Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauG2|5044
Gene name
LocationContig_445:10704..14738
Strand+
Gene length (bp)4034
Transcript length (bp)3855
Coding sequence length (bp)3855
Protein length (aa) 1285

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF02383 Syja_N SacI homology domain 1.9E-72 102 450
PF03372 Exo_endo_phos Endonuclease/Exonuclease/phosphatase family 3.3E-09 664 947

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|P50942|INP52_YEAST Polyphosphatidylinositol phosphatase INP52 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP52 PE=1 SV=1 23 1173 0.0E+00
sp|O43001|SYJ1_SCHPO Inositol-1,4,5-trisphosphate 5-phosphatase 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=syj1 PE=1 SV=1 23 1086 0.0E+00
sp|Q12271|INP53_YEAST Polyphosphatidylinositol phosphatase INP53 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP53 PE=1 SV=1 24 980 0.0E+00
sp|P40559|INP51_YEAST Phosphatidylinositol 4,5-bisphosphate 5-phosphatase INP51 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP51 PE=1 SV=1 103 1062 3.0E-156
sp|Q9USQ6|SYJ2_SCHPO Inositol-1,4,5-trisphosphate 5-phosphatase 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=syj2 PE=2 SV=1 76 958 2.0E-123
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Swissprot ID Swissprot Description Start End E-value
sp|P50942|INP52_YEAST Polyphosphatidylinositol phosphatase INP52 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP52 PE=1 SV=1 23 1173 0.0E+00
sp|O43001|SYJ1_SCHPO Inositol-1,4,5-trisphosphate 5-phosphatase 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=syj1 PE=1 SV=1 23 1086 0.0E+00
sp|Q12271|INP53_YEAST Polyphosphatidylinositol phosphatase INP53 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP53 PE=1 SV=1 24 980 0.0E+00
sp|P40559|INP51_YEAST Phosphatidylinositol 4,5-bisphosphate 5-phosphatase INP51 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP51 PE=1 SV=1 103 1062 3.0E-156
sp|Q9USQ6|SYJ2_SCHPO Inositol-1,4,5-trisphosphate 5-phosphatase 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=syj2 PE=2 SV=1 76 958 2.0E-123
sp|O15056|SYNJ2_HUMAN Synaptojanin-2 OS=Homo sapiens GN=SYNJ2 PE=1 SV=3 195 972 2.0E-113
sp|Q9D2G5|SYNJ2_MOUSE Synaptojanin-2 OS=Mus musculus GN=Synj2 PE=1 SV=2 195 972 5.0E-112
sp|O43426|SYNJ1_HUMAN Synaptojanin-1 OS=Homo sapiens GN=SYNJ1 PE=1 SV=2 183 972 7.0E-112
sp|Q62910|SYNJ1_RAT Synaptojanin-1 OS=Rattus norvegicus GN=Synj1 PE=1 SV=3 183 972 9.0E-112
sp|Q8CHC4|SYNJ1_MOUSE Synaptojanin-1 OS=Mus musculus GN=Synj1 PE=1 SV=3 183 972 1.0E-111
sp|O18964|SYNJ1_BOVIN Synaptojanin-1 (Fragment) OS=Bos taurus GN=SYNJ1 PE=1 SV=2 183 972 2.0E-110
sp|O55207|SYNJ2_RAT Synaptojanin-2 OS=Rattus norvegicus GN=Synj2 PE=1 SV=2 195 972 2.0E-109
sp|Q8K337|I5P2_MOUSE Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Mus musculus GN=Inpp5b PE=1 SV=1 642 972 1.0E-61
