Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|1972
Gene name
Locationscaffold_178:20372..22498
Strand-
Gene length (bp)2126
Transcript length (bp)1899
Coding sequence length (bp)1896
Protein length (aa) 632

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF01485 IBR IBR domain, a half RING-finger domain 5.4E-12 316 382
PF01485 IBR IBR domain, a half RING-finger domain 2.2E-08 400 445
PF19422 Ariadne Ariadne domain 3.5E-13 467 585

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q9P3U4|HEL1_SCHPO E3 ubiquitin-protein ligase dbl4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=dbl4 PE=3 SV=1 112 622 0.0E+00
sp|Q94981|ARI1_DROME Protein ariadne-1 OS=Drosophila melanogaster GN=ari-1 PE=1 SV=2 167 618 1.0E-130
sp|Q9Y4X5|ARI1_HUMAN E3 ubiquitin-protein ligase ARIH1 OS=Homo sapiens GN=ARIH1 PE=1 SV=2 167 621 8.0E-124
sp|Q9Z1K5|ARI1_MOUSE E3 ubiquitin-protein ligase ARIH1 OS=Mus musculus GN=Arih1 PE=1 SV=3 167 621 1.0E-123
sp|B1H1E4|ARI1_XENTR E3 ubiquitin-protein ligase arih1 OS=Xenopus tropicalis GN=arih1 PE=2 SV=1 105 621 1.0E-123
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Swissprot ID Swissprot Description Start End E-value
sp|Q9P3U4|HEL1_SCHPO E3 ubiquitin-protein ligase dbl4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=dbl4 PE=3 SV=1 112 622 0.0E+00
sp|Q94981|ARI1_DROME Protein ariadne-1 OS=Drosophila melanogaster GN=ari-1 PE=1 SV=2 167 618 1.0E-130
sp|Q9Y4X5|ARI1_HUMAN E3 ubiquitin-protein ligase ARIH1 OS=Homo sapiens GN=ARIH1 PE=1 SV=2 167 621 8.0E-124
sp|Q9Z1K5|ARI1_MOUSE E3 ubiquitin-protein ligase ARIH1 OS=Mus musculus GN=Arih1 PE=1 SV=3 167 621 1.0E-123
sp|B1H1E4|ARI1_XENTR E3 ubiquitin-protein ligase arih1 OS=Xenopus tropicalis GN=arih1 PE=2 SV=1 105 621 1.0E-123
sp|A2VEA3|ARI1_BOVIN E3 ubiquitin-protein ligase ARIH1 OS=Bos taurus GN=ARIH1 PE=2 SV=1 167 621 1.0E-123
sp|Q6NW85|ARI1L_DANRE E3 ubiquitin-protein ligase arih1l OS=Danio rerio GN=arih1l PE=2 SV=1 167 621 5.0E-123
sp|Q6PFJ9|ARI1_DANRE E3 ubiquitin-protein ligase arih1 OS=Danio rerio GN=arih1 PE=2 SV=1 167 621 1.0E-122
sp|Q32NS4|ARI1_XENLA E3 ubiquitin-protein ligase arih1 OS=Xenopus laevis GN=arih1 PE=2 SV=1 167 621 2.0E-122
sp|Q6T486|RBRA_DICDI Probable E3 ubiquitin-protein ligase rbrA OS=Dictyostelium discoideum GN=rbrA PE=3 SV=1 117 612 9.0E-99
