGCCCCGCCGGCGGCCCAGCAGCAAGCTGGCGAAACGCCGCTGAGCCCCGAGGAG
TTCGAGAGGCGGCTCGAGGAGGCCGAGCTGCAGCTACTGGTCGAGAAGCACGCCCAGAAGGCCAAGCGCGACGCC
CAGCGCCAGCGCCAGCGCCTCGAGACGGACCGCCGCTTGCTGCGCAACCAGGCCGACACCGTCAACATCCCCAAG
TGGCTGCCCCCGGACCTGCTCGACCAGATCCTCGACCTGATAAAGGCCGAGACTCGCTTCTCTGCTTCGAGCGTC
TCGTCGGAAAATGCCGGGAGCGGCAGGATGCCCTCGGAGGAGGACATGATTCTCCGGCTGTGGACCCTGCGCCAA
ACTCTCGAGGCTGCTGCCTTCCCCGGCGAGAGAGTCGAGGCTGCGCTTCAGCACATCCTTGACATCGCTCCTCAC
GTGTCCACTGCCGTCAAGGACTCCATCTGGGGCCTGGACGAGGCCCTGGACTGGCTGGCGCGCCAATGCTCCCTT
GAGGAACTGCCGGCGTACGAGTCGCGCCCCAAGCCAGTCGCCAGAGATACGCCGACCGAAAGTCCGTTCTCGTCC
CGCCCGCATACGCCCAAGCCTCAAGATCCGCAGAGTAGTCGCGGGAATAAGGAATCAAGCAACGGCAACGGGCGC
GCCGCCAAGACGCCGTCCAAAAAGACGGCTGTGACTTTCGACGCCGACATCGAACCGGAGGACCTGATTCCCGAA
TACATCGCCGCCAAGGCAAAGCTTCTCGAGCTGAACCGTGCTCACGCTATGGGGAAGACCAGGCGCCATGACGCC
GGCAACGACGACACCGACGTGGAAATAGCAAAGCAGGAGGCCAAGCTGAGAAAAATCGACGGTGACGTGCTCTTC
GACAAATTCACAGCCGAGCAGCGCTGGAAGGTTGAGAGGGTGGCTGTGGAGAAAAAACTGGCGGCTGCGAGACAG
CACGCCCAGCAGGACCAAGAGCCCGGGGCATCGGATCCAGCCGCCGAGGCCGGAAAACCGGACGACGACGACATA
TCGGCCGAGGCGGAGCGCATCGCAGCCGAGGTCTTGGCCGACCAAGACGAAGACGACGATGATATTGCCGGTCTC
TTCGCGTCCCTGCCCCAGGACGAGGTTGACCCCCAGACCGGCAAGACACGAACCGTCATCAACTCCTCCAGCGGC
GCAAAGGTCGTGATACGGGACTTTGGCGATTGGACGGGTATCAAGCCTAGGAGGGTGCTGGAGGAGGCGTGTCGC
TCAAGGGATGCTTCCGTCAAAATCCACTACAGCACGGTGTCGGAGGCGACATTCGCGAATCGCCAGTCAATCGAC
ATCGGGTGGGCAAAGCCGCAGGAACCGCCCCAAAGTGAGCCCGGATCAGATGTGGAAATCGTTGCTGACCAAAAC
CGATTCACGTTCACGATGGTCGGGATCGCCACACCAGATGCTAAGCAGTCGGAAGCGTACATAGCCACCTCGGCT
CTCTTCCACATCTTCAGCGGCAATGCGAGGGAAGAAAAGGTCGGCCTGCGGTTGCCGCCTGTGTGGCGCGATTTA
TGGAACGAGTTGGCCGAGGCCAAGCAGAGTCGGCTGGACTCGATCGATCGCGACGTCGTCAAGTCCCTGAGGGCC
CTGGTCAGGCAGAGGCATGATCAGGAACTCGAAGATGGCGTCATCCTCCAAGGTGCCTTCCGAGGCCGGGGCACT
CCGAAAGCACATCAAGACGCAGCGGACAGCAGCCTGAGCGATCGCAAAAAGCAGAACTCGGCCAGCGGCGACGAG
TACAAAAAGATATGGGCCGACAAATCCGGCTCGCACAAATTTCAGACGATGCTGGAATCGAGGGCCCAGCTGCCC