sp|P32019|I5P2_HUMAN Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Homo sapiens GN=INPP5B PE=1 SV=4 642 972 2.0E-61
sp|Q01968|OCRL_HUMAN Inositol polyphosphate 5-phosphatase OCRL-1 OS=Homo sapiens GN=OCRL PE=1 SV=3 646 973 4.0E-58
sp|Q6NVF0|OCRL_MOUSE Inositol polyphosphate 5-phosphatase OCRL-1 OS=Mus musculus GN=Ocrl PE=1 SV=1 646 972 2.0E-56
sp|D3ZGS3|OCRL_RAT Inositol polyphosphate 5-phosphatase OCRL-1 OS=Rattus norvegicus GN=Ocrl PE=1 SV=1 646 972 2.0E-56
sp|A1L244|SAC1A_DANRE Phosphatidylinositide phosphatase SAC1-A OS=Danio rerio GN=sacm1la PE=2 SV=1 195 624 2.0E-49
sp|Q9ES21|SAC1_RAT Phosphatidylinositide phosphatase SAC1 OS=Rattus norvegicus GN=Sacm1l PE=1 SV=1 97 624 3.0E-49
sp|Q9EP69|SAC1_MOUSE Phosphatidylinositide phosphatase SAC1 OS=Mus musculus GN=Sacm1l PE=1 SV=1 97 624 2.0E-48
sp|Q9NTJ5|SAC1_HUMAN Phosphatidylinositide phosphatase SAC1 OS=Homo sapiens GN=SACM1L PE=1 SV=2 97 624 3.0E-48
sp|Q5R921|SAC1_PONAB Phosphatidylinositide phosphatase SAC1 OS=Pongo abelii GN=SACM1L PE=2 SV=1 97 624 4.0E-48
sp|Q6GM29|SAC1_XENLA Phosphatidylinositide phosphatase SAC1 OS=Xenopus laevis GN=sacm1l PE=2 SV=1 99 624 4.0E-47
sp|P32368|SAC1_YEAST Phosphoinositide phosphatase SAC1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SAC1 PE=1 SV=1 199 624 1.0E-46
sp|Q0WT19|IP5P8_ARATH Type I inositol polyphosphate 5-phosphatase 8 OS=Arabidopsis thaliana GN=IP5P8 PE=2 SV=1 659 967 2.0E-46
sp|A6QL88|SAC1_BOVIN Phosphatidylinositide phosphatase SAC1 OS=Bos taurus GN=SACM1L PE=2 SV=1 97 624 2.0E-46
sp|Q55AW9|SAC1_DICDI Phosphatidylinositide phosphatase SAC1 OS=Dictyostelium discoideum GN=sac1 PE=3 SV=1 195 616 6.0E-46
sp|A4VCH0|SAC1B_DANRE Phosphatidylinositide phosphatase SAC1-B OS=Danio rerio GN=sacm1lb PE=2 SV=2 99 624 2.0E-45
sp|O14306|YE8A_SCHPO Probable inositol polyphosphate 5-phosphatase C9G1.10c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC9G1.10c PE=1 SV=2 638 1001 2.0E-44
sp|Q9SIS4|IP5P9_ARATH Type IV inositol polyphosphate 5-phosphatase 9 OS=Arabidopsis thaliana GN=IP5P9 PE=1 SV=1 693 960 3.0E-44
sp|Q9LR47|IP5P6_ARATH Type IV inositol polyphosphate 5-phosphatase 6 OS=Arabidopsis thaliana GN=IP5P6 PE=1 SV=2 741 981 2.0E-43
sp|Q66GQ6|IP5P5_ARATH Type I inositol polyphosphate 5-phosphatase 5 OS=Arabidopsis thaliana GN=IP5P5 PE=2 SV=1 738 960 3.0E-43
sp|Q0WQ41|IP5P7_ARATH Type IV inositol polyphosphate 5-phosphatase 7 OS=Arabidopsis thaliana GN=IP5P7 PE=1 SV=1 741 1002 4.0E-43
sp|A8E7C5|SAC2_DANRE Phosphatidylinositide phosphatase SAC2 OS=Danio rerio GN=inpp5f PE=3 SV=1 196 624 2.0E-42
sp|Q9W0I6|SAC1_DROME Phosphatidylinositide phosphatase SAC1 OS=Drosophila melanogaster GN=Sac1 PE=2 SV=1 84 627 7.0E-42
sp|Q8GTS0|IP5P4_ARATH Type I inositol polyphosphate 5-phosphatase 4 OS=Arabidopsis thaliana GN=IP5P4 PE=2 SV=1 733 973 2.0E-41
sp|Q9Y2H2|SAC2_HUMAN Phosphatidylinositide phosphatase SAC2 OS=Homo sapiens GN=INPP5F PE=1 SV=3 198 624 6.0E-41