sp|P36113|HEL1_YEAST E3 ubiquitin-protein ligase HEL2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HEL1 PE=1 SV=1 166 605 2.0E-90
sp|O76924|ARI2_DROME Protein ariadne-2 OS=Drosophila melanogaster GN=ari-2 PE=2 SV=1 105 606 6.0E-85
sp|Q9Z1K6|ARI2_MOUSE E3 ubiquitin-protein ligase ARIH2 OS=Mus musculus GN=Arih2 PE=1 SV=1 180 609 2.0E-83
sp|O95376|ARI2_HUMAN E3 ubiquitin-protein ligase ARIH2 OS=Homo sapiens GN=ARIH2 PE=1 SV=1 181 609 2.0E-82
sp|Q84RR0|ARI7_ARATH Probable E3 ubiquitin-protein ligase ARI7 OS=Arabidopsis thaliana GN=ARI7 PE=2 SV=1 105 580 2.0E-79
sp|Q8L829|ARI5_ARATH Probable E3 ubiquitin-protein ligase ARI5 OS=Arabidopsis thaliana GN=ARI5 PE=2 SV=1 132 582 5.0E-75
sp|Q22431|ARI2_CAEEL Probable protein ariadne-2 OS=Caenorhabditis elegans GN=T12E12.1 PE=3 SV=2 118 576 1.0E-71
sp|Q9LVX0|ARI3_ARATH Probable E3 ubiquitin-protein ligase ARI3 OS=Arabidopsis thaliana GN=ARI3 PE=2 SV=1 147 613 2.0E-71
sp|P0C8K8|ARI6_ARATH Putative E3 ubiquitin-protein ligase ARI6 OS=Arabidopsis thaliana GN=ARI6 PE=5 SV=1 166 578 3.0E-71
sp|Q9LVW9|ARI4_ARATH Putative E3 ubiquitin-protein ligase ARI4 OS=Arabidopsis thaliana GN=ARI4 PE=5 SV=2 118 616 2.0E-70
sp|Q84RR2|ARI2_ARATH Probable E3 ubiquitin-protein ligase ARI2 OS=Arabidopsis thaliana GN=ARI2 PE=2 SV=1 137 585 5.0E-70
sp|Q8W468|ARI8_ARATH Probable E3 ubiquitin-protein ligase ARI8 OS=Arabidopsis thaliana GN=ARI8 PE=2 SV=1 166 584 5.0E-70
sp|Q9SKC3|ARI9_ARATH Probable E3 ubiquitin-protein ligase ARI9 OS=Arabidopsis thaliana GN=ARI9 PE=2 SV=1 117 580 1.0E-66
sp|Q9SKC4|ARI10_ARATH Probable E3 ubiquitin-protein ligase ARI10 OS=Arabidopsis thaliana GN=ARI10 PE=2 SV=1 166 580 3.0E-65
sp|Q9P2G1|AKIB1_HUMAN Ankyrin repeat and IBR domain-containing protein 1 OS=Homo sapiens GN=ANKIB1 PE=1 SV=3 167 614 4.0E-65
sp|Q6ZPS6|AKIB1_MOUSE Ankyrin repeat and IBR domain-containing protein 1 OS=Mus musculus GN=Ankib1 PE=1 SV=2 167 614 2.0E-64
sp|Q949V6|ARI1_ARATH Probable E3 ubiquitin-protein ligase ARI1 OS=Arabidopsis thaliana GN=ARI1 PE=2 SV=1 162 598 7.0E-64
sp|Q9SKC2|ARI11_ARATH Probable E3 ubiquitin-protein ligase ARI11 OS=Arabidopsis thaliana GN=ARI11 PE=2 SV=1 116 546 1.0E-62
sp|Q1L8G6|AKIB1_DANRE Ankyrin repeat and IBR domain-containing protein 1 OS=Danio rerio GN=ankib1 PE=3 SV=1 174 632 1.0E-57