ATGTGGCAGTTTCGGCCTCAAGTGCTCGATGCCGTAGACAAGAACCAGGTGGTCATCATCTGCGGCGAAACGGGA
TGTGGAAAGAGTACGCAAGTGCCGTCATTCCTGCTGGAGCACGAGCTCAGCCAAGGCAAAGCCTGCAAGATCTAC
TGCACGGAGCCGCGGCGTATCTCGGCCATATCGCTGGCCCGGCGAGTGAGCGAGGAGCTGGGCGAGAAGAAGGGC
GACCTGGGCACCAGCCGATCTCTCGTGGGCTACTCGATCCGCCTCGAGGCCAATACGACTCGCGAGACACGGCTG
GTGTACGCGACGACGGGTATCGTGATGCGCATGCTCGAAGGCTCCAACGACCTCCGCGAGGTGACGCATCTGGTG
CTCGACGAGGTGCACGAGCGGTCCATCGACAGCGACTTCCTCCTCATCGTCCTCAAGCGCCTGTTGGCGCAACGC
AAGGACCTCAAGGTGGTGCTCATGTCGGCCACGGTCGATGCCGAGCGCTTCTCGAGGTATCTCGGCCGGGCGCCG
ATCCTCAACGTGCCGGGACGGACGTTCCCCGTGGACGTGCGCTACCTCGAAGACGCCATCGAGGCGACCGGCTAC
AGCCCGACCAACTCGCCGGCCGACAAGATGATCGACCTGGACGACGACGCGATGGAGGAGGATGCCGGCAACGCG
AAGAGCGACGCGCCGCAGAGCCTATCCGCATATTCGGCCAAGACGCGCAGCGCGCTGTCGCAGATGGACGAGTAC
CAGATCGACTTCGACCTGGTCGTCCAGCTGATAGCCCACGTGGCCACAAGCGAGTCGCTGCAGCAGTACAGCAAG
GCAACGTTGGTCTTCCTGCCCGGCATCGCCGAGATCCGAACGCTGAACGACATGCTGCTCGGGGACCCGCGCTTC
GCAAAGGACTGCCTGGTGTATCCGCTGCATTCCACCATCGCGACCGAGGACCAGGAGTCGGCCTTCCTCGTGCCG
CCGCCCGGGACGCGCAAGATCGTGCTGGCGACCAACATAGCGGAAACGGGCATCACGATCCCGGACGTGACGTGC
GTCATCGACACGGGGAAGCACCGCGAGATGCGGTACGACGAGCGGAGGCAGCTGTCGAGGCTCATCGACACCTTC
ATCTCCCGGGCCAACGCGAAGCAGAGGCGGGGCCGTGCCGGGCGCGTGCAGAACGGCCTCTGCTTCCACCTGTTC
ACGCGGCACCGGCACGACAACCTGATGGCGGACCAGCAGACGCCGGAGATGCTGCGGCTGTCGCTGCAGGACCTC
GCGATCCGGGTCAAGATATGCAAAATCGGCGGCATCGAGGAGACGCTGGGGGACGCGCTGGACCCGCCGTCGGCC
AAGAACATACGGCGGGCGATCGACGCGCTCGTCGACGTGCGGGCGCTGACGATGGCGGAGGAGCTGACGCCGCTG
GGCCACCAGCTGGCGCGGCTGCCGCTCGACGTCTTCCTCGGCAAGCTGATCCTGCTCGGGACCGTCTTCAAGTGC
CTGGACATGGCGCTGACGGCGGCGGCGATCCTGTCGTCCAAGTCGCCCTTCTCGGCGCCCTTCGGGCAGCGGGCG
CAGGCCAACAACGCGCGCATGGCCTTCCGGCGCGCCGACTCGGACCTGCTGACCGTCTACAACGCGTACCTGGCC
TGGAAGCGGGTGTGCCGGTCGTCGGGCGGCGGCGCGGGCGGCCGCGAGTTCCAGTTCTGCCGCAAGAACTTCCTC
AGCCCGCAGACGCTGGCCGGCATCGAGGAGCTCAAGGGCCAGCTGCTGGCCTCGCTCGCCGACTCGGGCTTCCTG