sp|Q84MA2|IP5P1_ARATH Type I inositol polyphosphate 5-phosphatase 1 OS=Arabidopsis thaliana GN=IP5P1 PE=1 SV=2 708 961 8.0E-41
sp|A8MR21|IP5PA_ARATH Type I inositol polyphosphate 5-phosphatase 10 OS=Arabidopsis thaliana GN=IP5P10 PE=2 SV=1 740 962 3.0E-40
sp|Q8H0Z6|IP5P3_ARATH Type IV inositol polyphosphate 5-phosphatase 3 OS=Arabidopsis thaliana GN=IP5P3 PE=1 SV=1 742 1000 5.0E-40
sp|Q8CDA1|SAC2_MOUSE Phosphatidylinositide phosphatase SAC2 OS=Mus musculus GN=Inpp5f PE=1 SV=1 198 624 9.0E-40
sp|Q96328|SAC8_ARATH Phosphoinositide phosphatase SAC8 OS=Arabidopsis thaliana GN=SAC8 PE=2 SV=1 195 625 5.0E-39
sp|Q9JII1|INP5E_MOUSE 72 kDa inositol polyphosphate 5-phosphatase OS=Mus musculus GN=Inpp5e PE=1 SV=1 645 958 1.0E-38
sp|Q9C5G5|SAC7_ARATH Phosphoinositide phosphatase SAC7 OS=Arabidopsis thaliana GN=SAC7 PE=2 SV=1 298 627 2.0E-38
sp|A0FI79|INP5E_PANTR 72 kDa inositol polyphosphate 5-phosphatase OS=Pan troglodytes GN=INPP5E PE=2 SV=1 622 958 3.0E-38
sp|Q9WVR1|INP5E_RAT 72 kDa inositol polyphosphate 5-phosphatase OS=Rattus norvegicus GN=Inpp5e PE=1 SV=2 622 958 3.0E-38
sp|Q9NRR6|INP5E_HUMAN 72 kDa inositol polyphosphate 5-phosphatase OS=Homo sapiens GN=INPP5E PE=1 SV=2 622 958 3.0E-38
sp|O60162|YG23_SCHPO Uncharacterized protein C19F5.03 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC19F5.03 PE=1 SV=1 194 626 7.0E-38
sp|Q7X911|SAC6_ARATH Phosphoinositide phosphatase SAC6 OS=Arabidopsis thaliana GN=SAC6 PE=2 SV=1 250 627 1.0E-37
sp|Q9JMC1|PI5PA_RAT Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A OS=Rattus norvegicus GN=Inpp5j PE=1 SV=1 689 972 6.0E-36
sp|Q9FUR2|IP5P2_ARATH Type I inositol polyphosphate 5-phosphatase 2 OS=Arabidopsis thaliana GN=IP5P2 PE=1 SV=2 723 962 7.0E-36
sp|P59644|PI5PA_MOUSE Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A OS=Mus musculus GN=Inpp5j PE=1 SV=2 689 972 2.0E-35
sp|Q15735|PI5PA_HUMAN Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A OS=Homo sapiens GN=INPP5J PE=1 SV=3 738 972 2.0E-35
sp|Q84W55|IP5PF_ARATH Type II inositol polyphosphate 5-phosphatase 15 OS=Arabidopsis thaliana GN=IP5P15 PE=1 SV=2 637 968 2.0E-34
sp|O14127|YF51_SCHPO Uncharacterized protein C3C7.01c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC3C7.01c PE=3 SV=2 181 624 3.0E-33
sp|Q9BT40|INP5K_HUMAN Inositol polyphosphate 5-phosphatase K OS=Homo sapiens GN=INPP5K PE=1 SV=3 694 958 5.0E-29
sp|O80560|IP5PC_ARATH Type I inositol polyphosphate 5-phosphatase 12 OS=Arabidopsis thaliana GN=IP5P12 PE=1 SV=2 637 968 6.0E-29
sp|Q7XZU3|SAC1_ARATH Phosphoinositide phosphatase SAC1 OS=Arabidopsis thaliana GN=SAC1 PE=1 SV=1 196 713 2.0E-28
sp|Q9SKB7|IP5PE_ARATH Type II inositol polyphosphate 5-phosphatase 14 OS=Arabidopsis thaliana GN=IP5P14 PE=1 SV=1 637 968 1.0E-27
sp|Q9SYK4|IP5PD_ARATH Type I inositol polyphosphate 5-phosphatase 13 OS=Arabidopsis thaliana GN=IP5P13 PE=1 SV=1 637 968 1.0E-27