sp|Q8IWT3|CUL9_HUMAN Cullin-9 OS=Homo sapiens GN=CUL9 PE=1 SV=2 168 577 7.0E-36
sp|Q80TT8|CUL9_MOUSE Cullin-9 OS=Mus musculus GN=Cul9 PE=1 SV=2 168 577 2.0E-30
sp|Q9C5A4|ARI16_ARATH Probable E3 ubiquitin-protein ligase ARI16 OS=Arabidopsis thaliana GN=ARI16 PE=2 SV=1 167 580 3.0E-30
sp|Q84RQ9|ARI12_ARATH Probable E3 ubiquitin-protein ligase ARI12 OS=Arabidopsis thaliana GN=ARI12 PE=2 SV=2 142 614 1.0E-26
sp|Q9FFN9|ARI13_ARATH Probable E3 ubiquitin-protein ligase ARI13 OS=Arabidopsis thaliana GN=ARI13 PE=2 SV=1 167 579 5.0E-24
sp|Q54CX4|Y5521_DICDI Uncharacterized protein DDB_G0292642 OS=Dictyostelium discoideum GN=DDB_G0292642 PE=3 SV=2 246 457 2.0E-22
sp|Q9UBS8|RNF14_HUMAN E3 ubiquitin-protein ligase RNF14 OS=Homo sapiens GN=RNF14 PE=1 SV=1 244 440 2.0E-20
sp|Q9JI90|RNF14_MOUSE E3 ubiquitin-protein ligase RNF14 OS=Mus musculus GN=Rnf14 PE=1 SV=2 244 440 7.0E-20
sp|Q9FFP1|ARI14_ARATH Probable E3 ubiquitin-protein ligase ARI14 OS=Arabidopsis thaliana GN=ARI14 PE=2 SV=1 167 545 7.0E-19
sp|Q84RQ8|ARI15_ARATH Probable E3 ubiquitin-protein ligase ARI15 OS=Arabidopsis thaliana GN=ARI15 PE=2 SV=1 263 584 9.0E-18
sp|Q1L8L6|RN19B_DANRE E3 ubiquitin-protein ligase RNF19B OS=Danio rerio GN=rnf19b PE=3 SV=2 263 458 3.0E-17
sp|A2A7Q9|RN19B_MOUSE E3 ubiquitin-protein ligase RNF19B OS=Mus musculus GN=Rnf19b PE=1 SV=2 261 458 5.0E-17
sp|Q6ZMZ0|RN19B_HUMAN E3 ubiquitin-protein ligase RNF19B OS=Homo sapiens GN=RNF19B PE=1 SV=2 261 458 5.0E-17
sp|Q9US46|ITT1_SCHPO E3 ubiquitin-protein ligase itt1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=itt1 PE=3 SV=1 241 446 7.0E-17
sp|Q2VJ60|RN19A_PIG E3 ubiquitin-protein ligase RNF19A OS=Sus scrofa GN=RNF19A PE=2 SV=1 261 439 1.0E-16
sp|Q9NV58|RN19A_HUMAN E3 ubiquitin-protein ligase RNF19A OS=Homo sapiens GN=RNF19A PE=1 SV=3 261 439 1.0E-16
sp|P50636|RN19A_MOUSE E3 ubiquitin-protein ligase RNF19A OS=Mus musculus GN=Rnf19a PE=1 SV=2 261 439 1.0E-16
sp|Q8BKD6|R144B_MOUSE E3 ubiquitin-protein ligase RNF144B OS=Mus musculus GN=Rnf144b PE=2 SV=2 220 439 1.0E-15
sp|A5PK27|R144B_BOVIN E3 ubiquitin-protein ligase RNF144B OS=Bos taurus GN=RNF144B PE=2 SV=1 234 439 2.0E-15
sp|Q08B84|RN19B_XENLA E3 ubiquitin-protein ligase RNF19B OS=Xenopus laevis GN=rnf19b PE=2 SV=2 261 458 4.0E-15
