Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|2692
Gene name
Locationscaffold_218:11898..14826
Strand+
Gene length (bp)2928
Transcript length (bp)2760
Coding sequence length (bp)2757
Protein length (aa) 919

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00613 PI3Ka Phosphoinositide 3-kinase family, accessory domain (PIK domain) 7.8E-58 369 542
PF00454 PI3_PI4_kinase Phosphatidylinositol 3- and 4-kinase 1.6E-42 661 864
PF00792 PI3K_C2 Phosphoinositide 3-kinase C2 1.3E-32 58 221

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|P22543|VPS34_YEAST Phosphatidylinositol 3-kinase VPS34 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VPS34 PE=1 SV=1 7 919 0.0E+00
sp|P42347|PI3K1_SOYBN Phosphatidylinositol 3-kinase, root isoform OS=Glycine max PE=2 SV=1 8 918 0.0E+00
sp|P42348|PI3K2_SOYBN Phosphatidylinositol 3-kinase, nodule isoform OS=Glycine max PE=2 SV=1 8 918 0.0E+00
sp|Q5D891|PK3C3_PIG Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Sus scrofa GN=PIK3C3 PE=2 SV=1 5 918 0.0E+00
sp|P42339|PI3K_ARATH Phosphatidylinositol 3-kinase VPS34 OS=Arabidopsis thaliana GN=At1g60490 PE=2 SV=2 8 918 0.0E+00
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Swissprot ID Swissprot Description Start End E-value
sp|P22543|VPS34_YEAST Phosphatidylinositol 3-kinase VPS34 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VPS34 PE=1 SV=1 7 919 0.0E+00
sp|P42347|PI3K1_SOYBN Phosphatidylinositol 3-kinase, root isoform OS=Glycine max PE=2 SV=1 8 918 0.0E+00
sp|P42348|PI3K2_SOYBN Phosphatidylinositol 3-kinase, nodule isoform OS=Glycine max PE=2 SV=1 8 918 0.0E+00
sp|Q5D891|PK3C3_PIG Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Sus scrofa GN=PIK3C3 PE=2 SV=1 5 918 0.0E+00
sp|P42339|PI3K_ARATH Phosphatidylinositol 3-kinase VPS34 OS=Arabidopsis thaliana GN=At1g60490 PE=2 SV=2 8 918 0.0E+00
sp|P50520|VPS34_SCHPO Phosphatidylinositol 3-kinase vps34 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vps34 PE=2 SV=2 347 919 0.0E+00
sp|Q6AZN6|PK3C3_XENLA Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Xenopus laevis GN=pik3c3 PE=2 SV=1 5 918 0.0E+00
sp|Q6PF93|PK3C3_MOUSE Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Mus musculus GN=Pik3c3 PE=1 SV=1 335 918 4.0E-180
sp|O88763|PK3C3_RAT Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Rattus norvegicus GN=Pik3c3 PE=1 SV=1 335 918 3.0E-179
sp|Q8NEB9|PK3C3_HUMAN Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Homo sapiens GN=PIK3C3 PE=1 SV=1 335 918 3.0E-179