sp|Q8C5L6|INP5K_MOUSE Inositol polyphosphate 5-phosphatase K OS=Mus musculus GN=Inpp5k PE=1 SV=2 678 959 5.0E-27
sp|P42837|FIG4_YEAST Polyphosphoinositide phosphatase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FIG4 PE=1 SV=1 203 624 7.0E-27
sp|Q5EAF2|IP5PB_ARATH Type IV inositol polyphosphate 5-phosphatase 11 OS=Arabidopsis thaliana GN=IP5P11 PE=1 SV=1 778 957 8.0E-27
sp|Q2I6J1|SHP2A_DANRE Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2A OS=Danio rerio GN=inppl1a PE=2 SV=2 659 959 9.0E-26
sp|O15357|SHIP2_HUMAN Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 OS=Homo sapiens GN=INPPL1 PE=1 SV=2 659 974 3.0E-25
sp|Q9WVR3|SHIP2_RAT Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 OS=Rattus norvegicus GN=Inppl1 PE=1 SV=1 659 959 8.0E-25
sp|Q6P549|SHIP2_MOUSE Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 OS=Mus musculus GN=Inppl1 PE=1 SV=1 657 974 8.0E-25
sp|P97573|SHIP1_RAT Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1 OS=Rattus norvegicus GN=Inpp5d PE=1 SV=1 645 959 2.0E-24
sp|Q94A27|SAC2_ARATH Phosphoinositide phosphatase SAC2 OS=Arabidopsis thaliana GN=SAC2 PE=2 SV=1 102 624 3.0E-24
sp|Q9ES52|SHIP1_MOUSE Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1 OS=Mus musculus GN=Inpp5d PE=1 SV=2 645 959 5.0E-24
sp|Q91WF7|FIG4_MOUSE Polyphosphoinositide phosphatase OS=Mus musculus GN=Fig4 PE=1 SV=1 266 624 7.0E-24
sp|Q92835|SHIP1_HUMAN Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1 OS=Homo sapiens GN=INPP5D PE=1 SV=2 645 959 2.0E-23
sp|Q8RW97|SAC5_ARATH Phosphoinositide phosphatase SAC5 OS=Arabidopsis thaliana GN=SAC5 PE=2 SV=1 196 626 2.0E-23
sp|Q6P4S2|SHIP1_XENLA Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1 OS=Xenopus laevis GN=inpp5d PE=2 SV=1 659 959 6.0E-23
sp|Q7XZU2|SAC3_ARATH Phosphoinositide phosphatase SAC3 OS=Arabidopsis thaliana GN=SAC3 PE=2 SV=1 204 624 3.0E-22
sp|Q92562|FIG4_HUMAN Polyphosphoinositide phosphatase OS=Homo sapiens GN=FIG4 PE=1 SV=1 266 624 6.0E-22
sp|P34370|I5P2_CAEEL Inositol polyphosphate 5-phosphatase OS=Caenorhabditis elegans GN=cil-1 PE=1 SV=1 741 954 6.0E-21
sp|Q2I6J0|SHP2B_DANRE Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2B OS=Danio rerio GN=inppl1b PE=2 SV=1 654 958 3.0E-19
sp|Q08227|INP54_YEAST Phosphatidylinositol 4,5-bisphosphate 5-phosphatase INP54 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP54 PE=1 SV=1 691 950 8.0E-15
sp|Q7XZU1|SAC4_ARATH Phosphoinositide phosphatase SAC4 OS=Arabidopsis thaliana GN=SAC4 PE=2 SV=1 204 446 2.0E-11
sp|Q7Z9H9|FIG4_SCHPO Polyphosphoinositide phosphatase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC1093.03 PE=3 SV=3 512 635 9.0E-09
sp|Q7Z9H9|FIG4_SCHPO Polyphosphoinositide phosphatase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC1093.03 PE=3 SV=3 203 357 3.0E-08
sp|Q7XZU1|SAC4_ARATH Phosphoinositide phosphatase SAC4 OS=Arabidopsis thaliana GN=SAC4 PE=2 SV=1 512 624 5.0E-07
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GO