CAGCTGACGGAGGAGGAGCGGCGGGCGCTCAAGGGCCAGCGCTCGGGCGGCGGGCGCGGGCGGCGGCAGCAGGCC
TTCTTCGAGGTGCCGCGGCGCGTCGACGGCAACAGCGACAACGACGCGGTCGCGGCCTCGGTCGTCGCCTGGAGC
TTCTACCCGAAGCTGCTGGTGCGCGACGCGCCGGGCGCCCGCGGCCTGCGCAACGTCGGCAACAACCAGTCCATC
AGCCTGCACCCGTCGTCCGTCAACCGCGGCCACCTCGACATCAAGTGGCTGGCCTACTACCACATCATGCAGTCC
AAGTCCGTCTACCACGCGCACGAGACGACGGCCGTCGAGCCCTTCGCCGTCGCCCTCCTCTGCGGCGACGTCCGC
TGCGACATGTTCTCGGGCGTCATCGTCCTCGACGGCAACCGCGCCCGCTTCGCCCTGCCGGACTGGAAGTCGATG
CTGGTGCTCAAGACGCTGCGCGCGCGCCTGCGCGAGCTGCTGGCCCGCGCCTTTCGCCAGCCCGGCAGGCTGGCC
ACGGCCCAGCACGAGAAGTGGCTCGACGTCTGGCAGCGCCTCTTCGCCGCGCCCGAGCCGCCCTCGGGGGCCGCG
GCCAAGCCTTAG
Gene >Hirsu2|738
ATGGCCGGCACGAAGAAGAAGAAGAAGCCTGCCGTCAACCCGGCCCGGGGCTTCGCGACGACCTCGATCGCCTCC
AAGCCCAGGCCCGAGACGGAGCCCCAGCCGTCGCCGACCGCCCAAAAATCCAACGACGGCGATGCCCCTCCCTCG
TCGGCCGAGGACAGCGCCAGTGCCCCGCCGGCGGCCCAGCAGCAAGCTGGCGAAACGCCGCTGAGCCCCGAGGAG
TTCGAGAGGCGGCTCGAGGAGGCCGAGCTGCAGCTACTGGTCGAGAAGCACGCCCAGAAGGCCAAGCGCGACGCC
CAGCGCCAGCGCCAGCGCCTCGAGACGGACCGCCGCTTGCTGCGCAACCAGGCCGACACCGTCAACATCCCCAAG
TGGCTGCCCCCGGACCTGCTCGACCAGATCCTCGACCTGATAAAGGCCGAGACTCGCTTCTCTGCTTCGAGCGTC
TCGTCGGAAAATGCCGGGAGCGGCAGGATGCCCTCGGAGGAGGACATGATTCTCCGGCTGTGGACCCTGCGCCAA
ACTCTCGAGGCTGCTGCCTTCCCCGGCGAGAGAGTCGAGGCTGCGCTTCAGCACATCCTTGACATCGCTCCTCAC
GTGTCCACTGCCGTCAAGGACTCCATCTGGGGCCTGGACGAGGCCCTGGACTGGCTGGCGCGCCAATGCTCCCTT
GAGGAACTGCCGGCGTACGAGTCGCGCCCCAAGCCAGTCGCCAGAGGTAAAGTCTTGACGGATCCATTCCGTCCC
TTGCCGGGCCTGACGCACTTACTCAGATTGCCTCCAGATACGCCGACCGAAAGTCCGTTCTCGTCCCGCCCGCAT
ACGCCCAAGCCTCAAGATCCGCAGAGTAGTCGCGGGAATAAGGAATCAAGCAACGGCAACGGGCGCGCCGCCAAG
ACGCCGTCCAAAAAGACGGCTGTGACTTTCGACGCCGACATCGAACCGGAGGACCTGATTCCCGAATACATCGCC
GCCAAGGCAAAGCTTCTCGAGCTGAACCGTGCTCACGCTATGGGGAAGACCAGGCGCCATGACGCCGGCAACGAC
GACACCGACGTGGAAATAGCAAAGCAGGAGGCCAAGCTGAGAAAAATCGACGGTGACGTGCTCTTCGACAAATTC
ACAGCCGAGCAGCGCTGGAAGGTTGAGAGGGTGGCTGTGGAGAAAAAACTGGCGGCTGCGAGACAGCACGCCCAG