sp|Q7Z419|R144B_HUMAN E3 ubiquitin-protein ligase RNF144B OS=Homo sapiens GN=RNF144B PE=1 SV=1 235 439 6.0E-15
sp|F4KGU4|DEAHC_ARATH ATP-dependent RNA helicase DEAH12, chloroplastic OS=Arabidopsis thaliana GN=At5g10370 PE=3 SV=1 246 444 3.0E-13
sp|Q5RFV4|R1441_DANRE Probable E3 ubiquitin-protein ligase RNF144A-A OS=Danio rerio GN=rnf144aa PE=3 SV=1 250 439 1.0E-12
sp|P0CE10|DEAHB_ARATH ATP-dependent RNA helicase DEAH11, chloroplastic OS=Arabidopsis thaliana GN=At4g01020 PE=3 SV=1 246 444 2.0E-11
sp|P50876|R144A_HUMAN E3 ubiquitin-protein ligase RNF144A OS=Homo sapiens GN=RNF144A PE=1 SV=2 262 439 2.0E-11
sp|Q925F3|R144A_MOUSE E3 ubiquitin-protein ligase RNF144A OS=Mus musculus GN=Rnf144a PE=1 SV=1 262 439 2.0E-11
sp|Q6DH94|R1442_DANRE Probable E3 ubiquitin-protein ligase RNF144A-B OS=Danio rerio GN=rnf144ab PE=2 SV=1 250 439 6.0E-11
sp|A4IIY1|R144A_XENTR Probable E3 ubiquitin-protein ligase RNF144A OS=Xenopus tropicalis GN=rnf144a PE=2 SV=1 262 439 1.0E-10
sp|Q8TC41|RN217_HUMAN Probable E3 ubiquitin-protein ligase RNF217 OS=Homo sapiens GN=RNF217 PE=2 SV=4 244 438 2.0E-08
sp|D3YYI7|RN217_MOUSE Probable E3 ubiquitin-protein ligase RNF217 OS=Mus musculus GN=Rnf217 PE=3 SV=2 244 438 6.0E-08
sp|Q4KLT0|RN217_XENLA Probable E3 ubiquitin-protein ligase RNF217 OS=Xenopus laevis GN=rnf217 PE=2 SV=1 253 438 7.0E-08
sp|Q9WVS6|PRKN2_MOUSE E3 ubiquitin-protein ligase parkin OS=Mus musculus GN=Park2 PE=1 SV=1 364 451 2.0E-07
sp|Q9JK66|PRKN2_RAT E3 ubiquitin-protein ligase parkin OS=Rattus norvegicus GN=Park2 PE=1 SV=1 364 451 5.0E-07
sp|Q96EP0|RNF31_HUMAN E3 ubiquitin-protein ligase RNF31 OS=Homo sapiens GN=RNF31 PE=1 SV=1 268 465 1.0E-06
sp|Q924T7|RNF31_MOUSE E3 ubiquitin-protein ligase RNF31 OS=Mus musculus GN=Rnf31 PE=1 SV=2 261 465 1.0E-06
sp|Q5UQ35|YR811_MIMIV Putative ariadne-like RING finger protein R811 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R811 PE=3 SV=1 390 465 4.0E-06
sp|O60260|PRKN2_HUMAN E3 ubiquitin-protein ligase parkin OS=Homo sapiens GN=PARK2 PE=1 SV=2 364 451 5.0E-06
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GO

(None)

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 64 0.45

Transmembrane Domains

(None)

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|1972