sp|P54676|PI3K4_DICDI Phosphatidylinositol 3-kinase VPS34-like OS=Dictyostelium discoideum GN=pikE PE=3 SV=2 10 919 6.0E-178
sp|Q92213|VPS34_CANAX Phosphatidylinositol 3-kinase VPS34 OS=Candida albicans GN=VPS34 PE=3 SV=1 11 919 8.0E-171
sp|P54675|PI3K3_DICDI Phosphatidylinositol 3-kinase 3 OS=Dictyostelium discoideum GN=pikC PE=2 SV=2 379 901 2.0E-74
sp|O35904|PK3CD_MOUSE Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform OS=Mus musculus GN=Pik3cd PE=1 SV=2 338 891 2.0E-73
sp|O00329|PK3CD_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform OS=Homo sapiens GN=PIK3CD PE=1 SV=2 393 891 4.0E-73
sp|P54673|PI3K1_DICDI Phosphatidylinositol 3-kinase 1 OS=Dictyostelium discoideum GN=pikA PE=2 SV=2 376 916 4.0E-72
sp|O02697|PK3CG_PIG Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Sus scrofa GN=PIK3CG PE=1 SV=2 373 896 6.0E-68
sp|P48736|PK3CG_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Homo sapiens GN=PIK3CG PE=1 SV=3 373 896 2.0E-67
sp|P54674|PI3K2_DICDI Phosphatidylinositol 3-kinase 2 OS=Dictyostelium discoideum GN=pikB PE=2 SV=2 381 915 2.0E-67
sp|Q9JHG7|PK3CG_MOUSE Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Mus musculus GN=Pik3cg PE=1 SV=2 373 896 8.0E-67
sp|O00443|P3C2A_HUMAN Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Homo sapiens GN=PIK3C2A PE=1 SV=2 393 915 2.0E-63
sp|Q5RAY1|P3C2A_PONAB Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Pongo abelii GN=PIK3C2A PE=2 SV=1 393 915 7.0E-63
sp|Q8BTI9|PK3CB_MOUSE Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Mus musculus GN=Pik3cb PE=1 SV=2 381 899 2.0E-62
sp|P32871|PK3CA_BOVIN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Bos taurus GN=PIK3CA PE=1 SV=1 368 891 2.0E-62
sp|Q61194|P3C2A_MOUSE Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Mus musculus GN=Pik3c2a PE=1 SV=2 393 915 4.0E-62
sp|Q9Z1L0|PK3CB_RAT Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Rattus norvegicus GN=Pik3cb PE=2 SV=1 381 899 4.0E-62
sp|P42336|PK3CA_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Homo sapiens GN=PIK3CA PE=1 SV=2 368 891 4.0E-62
sp|P42337|PK3CA_MOUSE Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Mus musculus GN=Pik3ca PE=1 SV=2 368 891 6.0E-62
sp|P42338|PK3CB_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Homo sapiens GN=PIK3CB PE=1 SV=1 381 899 3.0E-61
sp|O00750|P3C2B_HUMAN Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta OS=Homo sapiens GN=PIK3C2B PE=1 SV=2 380 915 1.0E-56
sp|O70173|P3C2G_RAT Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Rattus norvegicus GN=Pik3c2g PE=2 SV=1 389 915 2.0E-55