GO Term Description Terminal node
GO:0016791 phosphatase activity Yes
GO:0003824 catalytic activity Yes
GO:0042578 phosphoric ester hydrolase activity No
GO:0003674 molecular_function No
GO:0016787 hydrolase activity No
GO:0016788 hydrolase activity, acting on ester bonds No

Deeploc

Deeploc data not available for this genome

SignalP

(None)

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

(None)

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup4107
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|5044 (this protein)
Ophiocordyceps australis map64 (Brazil) OphauB2|3030
Ophiocordyceps camponoti-floridani Ophcf2|04364
Ophiocordyceps camponoti-rufipedis Ophun1|3043
Ophiocordyceps kimflemingae Ophio5|3153
Ophiocordyceps subramaniannii Hirsu2|8312

Sequences

Type of sequenceSequence
Locus Download genbank file of locus Download genbank file of locus (reverse complement)
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 >OphauG2|5044
MDAQQPPHTSWAAPPPAPEKSSELLIRDYPQRSIAIVSSSHALILRYSSSATETQHNGSHASLASARSRTAESTV
AKCMVEFSPVSQPLLAQYRPLAPRPIYGTLGLMAVDGQVFLSVITRAVRAATVRPGETVERISSVAFYCLSSANY
DDVVPLEPSESDMSEASWAYGNASSFYGQGLGRRDVPPEHPCHDLRKLLSNGSFYYSTDFDVTSRLQARPLNTNS
FEIDNFDDTYLWNSFMISPLVQFRSRLMPPEREALDSSRILTSAIRGFCKTMTIPQSSSPLASGSTSGKPSYLTL
ISRLSCRRAGTRFNSRGIDDDGHVANFVESETTFWSPVGVLFSYAQVRGSVPVFWEQTAELLPGRQKITITRSSE
GTQPVLNKHFEELEHIYGAVHIINLLSETKPAEMELSRLYRQGVRNCPLSRPGVDASPDHALLRETHYDFHAETK
GPAGYEAARDIRHYIERSTDTFAYFLAQEAVDGDGDKEKDRNKSEDEQRRQRGSHLVVVLQQDGVFRTNCLDCLD
RTNLIQTLISQMAIETFLAHRNEYAASDFWMRHASLWADNGDSLSKIYAGTGALKSSFTRHGKMSLAGAVADMRK
SVQRIYHNNFIDPSRQVTIDMLLGRLIGQAAVLLYDPISDYVSVEVARRSDEYTSFEKISIWAGTFNLNGRTQGI
DKDLSPWLLPRSLDADLADVYVVAFQEIVELSPQQIMNSDPSRRHLWESAVKHCLNRRQASRGGVKYVLLRSGQL
VGAALCIFVRASVLCHIKNVEGSVKKTGLSGMAGNKGAVAIRFDFANTHVCFVTAHLAAGFSNYEERNRDYATIH
EGLRFQRNRGIEDHDAIIWLGDFNYRIGLALEATRALMKRGDLGTLYENDQLNLQMVAGLAFHFYSEARISFMPT
YKFDVGTDDYDTSEKARIPAWTDRILKKGAILRQLSYESAPLRFSDHRPVYASFECKVSIVDETLREKISQESYQ
RRKAELGDTTAHVGEDQETEDEDLIGYDAIEPGLPPASSDKHKWWLDHGQPARAHVMAPSGSDGQCMALNPQRPS
NPFGAGDEPDWVSVRRLSVSSLSSSTYEKVPLPPRPGGPATGRPDDVEHGEAAMQPCGTRGQQGRPAPPPPPRMG
ARAGPLDSAIKQQRAAETGSKSPSARLPAPPVAKKPAHLLATKARAKNKTPAATGAATAAVAAAAAAAAGAGAGA
GAGATSDIGANSNGGTRTVAQLAPAWSRASATAARRGGRDGQKTWPRDEEAGNGDESLLDSALDERLGESMRIGG
WEALQPSKS*
Coding >OphauG2|5044
ATGGACGCCCAGCAGCCACCGCATACTTCGTGGGCCGCGCCTCCTCCCGCCCCGGAAAAGTCGAGCGAGCTGCTC
ATCCGCGACTATCCCCAGCGGTCCATTGCCATTGTGTCGTCGTCGCACGCTCTCATCTTGCGCTACAGCTCCTCG