MALNDPRRFPEAPPPTTTLGHQGKKHAACDLVALPPDSIISGAAEATLSPLPCLFTRLPLAHSISIPPRRRPTLD
EPSLPDQGDECQVKRLVASAAPPTPVTTGMDSEEEYMSNMSSDDEIMQEYSGDEMSAGEDFDEEDFAEPDPDFGL
SPKDLDRAKRPSHATSFKVYQPDDIERQQHEMINEVNMILDMRKEDAAILLRHFRWNKERLLEDYMDRPDQVLEA
AGLRNNARAPPKLEAIPGFVCDICCEDEVGLESFALKCGHRYCVNCYRHYLTQKIRGEGEAARIQCPADGCGRIL
DSRSLDLLVTVDLTGRYHELLNRTYVEDKDIFKWCPAPDCPNVIECGVKKKDLDKVVPTVECRCGYRFCFGCPNA
DHQPAPCDLVKKWLKKCADDSETANWISANTKECPKCSSTIEKNGGCNHMTCRKCKYEFCWMCMGLWSEHGTSWY
NCNRYEEKSGAEARDAQARSRTSLERYLHYYNRYANHEQSAKLDKDIAQKTEKKMVQLQTTSGMSWIEVQYLNSA
SQVLQTCRQTLKWTYAFAFYLAKNNLTEIFEDNQKDLEMAVENLSEMFEKSIQELADPKLKVDIMDKTSYCKKRR
LILLEDTADNLAKAKWTFNSDLTNPGAAAPRR
Coding >Ophio5|1972
ATGGCCCTGAACGATCCACGCCGTTTCCCTGAAGCCCCCCCGCCAACAACAACTCTCGGTCACCAGGGGAAAAAA
CACGCAGCCTGTGACCTCGTCGCCCTGCCTCCTGACAGCATCATCTCCGGTGCAGCCGAGGCTACGTTGTCCCCT
TTGCCGTGCCTTTTTACTCGTCTGCCTCTCGCTCACTCTATCTCTATCCCTCCTCGTCGACGCCCAACCCTCGAC
GAGCCGAGTCTCCCCGACCAAGGGGACGAGTGCCAAGTCAAAAGGCTCGTCGCCTCAGCTGCCCCCCCGACACCC
GTCACCACCGGCATGGATTCGGAGGAGGAGTACATGTCCAACATGTCGAGCGACGACGAGATCATGCAGGAGTAC
AGTGGTGACGAGATGTCGGCAGGAGAAGACTTCGACGAGGAAGACTTCGCTGAGCCGGATCCCGATTTTGGTCTT
TCGCCCAAGGACCTGGACAGGGCGAAACGGCCTAGTCACGCCACTTCCTTCAAGGTGTACCAACCCGATGACATC
GAGCGCCAGCAGCACGAAATGATCAACGAGGTTAACATGATTCTCGACATGCGCAAGGAGGACGCGGCCATTCTT
CTCCGACACTTCCGGTGGAACAAGGAGCGCCTGCTCGAAGACTATATGGACCGTCCCGATCAGGTGCTCGAGGCT
GCCGGCCTGCGGAATAACGCCCGAGCGCCGCCCAAACTCGAGGCCATCCCCGGCTTCGTCTGTGACATTTGCTGC
GAGGATGAGGTCGGGCTCGAGTCTTTTGCTCTCAAGTGCGGTCATCGGTACTGCGTCAACTGCTACAGGCATTAC
CTGACACAAAAGATCCGCGGTGAAGGTGAGGCCGCTCGGATCCAGTGCCCGGCCGACGGCTGCGGCCGCATCCTC
GACTCCCGCTCCCTCGACCTGCTCGTGACGGTCGACCTGACGGGCCGCTATCACGAGCTTCTCAACCGTACCTAC
GTCGAGGACAAGGACATCTTCAAGTGGTGCCCGGCGCCCGACTGTCCCAACGTCATCGAGTGCGGCGTCAAGAAG
AAGGACCTGGACAAGGTGGTGCCCACGGTCGAATGTCGATGTGGCTACCGTTTCTGCTTCGGGTGCCCGAACGCG
GACCACCAACCAGCCCCGTGCGACCTGGTCAAGAAGTGGCTTAAGAAGTGTGCCGACGACTCCGAGACGGCCAAC
TGGATATCCGCCAACACCAAGGAGTGCCCCAAGTGCAGCTCGACGATTGAGAAGAATGGCGGCTGCAACCACATG
ACGTGCCGCAAATGTAAGTACGAGTTCTGCTGGATGTGCATGGGTCTCTGGTCGGAGCACGGCACCAGCTGGTAC
AACTGCAACCGATACGAGGAGAAGAGCGGCGCCGAGGCCCGCGATGCCCAAGCCCGATCCCGCACGTCGCTGGAG
CGCTACCTACACTATTACAACCGCTATGCGAACCACGAACAGTCGGCTAAGCTGGATAAGGACATTGCGCAGAAG
ACTGAAAAAAAGATGGTGCAGCTGCAGACGACATCGGGCATGTCGTGGATCGAGGTGCAATACCTCAACTCGGCG