sp|O70167|P3C2G_MOUSE Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Mus musculus GN=Pik3c2g PE=2 SV=1 392 915 3.0E-55
sp|O75747|P3C2G_HUMAN Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Homo sapiens GN=PIK3C2G PE=1 SV=3 392 915 3.0E-53
sp|Q94125|AGE1_CAEEL Phosphatidylinositol 3-kinase age-1 OS=Caenorhabditis elegans GN=age-1 PE=1 SV=6 383 896 8.0E-47
sp|P0C5E7|AGE1_CAEBR Phosphatidylinositol 3-kinase age-1 OS=Caenorhabditis briggsae GN=age-1 PE=3 SV=1 382 841 1.0E-41
sp|Q8SQY7|STT4_ENCCU Probable phosphatidylinositol 4-kinase STT4 homolog OS=Encephalitozoon cuniculi (strain GB-M1) GN=STT4 PE=3 SV=2 443 887 4.0E-37
sp|Q8NEB9|PK3C3_HUMAN Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Homo sapiens GN=PIK3C3 PE=1 SV=1 5 251 1.0E-35
sp|Q6PF93|PK3C3_MOUSE Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Mus musculus GN=Pik3c3 PE=1 SV=1 5 251 2.0E-35
sp|O88763|PK3C3_RAT Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Rattus norvegicus GN=Pik3c3 PE=1 SV=1 5 251 6.0E-35
sp|P54677|PI4K_DICDI Phosphatidylinositol 4-kinase OS=Dictyostelium discoideum GN=pikD PE=3 SV=3 661 917 3.0E-33
sp|Q9SXA1|P4KA1_ARATH Phosphatidylinositol 4-kinase alpha 1 OS=Arabidopsis thaliana GN=PI4KA1 PE=1 SV=2 396 887 2.0E-30
sp|Q49GP3|PI4KB_DANRE Phosphatidylinositol 4-kinase beta OS=Danio rerio GN=pi4kb PE=2 SV=2 663 908 1.0E-29
sp|A4IID4|PI4KB_XENTR Phosphatidylinositol 4-kinase beta OS=Xenopus tropicalis GN=pi4kb PE=2 SV=1 663 908 3.0E-29
sp|O08561|PI4KB_RAT Phosphatidylinositol 4-kinase beta OS=Rattus norvegicus GN=Pi4kb PE=1 SV=1 663 908 7.0E-29
sp|Q8BKC8|PI4KB_MOUSE Phosphatidylinositol 4-kinase beta OS=Mus musculus GN=Pi4kb PE=1 SV=2 663 908 7.0E-29
sp|B2KI64|PI4KB_RHIFE Phosphatidylinositol 4-kinase beta OS=Rhinolophus ferrumequinum GN=PI4KB PE=3 SV=1 663 908 8.0E-29
sp|A9X1A0|PI4KB_PAPAN Phosphatidylinositol 4-kinase beta OS=Papio anubis GN=PI4KB PE=3 SV=2 663 908 8.0E-29
sp|Q9UBF8|PI4KB_HUMAN Phosphatidylinositol 4-kinase beta OS=Homo sapiens GN=PI4KB PE=1 SV=1 663 908 8.0E-29
sp|B1MTG7|PI4KB_CALMO Phosphatidylinositol 4-kinase beta OS=Callicebus moloch GN=PI4KB PE=3 SV=1 663 908 8.0E-29
sp|B0KWC1|PI4KB_CALJA Phosphatidylinositol 4-kinase beta OS=Callithrix jacchus GN=PI4KB PE=3 SV=1 663 908 9.0E-29
sp|B4UT09|PI4KB_OTOGA Phosphatidylinositol 4-kinase beta OS=Otolemur garnettii GN=PI4KB PE=3 SV=1 663 908 9.0E-29
sp|B3EX61|PI4KB_SORAR Phosphatidylinositol 4-kinase beta OS=Sorex araneus GN=PI4KB PE=3 SV=1 663 908 9.0E-29