CAGGACCAAGAGCCCGGGGCATCGGATCCAGCCGCCGAGGCCGGAAAACCGGACGACGACGACATATCGGCCGAG
GCGGAGCGCATCGCAGCCGAGGTCTTGGCCGACCAAGACGAAGACGACGATGATATTGCCGGTCTCTTCGCGTCC
CTGCCCCAGGACGAGGTTGACCCCCAGACCGGCAAGACACGAACCGTCATCAACTCCTCCAGCGGCGCAAAGGTC
GTGATACGGGACTTTGGCGATTGGACGGGTATCAAGCCTAGGAGGGTGCTGGAGGAGGCGTGTCGCTCAAGGCAA
GTAGCAGCCTCGGCCGCAGCACGAGTAACAGGGCATGGTCTGACCAGACTACAGGGATGCTTCCGTCAAAATCCA
CTACAGCACGGTGTCGGAGGCGACATTCGCGAATCGCCAGTCAATCGACATCGGGTGGGCAAAGCCGCAGGAACC
GCCCCAAAGTGAGCCCGGATCAGATGTGGAAATCGTTGCTGACCAAAACCGATTCACGTTCACGATGGTCGGGAT
CGCCACACCAGATGCTAAGCAGTCGGAAGCGTACATAGCCACCTCGGCTCTCTTCCACATCTTCAGCGGCAATGC
GAGGGAAGAAAAGGTCGGCCTGCGGTTGCCGCCTGTGTGGCGCGATTTATGGAACGAGTTGGCCGAGGCCAAGCA
GAGTCGGCTGGACTCGATCGATCGCGACGTCGTCAAGTCCCTGAGGGCCCTGGTCAGGCAGAGGCATGATCAGGA
ACTCGAAGATGGCGTCATCCTCCAAGGTGCCTTCCGAGGCCGGGGCACTCCGAAAGCACATCAAGACGCAGCGGA
CAGCAGCCTGAGCGATCGCAAAAAGCAGAACTCGGCCAGCGGCGACGAGTACAAAAAGATATGGGCCGACAAATC
CGGCTCGCACAAATTTCAGACGATGCTGGTAAGGCTGACCCAGACTCGTGGAGAATTGGCGGCTGACCAGCTCGA
CAGGAATCGAGGGCCCAGCTGCCCATGTGGCAGTTTCGGCCTCAAGTGCTCGATGCCGTAGACAAGAACCAGGTG
GTCATCATCTGCGGCGAAACGGGATGGTAAGTCGCGGCCGGTCGCGAGCCCTGAGTCTGACGATGTCTGACCTGC
CGCAGTGGAAAGAGTACGCAAGTGCCGTCATTCCTGCTGGAGCACGAGCTCAGCCAAGGCAAAGCCTGCAAGATC
TACTGCACGGAGCCGCGGCGTATCTCGGCCATATCGCTGGCCCGGCGAGTGAGCGAGGAGCTGGGCGAGAAGAAG
GGCGACCTGGGCACCAGCCGATCTCTCGTGGGCTACTCGATCCGCCTCGAGGCCAATACGACTCGCGAGACACGG
CTGGTGTACGCGACGACGGGTATCGTGATGCGCATGCTCGAAGGCTCCAACGACCTCCGCGAGGTGACGCATCTG
GTGCTCGACGAGGTGCACGAGCGGTCCATCGACAGCGACTTCCTCCTCATCGTCCTCAAGCGCCTGTTGGCGCAA
CGCAAGGACCTCAAGGTGGTGCTCATGTCGGCCACGGTCGATGCCGAGCGCTTCTCGAGGTATCTCGGCCGGGCG
CCGATCCTCAACGTGCCGGGACGGACGTTCCCCGTGGACGTGCGCTACCTCGAAGACGCCATCGAGGCGACCGGC
TACAGCCCGACCAACTCGCCGGCCGACAAGATGATCGACCTGGACGACGACGCGATGGAGGAGGATGCCGGCAAC
GCGAAGAGCGACGCGCCGCAGAGCCTATCCGCATATTCGGCCAAGACGCGCAGCGCGCTGTCGCAGATGGACGAG
TACCAGATCGACTTCGACCTGGTCGTCCAGCTGATAGCCCACGTGGCCACAAGCGAGTCGCTGCAGCAGTACAGC