TCGCAGGTATTACAGACGTGCCGTCAGACGCTTAAGTGGACCTACGCCTTTGCCTTTTACCTGGCCAAGAACAAC
TTGACGGAGATCTTCGAGGACAACCAAAAGGACCTCGAGATGGCGGTGGAGAACCTGTCGGAGATGTTCGAGAAG
TCGATCCAGGAGCTGGCCGACCCCAAGCTCAAGGTGGACATTATGGACAAGACGTCGTACTGCAAGAAGCGCAGG
CTCATCCTGCTCGAGGACACGGCCGACAACCTCGCCAAGGCTAAATGGACCTTCAACTCTGATCTGACCAACCCT
GGCGCGGCTGCACCTCGTCGC
Transcript >Ophio5|1972
ATGGCCCTGAACGATCCACGCCGTTTCCCTGAAGCCCCCCCGCCAACAACAACTCTCGGTCACCAGGGGAAAAAA
CACGCAGCCTGTGACCTCGTCGCCCTGCCTCCTGACAGCATCATCTCCGGTGCAGCCGAGGCTACGTTGTCCCCT
TTGCCGTGCCTTTTTACTCGTCTGCCTCTCGCTCACTCTATCTCTATCCCTCCTCGTCGACGCCCAACCCTCGAC
GAGCCGAGTCTCCCCGACCAAGGGGACGAGTGCCAAGTCAAAAGGCTCGTCGCCTCAGCTGCCCCCCCGACACCC
GTCACCACCGGCATGGATTCGGAGGAGGAGTACATGTCCAACATGTCGAGCGACGACGAGATCATGCAGGAGTAC
AGTGGTGACGAGATGTCGGCAGGAGAAGACTTCGACGAGGAAGACTTCGCTGAGCCGGATCCCGATTTTGGTCTT
TCGCCCAAGGACCTGGACAGGGCGAAACGGCCTAGTCACGCCACTTCCTTCAAGGTGTACCAACCCGATGACATC
GAGCGCCAGCAGCACGAAATGATCAACGAGGTTAACATGATTCTCGACATGCGCAAGGAGGACGCGGCCATTCTT
CTCCGACACTTCCGGTGGAACAAGGAGCGCCTGCTCGAAGACTATATGGACCGTCCCGATCAGGTGCTCGAGGCT
GCCGGCCTGCGGAATAACGCCCGAGCGCCGCCCAAACTCGAGGCCATCCCCGGCTTCGTCTGTGACATTTGCTGC
GAGGATGAGGTCGGGCTCGAGTCTTTTGCTCTCAAGTGCGGTCATCGGTACTGCGTCAACTGCTACAGGCATTAC
CTGACACAAAAGATCCGCGGTGAAGGTGAGGCCGCTCGGATCCAGTGCCCGGCCGACGGCTGCGGCCGCATCCTC
GACTCCCGCTCCCTCGACCTGCTCGTGACGGTCGACCTGACGGGCCGCTATCACGAGCTTCTCAACCGTACCTAC
GTCGAGGACAAGGACATCTTCAAGTGGTGCCCGGCGCCCGACTGTCCCAACGTCATCGAGTGCGGCGTCAAGAAG
AAGGACCTGGACAAGGTGGTGCCCACGGTCGAATGTCGATGTGGCTACCGTTTCTGCTTCGGGTGCCCGAACGCG
GACCACCAACCAGCCCCGTGCGACCTGGTCAAGAAGTGGCTTAAGAAGTGTGCCGACGACTCCGAGACGGCCAAC
TGGATATCCGCCAACACCAAGGAGTGCCCCAAGTGCAGCTCGACGATTGAGAAGAATGGCGGCTGCAACCACATG
ACGTGCCGCAAATGTAAGTACGAGTTCTGCTGGATGTGCATGGGTCTCTGGTCGGAGCACGGCACCAGCTGGTAC
AACTGCAACCGATACGAGGAGAAGAGCGGCGCCGAGGCCCGCGATGCCCAAGCCCGATCCCGCACGTCGCTGGAG
CGCTACCTACACTATTACAACCGCTATGCGAACCACGAACAGTCGGCTAAGCTGGATAAGGACATTGCGCAGAAG
ACTGAAAAAAAGATGGTGCAGCTGCAGACGACATCGGGCATGTCGTGGATCGAGGTGCAATACCTCAACTCGGCG
TCGCAGGTATTACAGACGTGCCGTCAGACGCTTAAGTGGACCTACGCCTTTGCCTTTTACCTGGCCAAGAACAAC
TTGACGGAGATCTTCGAGGACAACCAAAAGGACCTCGAGATGGCGGTGGAGAACCTGTCGGAGATGTTCGAGAAG
TCGATCCAGGAGCTGGCCGACCCCAAGCTCAAGGTGGACATTATGGACAAGACGTCGTACTGCAAGAAGCGCAGG
CTCATCCTGCTCGAGGACACGGCCGACAACCTCGCCAAGGCTAAATGGACCTTCAACTCTGATCTGACCAACCCT
GGCGCGGCTGCACCTCGTCGCTGA
Gene >Ophio5|1972