sp|Q6GN16|PI4KB_XENLA Phosphatidylinositol 4-kinase beta OS=Xenopus laevis GN=pi4kb PE=2 SV=1 663 908 4.0E-28
sp|O08662|PI4KA_RAT Phosphatidylinositol 4-kinase alpha OS=Rattus norvegicus GN=Pi4ka PE=1 SV=1 428 899 5.0E-28
sp|O02810|PI4KB_BOVIN Phosphatidylinositol 4-kinase beta OS=Bos taurus GN=PI4KB PE=1 SV=2 663 908 6.0E-28
sp|Q5UR69|YL615_MIMIV Putative phosphatidylinositol kinase L615 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_L615 PE=3 SV=1 384 853 8.0E-28
sp|P42356|PI4KA_HUMAN Phosphatidylinositol 4-kinase alpha OS=Homo sapiens GN=PI4KA PE=1 SV=3 428 899 1.0E-27
sp|O02811|PI4KA_BOVIN Phosphatidylinositol 4-kinase alpha OS=Bos taurus GN=PI4KA PE=2 SV=1 428 899 3.0E-27
sp|Q9USR3|STT4_SCHPO Phosphatidylinositol 4-kinase stt4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=stt4 PE=3 SV=1 458 896 3.0E-27
sp|P37297|STT4_YEAST Phosphatidylinositol 4-kinase STT4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=STT4 PE=1 SV=1 414 895 9.0E-27
sp|Q9FMJ0|P4KB1_ARATH Phosphatidylinositol 4-kinase beta 1 OS=Arabidopsis thaliana GN=PI4KB1 PE=1 SV=1 663 887 2.0E-26
sp|Q0WPX9|P4KB2_ARATH Phosphatidylinositol 4-kinase beta 2 OS=Arabidopsis thaliana GN=PI4KB2 PE=2 SV=1 663 887 2.0E-25
sp|P39104|PIK1_YEAST Phosphatidylinositol 4-kinase PIK1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PIK1 PE=1 SV=1 663 917 2.0E-25
sp|Q8SR56|VPS34_ENCCU Probable phosphatidylinositol 3-kinase VPS34 homolog OS=Encephalitozoon cuniculi (strain GB-M1) GN=VPS34 PE=3 SV=2 625 918 4.0E-23
sp|Q9C680|P4KA2_ARATH Phosphatidylinositol 4-kinase alpha 2 OS=Arabidopsis thaliana GN=PI4KA2 PE=1 SV=1 621 894 5.0E-21
sp|Q9UW20|PIK1_CANAL Phosphatidylinositol 4-kinase PIK1alpha OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKALPHA PE=3 SV=1 663 855 3.0E-20
sp|Q9UW24|PIK1A_CANAL Phosphatidylinositol 4-kinase PIK1a OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKA PE=3 SV=1 663 855 2.0E-19
sp|A4QPH2|PI4P2_HUMAN Putative phosphatidylinositol 4-kinase alpha-like protein P2 OS=Homo sapiens GN=PI4KAP2 PE=5 SV=3 664 899 2.0E-19
sp|Q54ER4|ATR1_DICDI Probable serine/threonine-protein kinase atr1 OS=Dictyostelium discoideum GN=atr1 PE=3 SV=1 619 857 2.0E-11
sp|Q59LR2|ATR_CANAL Serine/threonine-protein kinase MEC1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=MEC1 PE=3 SV=1 637 888 7.0E-10
sp|Q10366|PIK1_SCHPO Phosphatidylinositol 4-kinase pik1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=pik1 PE=1 SV=1 663 855 1.0E-08