AAGGCAACGTTGGTCTTCCTGCCCGGCATCGCCGAGATCCGAACGCTGAACGACATGCTGCTCGGGGACCCGCGC
TTCGCAAAGGACTGCCTGGTGTATCCGCTGCATTCCACCATCGCGACCGAGGACCAGGAGTCGGCCTTCCTCGTG
CCGCCGCCCGGGACGCGCAAGATCGTGCTGGCGACCAACATAGCGGAAACGGGCATCACGATCCCGGACGTGACG
TGCGTCATCGACACGGGGAAGCACCGCGAGATGCGGTACGACGAGCGGAGGCAGCTGTCGAGGCTCATCGACACC
TTCATCTCCCGGGCCAACGCGAAGCAGAGGCGGGGCCGTGCCGGGCGCGTGCAGAACGGCCTCTGCTTCCACCTG
TTCACGCGGCACCGGCACGACAACCTGATGGCGGACCAGCAGACGCCGGAGATGCTGCGGCTGTCGCTGCAGGAC
CTCGCGATCCGGGTCAAGATATGCAAAATCGGCGGCATCGAGGAGACGCTGGGGGACGCGCTGGACCCGCCGTCG
GCCAAGAACATACGGCGGGCGATCGACGCGCTCGTCGACGTGCGGGCGCTGACGATGGCGGAGGAGCTGACGCCG
CTGGGCCACCAGCTGGCGCGGCTGCCGCTCGACGTCTTCCTCGGCAAGCTGATCCTGCTCGGGACCGTCTTCAAG
TGCCTGGACATGGCGCTGACGGCGGCGGCGATCCTGTCGTCCAAGTCGCCCTTCTCGGCGCCCTTCGGGCAGCGG
GCGCAGGCCAACAACGCGCGCATGGCCTTCCGGCGCGCCGACTCGGACCTGCTGACCGTCTACAACGCGTACCTG
GCCTGGAAGCGGGTGTGCCGGTCGTCGGGCGGCGGCGCGGGCGGCCGCGAGTTCCAGTTCTGCCGCAAGAACTTC
CTCAGCCCGCAGACGCTGGCCGGCATCGAGGAGCTCAAGGGCCAGCTGCTGGCCTCGCTCGCCGACTCGGGCTTC
CTGCAGCTGACGGAGGAGGAGCGGCGGGCGCTCAAGGGCCAGCGCTCGGGCGGCGGGCGCGGGCGGCGGCAGCAG
GCCTTCTTCGAGGTGCCGCGGCGCGTCGACGGCAACAGCGACAACGACGCGGTCGCGGCCTCGGTCGTCGCCTGG
AGCTTCTACCCGAAGCTGCTGGTGCGCGACGCGCCGGGCGCCCGCGGCCTGCGCAACGTCGGCAACAACCAGTCC
ATCAGCCTGCACCCGTCGTCCGTCAACCGCGGCCACCTCGACATCAAGTGGCTGGCCTACTACCACATCATGCAG
TCCAAGTCGTGAGTTCCCGGCCCGGCCCCCCCGTCCCCCGGATCCCCGCCGCTGACCGGCGCCATATCCAGCGTC
TACCACGCGCACGAGACGACGGCCGTCGAGCCCTTCGCCGTCGCCCTCCTCTGCGGCGACGTCCGCTGCGACGTA
AGTCCCCCTCCCCCTCCTCTCCTCGCGTCCGGGGCTGACCGCCGCGCCTCGTCCCAGATGTTCTCGGGCGTCATC
GTCCTCGACGGCAACCGCGCCCGCTTCGCCCTGCCGGACTGGAAGTCGATGCTGGTGCTCAAGACGCTGCGCGCG
CGCCTGCGCGAGCTGCTGGCCCGCGCCTTTCGCCAGCCCGGCAGGCTGGCCACGGCCCAGCACGAGAAGTGGCTC
GACGTCTGGCAGCGCCTCTTCGCCGCGCCCGAGCCGCCCTCGGGGGCCGCGGCCAAGCCTTAG

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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