ATGGCCCTGAACGATCCACGCCGTTTCCCTGAAGCCCCCCCGCCAACAACAACTCTCGGTCACCAGGGGAAAAAA
CACGCAGCCTGTGACCTCGTCGCCCTGCCTCCTGACAGCATCATCTCCGGTGCAGCCGAGGCTACGTTGTCCCCT
TTGCCGTGCCTTTTTACTCGTCTGCCTCTCGCTCACTCTATCTCTATCCCTCGTCACCCGGTTTCAGGCCCCTCC
CCCCTTCTATCTCGTGTCAGCTCGTCGACGCCCAACCCTCGACGAGCCGAGTCTGTACCGTCACCATTCCCCCCT
TGCAGAGAAAGCGAAAGGCTGCTGAGGCGACGATTAGCCCCGACCAAGGGGACGAGTGCCAAGTCAAAAGGCTCG
TCGCCTCAGCTGCCCCCCCGACACCCGTCACCACCGGCATGGATTCGGAGGAGGAGTACATGTCCAACATGTCGA
GCGACGACGAGATCATGCAGGAGTACAGTGGTGACGAGATGTCGGCAGGAGAAGGTAAAGGTCGCCACCTCCCTC
TCCCGGCAATAGCTTCTGACAAAGCCCAGACTTCGACGAGGAAGACTTCGCTGAGCCGGATCCCGATTTTGGTCT
TTCGCCCAAGGACCTGGACAGGGCGAAACGGCCTAGTCACGCCACTTCCTTCAAGGTGTACCAACCCGATGACAT
CGAGCGCCAGCAGCACGAAATGATCAACGAGGTTAACATGATTCTCGACATGCGCAAGGAGGACGCGGCCATTCT
TCTCCGACACTTCCGGTGGAACAAGGAGCGCCTGCTCGAAGACTATATGGACCGTCCCGATCAGGTGCTCGAGGC
TGCCGGCCTGCGGAATAACGCCCGAGCGCCGCCCAAACTCGAGGCCATCCCCGGCTTCGTCTGTGACATTTGCTG
CGAGGATGAGGTCGGGCTCGAGTCTTTTGCTCTCAAGTGCGGTCATCGGTACTGCGTCAACTGCTACAGGCATTA
CCTGACACAAAAGATCCGCGGTGAAGGTGAGGCCGCTCGGATCCAGTGCCCGGCCGACGGCTGCGGCCGCATCCT
CGACTCCCGCTCCCTCGACCTGCTCGTGACGGTCGACCTGACGGGCCGCTATCACGAGCTTCTCAACCGTACCTA
CGTCGAGGACAAGGACATCTTCAAGTGGTGCCCGGCGCCCGACTGTCCCAACGTCATCGAGTGCGGCGTCAAGAA
GAAGGACCTGGACAAGGTGGTGCCCACGGTCGAATGTCGATGTGGCTACCGTTTCTGCTTCGGGTGCCCGAACGC
GGACCACCAACCAGCCCCGTGCGACCTGGTCAAGAAGTGGCTTAAGAAGTGTGCCGACGACTCCGAGACGGCCAA
CTGGATATCCGCCAACACCAAGGAGTGCCCCAAGTGCAGCTCGACGATTGAGAAGAATGGCGGCTGCAACCACAT
GACGTGCCGCAAATGTAAGTACGAGTTCTGCTGGATGTGCATGGGTCTCTGGTCGGAGCACGGCACCAGCTGGTA
CAACTGCAACCGATACGAGGAGAAGAGCGGCGCCGAGGCCCGCGATGCCCAAGCCCGATCCCGCACGTCGCTGGA
GCGCTACCTACACTATTACAACCGCTATGCGAACCACGAACAGTCGGCTAAGCTGGATAAGGACATTGCGCAGAA
GACTGAAAAAAAGATGGTGCAGCTGCAGACGACATCGGGCATGTCGTGGATCGAGGTGCAATACCTCAACTCGGC
GTCGCAGGTATTACAGACGTGCCGTCAGACGCTTAAGTGGACCTACGCCTTTGCCTTTTACCTGGCCAAGAACAA
CTTGACGGAGATCTTCGAGGACAACCAAAAGGACCTCGAGATGGCGGTGGAGAACCTGTCGGAGATGTTCGAGAA
GTCGATCCAGGAGCTGGCCGACCCCAAGCTCAAGGTGGACATTATGGACAAGACGTCGTACTGCAAGAAGCGCAG
GCTCATCCTGCTCGAGGACACGGCCGACAACCTCGCCAAGGGTAAGATGAGGCTCGAAATGCACGAAGAAGACGA
CACGGGCTGACAGCGATTTTTTTTTTCTCTCCCTTCCTTTAGCTAAATGGACCTTCAACTCTGATCTGACCAACC
CTGGCGCGGCTGCACCTCGTCGCTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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