sp|Q75DB8|ATR_ASHGO Serine/threonine-protein kinase MEC1 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=MEC1 PE=3 SV=3 641 857 6.0E-07
sp|Q6CT34|ATR_KLULA Serine/threonine-protein kinase MEC1 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=MEC1 PE=3 SV=1 632 825 4.0E-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 - 46 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|2692
MTDYGRMDPFSFAGSKDVDHPVSIRIMNLDGEEPPVKYSTLLDRPDLRHVGSNTSPFSDLYVTVQVWAGSKALTV
PVQTAYKSFRSERKWNEWLELPITYKQLPVNARLAITIWDLSPTGGKHALDHSIPFGGTTLPMFDADNQVQKGRQ
KCLVHRHRHADGTDNSQTPALLVPRKTPGSRAGKVPCLDKDAEELDRMEKLFKKHEMGEIQRVDWLDQMVFRSFE
KRGLQAAKSSMKMLQRQRAVNGDGVEADDDDAQAEDHGRSSPSAFLLNVELPRFDFPVVFADHEYDPPPISSLQP
LSASQGSISQRQPQVHFGPGINGLGESSDGFGTRLIKVYDPEVGQRDNPAEAKHRRLFRSSHRHGILDKDLKPNA
KVRDELNLIMSYSPTHILSPEETDLVWKFRYHLTRDKRALTKFVKSVNWNDQSEAKQAIQVLGSWTEIDVDDALE
LLGPSFDNPAVRSYAVDRLRKADDAELLLYLLQLVQALKYEHISTESDHDGAQDSSLASFLIQRAAANFMLGNYL
YWYLMVECDDHSPEQGLDNRNIYRKVAYEFMTQLVRQPDGAENRKTLLRQAELVAIISKIAGEVKVSNESIAKKA
DRVKAFLADAKNELVTLDPPLAMPLDPSIKIIGVAADQVTVFKSSLNPIKITFKTTTGSAYPIIFKLGDDLRQDQ
LVIQIITLMDQLLRKENLDLKLSPYKILATSTTAGASQFVQSQSLSSIVGKFKTNPALAYLRHHNPDDRQPLGVR
QETLDTYIKSCAGYCVITYILGVGDRHLDNLLLAPDGHFFHADFGFILGRDPKPFAPVMKLSKEMVECMGGVQSE
HYQRFRQYCFLAYTALRKSSNLILNLFSLMVHANIPDIRLEPDKAVIKVRERFHLELSEEEAIVYFGNVIDGTLT
AFAPVVIDKLHEWAQALRA
Coding >Ophio5|2692
ATGACCGACTACGGGAGGATGGACCCCTTCTCCTTTGCGGGGTCCAAGGACGTGGACCATCCCGTCAGCATCCGC
ATAATGAACCTGGACGGCGAAGAACCTCCTGTCAAGTACTCGACACTTCTCGACCGGCCTGACCTCCGACATGTC
GGTTCAAATACAAGTCCTTTCTCCGATCTCTACGTCACCGTCCAAGTCTGGGCCGGCTCGAAAGCCCTTACTGTA
CCTGTACAGACTGCTTACAAGTCGTTTCGATCGGAAAGAAAATGGAACGAGTGGCTCGAGCTTCCCATCACCTAC
AAGCAGCTACCGGTCAACGCCCGCCTGGCTATCACAATCTGGGACTTGTCGCCGACCGGAGGCAAGCATGCGCTC
GACCATTCCATTCCCTTTGGGGGCACCACCTTGCCCATGTTTGATGCAGACAACCAAGTGCAAAAGGGACGTCAG
AAATGCCTCGTGCACAGGCACAGACATGCCGACGGAACCGACAACTCCCAGACGCCAGCCCTGCTCGTGCCGAGA
AAGACGCCGGGGTCAAGGGCTGGCAAAGTGCCATGTCTCGACAAGGACGCCGAGGAACTCGATAGAATGGAGAAG
CTCTTCAAGAAGCACGAGATGGGGGAGATACAGCGCGTCGACTGGCTGGATCAGATGGTCTTTCGCAGCTTCGAG
AAACGTGGACTTCAGGCCGCCAAGTCCTCTATGAAGATGCTCCAGCGCCAGCGCGCTGTCAACGGCGACGGCGTG
GAAGCGGACGACGACGACGCCCAAGCTGAAGACCATGGACGCTCCAGCCCGTCTGCCTTTCTTCTCAACGTCGAG
CTACCGCGTTTCGACTTTCCCGTCGTCTTTGCAGACCACGAATACGACCCGCCGCCGATATCGTCCCTGCAGCCT
CTCTCGGCCTCCCAAGGAAGCATCTCTCAGCGACAGCCCCAAGTTCACTTCGGCCCGGGCATCAACGGCTTAGGG
GAAAGCTCCGACGGCTTCGGGACGCGACTCATCAAGGTCTACGACCCCGAGGTGGGTCAGAGGGACAACCCGGCT
GAGGCCAAGCACAGAAGACTCTTCCGAAGCTCTCACCGACATGGCATTCTAGATAAAGACCTGAAGCCGAATGCA
AAGGTCCGCGACGAACTGAACCTGATCATGTCGTACTCGCCTACGCACATACTATCGCCCGAGGAGACGGACCTG
GTCTGGAAGTTTCGCTATCACCTTACTCGTGACAAGAGGGCGTTGACCAAGTTCGTAAAGTCGGTTAACTGGAAT
GACCAGAGTGAAGCCAAGCAGGCGATACAGGTCCTCGGGAGCTGGACCGAGATCGACGTGGACGATGCCCTCGAG
CTTCTCGGCCCTTCCTTTGACAACCCGGCCGTCCGGTCGTACGCCGTCGATAGGCTGCGCAAGGCCGACGACGCC
GAACTGCTACTGTACTTGCTGCAGCTGGTTCAGGCACTCAAGTACGAGCACATCTCGACGGAGTCGGATCATGAC
GGCGCGCAGGACTCGTCCCTGGCCAGCTTCCTGATCCAGCGGGCGGCCGCCAACTTCATGCTCGGCAACTATCTG
TACTGGTACCTCATGGTGGAATGCGACGACCACAGCCCGGAGCAGGGCCTCGACAACCGCAACATCTACCGCAAG
GTTGCGTACGAGTTCATGACGCAGCTTGTCCGGCAGCCGGACGGGGCGGAAAACAGGAAGACCCTACTGCGACAG
GCCGAGCTGGTGGCCATCATTTCCAAGATAGCGGGCGAGGTTAAGGTGTCTAACGAGTCCATCGCCAAAAAGGCC
GATCGCGTCAAGGCGTTCCTGGCAGATGCCAAGAACGAGCTGGTGACGTTGGATCCGCCGCTTGCGATGCCGTTG
GATCCGTCCATCAAGATCATAGGCGTGGCGGCTGACCAGGTGACGGTCTTCAAGTCGTCGCTGAACCCCATCAAA
ATCACCTTCAAGACGACGACGGGCAGCGCCTATCCCATCATCTTCAAGTTGGGCGACGACCTGCGACAGGACCAG
CTGGTGATACAGATCATCACGCTCATGGACCAGCTGCTGCGCAAAGAGAACCTGGATCTGAAGCTATCGCCGTAC
AAGATCCTTGCGACGAGCACGACGGCTGGTGCGTCTCAGTTTGTGCAGTCGCAGAGCCTGTCGAGCATCGTGGGC
AAGTTCAAGACCAATCCGGCACTGGCCTACCTGCGTCACCACAACCCGGACGACAGGCAGCCGCTCGGGGTGCGG
CAAGAGACGCTCGACACGTACATCAAGTCGTGTGCCGGCTACTGCGTCATCACCTACATCCTCGGCGTCGGCGAC
CGTCACCTCGACAACCTGCTCCTCGCGCCGGACGGGCACTTCTTCCACGCCGACTTTGGCTTCATCCTCGGGCGC
GATCCCAAGCCGTTTGCGCCGGTGATGAAGCTCTCCAAGGAGATGGTCGAGTGCATGGGCGGCGTCCAGTCGGAG
CACTATCAGCGGTTCCGCCAGTACTGCTTCCTCGCCTACACGGCGCTGCGCAAGTCGTCCAACCTCATCCTCAAC
CTCTTCAGCCTCATGGTACACGCCAACATTCCCGACATCCGCCTCGAGCCGGACAAGGCCGTCATCAAGGTCCGC
GAGCGCTTCCACCTCGAACTTAGCGAGGAGGAGGCCATCGTCTACTTTGGTAACGTCATCGATGGCACCCTGACG
GCCTTTGCGCCCGTCGTCATTGACAAGTTGCACGAGTGGGCGCAGGCGTTGCGGGCA
Transcript >Ophio5|2692
ATGACCGACTACGGGAGGATGGACCCCTTCTCCTTTGCGGGGTCCAAGGACGTGGACCATCCCGTCAGCATCCGC
ATAATGAACCTGGACGGCGAAGAACCTCCTGTCAAGTACTCGACACTTCTCGACCGGCCTGACCTCCGACATGTC
GGTTCAAATACAAGTCCTTTCTCCGATCTCTACGTCACCGTCCAAGTCTGGGCCGGCTCGAAAGCCCTTACTGTA
CCTGTACAGACTGCTTACAAGTCGTTTCGATCGGAAAGAAAATGGAACGAGTGGCTCGAGCTTCCCATCACCTAC
AAGCAGCTACCGGTCAACGCCCGCCTGGCTATCACAATCTGGGACTTGTCGCCGACCGGAGGCAAGCATGCGCTC
GACCATTCCATTCCCTTTGGGGGCACCACCTTGCCCATGTTTGATGCAGACAACCAAGTGCAAAAGGGACGTCAG
AAATGCCTCGTGCACAGGCACAGACATGCCGACGGAACCGACAACTCCCAGACGCCAGCCCTGCTCGTGCCGAGA
AAGACGCCGGGGTCAAGGGCTGGCAAAGTGCCATGTCTCGACAAGGACGCCGAGGAACTCGATAGAATGGAGAAG
CTCTTCAAGAAGCACGAGATGGGGGAGATACAGCGCGTCGACTGGCTGGATCAGATGGTCTTTCGCAGCTTCGAG
AAACGTGGACTTCAGGCCGCCAAGTCCTCTATGAAGATGCTCCAGCGCCAGCGCGCTGTCAACGGCGACGGCGTG
GAAGCGGACGACGACGACGCCCAAGCTGAAGACCATGGACGCTCCAGCCCGTCTGCCTTTCTTCTCAACGTCGAG
CTACCGCGTTTCGACTTTCCCGTCGTCTTTGCAGACCACGAATACGACCCGCCGCCGATATCGTCCCTGCAGCCT
CTCTCGGCCTCCCAAGGAAGCATCTCTCAGCGACAGCCCCAAGTTCACTTCGGCCCGGGCATCAACGGCTTAGGG
GAAAGCTCCGACGGCTTCGGGACGCGACTCATCAAGGTCTACGACCCCGAGGTGGGTCAGAGGGACAACCCGGCT
GAGGCCAAGCACAGAAGACTCTTCCGAAGCTCTCACCGACATGGCATTCTAGATAAAGACCTGAAGCCGAATGCA
AAGGTCCGCGACGAACTGAACCTGATCATGTCGTACTCGCCTACGCACATACTATCGCCCGAGGAGACGGACCTG
GTCTGGAAGTTTCGCTATCACCTTACTCGTGACAAGAGGGCGTTGACCAAGTTCGTAAAGTCGGTTAACTGGAAT
GACCAGAGTGAAGCCAAGCAGGCGATACAGGTCCTCGGGAGCTGGACCGAGATCGACGTGGACGATGCCCTCGAG
CTTCTCGGCCCTTCCTTTGACAACCCGGCCGTCCGGTCGTACGCCGTCGATAGGCTGCGCAAGGCCGACGACGCC
GAACTGCTACTGTACTTGCTGCAGCTGGTTCAGGCACTCAAGTACGAGCACATCTCGACGGAGTCGGATCATGAC
GGCGCGCAGGACTCGTCCCTGGCCAGCTTCCTGATCCAGCGGGCGGCCGCCAACTTCATGCTCGGCAACTATCTG
TACTGGTACCTCATGGTGGAATGCGACGACCACAGCCCGGAGCAGGGCCTCGACAACCGCAACATCTACCGCAAG
GTTGCGTACGAGTTCATGACGCAGCTTGTCCGGCAGCCGGACGGGGCGGAAAACAGGAAGACCCTACTGCGACAG
GCCGAGCTGGTGGCCATCATTTCCAAGATAGCGGGCGAGGTTAAGGTGTCTAACGAGTCCATCGCCAAAAAGGCC
GATCGCGTCAAGGCGTTCCTGGCAGATGCCAAGAACGAGCTGGTGACGTTGGATCCGCCGCTTGCGATGCCGTTG
GATCCGTCCATCAAGATCATAGGCGTGGCGGCTGACCAGGTGACGGTCTTCAAGTCGTCGCTGAACCCCATCAAA
ATCACCTTCAAGACGACGACGGGCAGCGCCTATCCCATCATCTTCAAGTTGGGCGACGACCTGCGACAGGACCAG
CTGGTGATACAGATCATCACGCTCATGGACCAGCTGCTGCGCAAAGAGAACCTGGATCTGAAGCTATCGCCGTAC
AAGATCCTTGCGACGAGCACGACGGCTGGTGCGTCTCAGTTTGTGCAGTCGCAGAGCCTGTCGAGCATCGTGGGC
AAGTTCAAGACCAATCCGGCACTGGCCTACCTGCGTCACCACAACCCGGACGACAGGCAGCCGCTCGGGGTGCGG
CAAGAGACGCTCGACACGTACATCAAGTCGTGTGCCGGCTACTGCGTCATCACCTACATCCTCGGCGTCGGCGAC
CGTCACCTCGACAACCTGCTCCTCGCGCCGGACGGGCACTTCTTCCACGCCGACTTTGGCTTCATCCTCGGGCGC
GATCCCAAGCCGTTTGCGCCGGTGATGAAGCTCTCCAAGGAGATGGTCGAGTGCATGGGCGGCGTCCAGTCGGAG
CACTATCAGCGGTTCCGCCAGTACTGCTTCCTCGCCTACACGGCGCTGCGCAAGTCGTCCAACCTCATCCTCAAC
CTCTTCAGCCTCATGGTACACGCCAACATTCCCGACATCCGCCTCGAGCCGGACAAGGCCGTCATCAAGGTCCGC
GAGCGCTTCCACCTCGAACTTAGCGAGGAGGAGGCCATCGTCTACTTTGGTAACGTCATCGATGGCACCCTGACG
GCCTTTGCGCCCGTCGTCATTGACAAGTTGCACGAGTGGGCGCAGGCGTTGCGGGCATGA
Gene >Ophio5|2692
ATGACCGACTACGGGAGGATGGACCCCTTCTCCTTTGCGGGGTCCAAGGACGTGGACCATCCCGTCAGCATCCGC
ATGTGAGCCTCTTCCACCCGCCGTCTGCTTGCCCTACTAACGCTCTTCTGTCCGCAGAATGAACCTGGACGGCGA
AGAACCTCCTGTCAAGTACTCGACACTTCTCGACCGGCCTGACCTCCGACATGTCGGTTCAAATACAAGGTGGGA
GTTGTCCAGGTGCCGCCAGTAGACACGAGAGTTGATGAGCGCTGTGCAGTCCTTTCTCCGATCTCTACGTCACCG
TCCAAGTCTGGGCCGGCTCGAAAGCCCTTACTGTACCTGTACAGACTGCTTACAAGTCGTTTCGATCGGAAAGAA
AGTATGTCGACACGCCCGCCGTCCCAAGATGAGTCTGCGCATACTGATGCTTGCAAAAGATGGAACGAGTGGCTC
GAGCTTCCCATCACCTACAAGCAGCTACCGGTCAACGCCCGCCTGGCTATCACAATCTGGGACTTGTCGCCGACC
GGAGGCAAGCATGCGCTCGACCATTCCATTCCCTTTGGGGGCACCACCTTGCCCATGTTTGATGCAGACAACCAA
GTGCAAAAGGGACGTCAGAAATGCCTCGTGCACAGGCACAGACATGCCGACGGAACCGACAACTCCCAGACGCCA
GCCCTGCTCGTGCCGAGAAAGACGCCGGGGTCAAGGGCTGGCAAAGTGCCATGTCTCGACAAGGACGCCGAGGAA
CTCGATAGAATGGAGAAGCTCTTCAAGAAGCACGAGATGGGGGAGATACAGCGCGTCGACTGGCTGGATCAGATG
GTCTTTCGCAGCTTCGAGAAACGTGGACTTCAGGCCGCCAAGTCCTCTATGAAGATGCTCCAGCGCCAGCGCGCT
GTCAACGGCGACGGCGTGGAAGCGGACGACGACGACGCCCAAGCTGAAGACCATGGACGCTCCAGCCCGTCTGCC
TTTCTTCTCAACGTCGAGCTACCGCGTTTCGACTTTCCCGTCGTCTTTGCAGACCACGAATACGACCCGCCGCCG
ATATCGTCCCTGCAGCCTCTCTCGGCCTCCCAAGGAAGCATCTCTCAGCGACAGCCCCAAGTTCACTTCGGCCCG
GGCATCAACGGCTTAGGGGAAAGCTCCGACGGCTTCGGGACGCGACTCATCAAGGTCTACGACCCCGAGGTGGGT
CAGAGGGACAACCCGGCTGAGGCCAAGCACAGAAGACTCTTCCGAAGCTCTCACCGACATGGCATTCTAGATAAA
GACCTGAAGCCGAATGCAAAGGTCCGCGACGAACTGAACCTGATCATGTCGTACTCGCCTACGCACATACTATCG
CCCGAGGAGACGGACCTGGTCTGGAAGTTTCGCTATCACCTTACTCGTGACAAGAGGGCGTTGACCAAGTTCGTA
AAGTCGGTTAACTGGAATGACCAGAGTGAAGCCAAGCAGGCGATACAGGTCCTCGGGAGCTGGACCGAGATCGAC
GTGGACGATGCCCTCGAGCTTCTCGGCCCTTCCTTTGACAACCCGGCCGTCCGGTCGTACGCCGTCGATAGGCTG
CGCAAGGCCGACGACGCCGAACTGCTACTGTACTTGCTGCAGCTGGTTCAGGCACTCAAGTACGAGCACATCTCG
ACGGAGTCGGATCATGACGGCGCGCAGGACTCGTCCCTGGCCAGCTTCCTGATCCAGCGGGCGGCCGCCAACTTC
ATGCTCGGCAACTATCTGTACTGGTACCTCATGGTGGAATGCGACGACCACAGCCCGGAGCAGGGCCTCGACAAC
CGCAACATCTACCGCAAGGTTGCGTACGAGTTCATGACGCAGCTTGTCCGGCAGCCGGACGGGGCGGAAAACAGG
AAGACCCTACTGCGACAGGCCGAGCTGGTGGCCATCATTTCCAAGATAGCGGGCGAGGTTAAGGTGTCTAACGAG
TCCATCGCCAAAAAGGCCGATCGCGTCAAGGCGTTCCTGGCAGATGCCAAGAACGAGCTGGTGACGTTGGATCCG
CCGCTTGCGATGCCGTTGGATCCGTCCATCAAGATCATAGGCGTGGCGGCTGACCAGGTGACGGTCTTCAAGTCG
TCGCTGAACCCCATCAAAATCACCTTCAAGACGACGACGGGCAGCGCCTATCCCATCATCTTCAAGTTGGGCGAC
GACCTGCGACAGGACCAGCTGGTGATACAGATCATCACGCTCATGGACCAGCTGCTGCGCAAAGAGAACCTGGAT
CTGAAGCTATCGCCGTACAAGATCCTTGCGACGAGCACGACGGCTGGTGCGTCTCAGTTTGTGCAGTCGCAGAGC
CTGTCGAGCATCGTGGGCAAGTTCAAGACCAATCCGGCACTGGCCTACCTGCGTCACCACAACCCGGACGACAGG
CAGCCGCTCGGGGTGCGGCAAGAGACGCTCGACACGTACATCAAGTCGTGTGCCGGCTACTGCGTCATCACCTAC
ATCCTCGGCGTCGGCGACCGTCACCTCGACAACCTGCTCCTCGCGCCGGACGGGCACTTCTTCCACGCCGACTTT
GGCTTCATCCTCGGGCGCGATCCCAAGCCGTTTGCGCCGGTGATGAAGCTCTCCAAGGAGATGGTCGAGTGCATG
GGCGGCGTCCAGTCGGAGCACTATCAGCGGTTCCGCCAGTACTGCTTCCTCGCCTACACGGCGCTGCGCAAGTCG
TCCAACCTCATCCTCAACCTCTTCAGCCTCATGGTACACGCCAACATTCCCGACATCCGCCTCGAGCCGGACAAG
GCCGTCATCAAGGTCCGCGAGCGCTTCCACCTCGAACTTAGCGAGGAGGAGGCCATCGTCTACTTTGGTAACGTC
ATCGATGGCACCCTGACGGCCTTTGCGCCCGTCGTCATTGACAAGTTGCACGAGTGGGCGCAGGCGTTGCGGGCA
TGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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