GCGACGGAGACGCAGCACAATGGCTCCCACGCGTCTTTGGCATCGGCCCGATCGCGCACCGCCGAGTCGACTGTT
GCCAAGTGCATGGTGGAGTTTTCCCCCGTTTCGCAGCCGCTCCTTGCCCAGTACCGCCCACTTGCGCCACGGCCG
ATATACGGAACCTTGGGCCTCATGGCCGTTGACGGCCAAGTCTTCCTCTCCGTCATCACACGCGCCGTTAGGGCC
GCCACTGTCCGGCCCGGCGAGACGGTGGAGCGAATATCGAGCGTGGCCTTTTACTGCCTCAGCAGCGCAAATTAC
GACGACGTGGTCCCTCTGGAGCCCAGCGAGTCGGACATGTCCGAGGCCTCTTGGGCATATGGTAACGCTTCCTCG
TTTTACGGTCAGGGTCTCGGTAGGCGCGATGTGCCTCCCGAGCACCCGTGCCACGATTTACGCAAGCTGCTCAGC
AACGGCTCCTTTTATTATAGCACAGACTTCGACGTAACAAGCCGCCTGCAGGCAAGGCCCTTGAATACCAATTCT
TTTGAAATTGACAACTTTGATGACACGTACTTGTGGAACTCGTTCATGATCAGTCCACTTGTTCAGTTCCGCTCG
CGGCTCATGCCCCCCGAGCGCGAGGCCCTGGATTCGTCTCGCATTCTCACGTCGGCCATCCGAGGCTTCTGCAAA
ACCATGACAATACCACAGAGCTCGTCTCCCCTTGCATCAGGCTCTACAAGTGGAAAGCCGTCATATCTGACGCTC
ATATCGCGCCTGTCCTGCAGGCGAGCGGGGACTCGCTTCAACTCTCGAGGCATCGATGACGACGGGCACGTGGCC
AACTTTGTCGAGTCTGAGACGACGTTTTGGAGCCCAGTTGGCGTCTTGTTTTCCTATGCGCAAGTCAGAGGGTCA
GTGCCCGTGTTTTGGGAACAGACTGCCGAGCTGCTGCCAGGGAGGCAGAAAATCACCATCACCAGGTCGTCCGAG
GGCACGCAGCCAGTCCTGAACAAGCACTTTGAGGAACTCGAGCACATTTACGGCGCCGTCCACATCATCAACCTT
CTCAGCGAGACCAAGCCGGCCGAGATGGAGCTGAGCAGGCTGTATCGACAGGGCGTGCGCAACTGTCCATTGAGT
CGGCCTGGCGTCGACGCATCACCAGACCATGCGCTGCTGCGTGAGACGCACTATGATTTTCACGCCGAAACCAAG
GGCCCGGCAGGCTATGAGGCTGCCCGAGATATCCGGCACTACATTGAGCGTTCCACCGACACTTTTGCCTACTTT
CTTGCCCAAGAGGCCGTGGACGGCGACGGCGACAAGGAAAAGGACAGGAACAAGAGCGAGGATGAGCAGAGACGG
CAGCGAGGCAGTCACCTTGTAGTCGTCTTGCAACAGGATGGCGTCTTTCGCACAAACTGTCTGGATTGCCTCGAC
CGCACCAACCTGATTCAGACGCTGATTTCGCAAATGGCCATTGAGACCTTCCTCGCCCACCGCAACGAGTATGCA
GCGTCAGACTTTTGGATGCGGCATGCCAGCCTCTGGGCCGACAATGGCGATTCGCTCTCCAAGATATACGCCGGG
ACGGGTGCACTCAAGTCGTCGTTTACGCGGCACGGCAAGATGTCACTGGCCGGCGCAGTGGCCGACATGCGCAAG
TCGGTCCAGCGAATCTACCACAACAACTTTATTGATCCTTCGCGACAAGTCACGATTGACATGTTACTCGGCCGA
CTCATTGGCCAGGCAGCCGTGCTCCTCTACGACCCCATTAGCGACTATGTCTCAGTCGAGGTGGCTCGGCGTAGC
GACGAGTACACATCCTTTGAGAAGATTAGCATCTGGGCTGGCACTTTTAACCTCAACGGACGCACCCAGGGCATC
GATAAGGATCTTTCGCCCTGGCTTCTGCCCCGGTCCTTGGATGCCGACCTTGCTGATGTCTACGTTGTTGCCTTT
CAGGAAATCGTCGAGCTCAGCCCCCAGCAGATTATGAACAGTGACCCGTCGCGGCGACACTTGTGGGAGAGCGCC
GTCAAGCATTGCCTCAATCGACGGCAGGCGAGCAGAGGAGGAGTCAAGTATGTGCTCCTACGCAGCGGACAGCTC
GTTGGTGCCGCCCTCTGTATCTTTGTCAGAGCGTCGGTTCTCTGCCACATCAAGAACGTCGAGGGCAGCGTCAAG
AAGACAGGACTGTCGGGAATGGCTGGCAACAAGGGAGCCGTTGCCATCCGCTTTGACTTTGCCAACACTCATGTC
TGCTTTGTCACGGCGCACCTGGCAGCTGGCTTCTCCAACTATGAGGAAAGAAATCGCGACTATGCCACCATTCAC
GAGGGGTTGCGTTTCCAGCGCAACAGGGGAATAGAGGACCATGATGCAATCATATGGCTTGGAGACTTCAATTAC
CGCATCGGACTTGCTCTTGAGGCTACCCGGGCCCTGATGAAGAGAGGCGACTTGGGAACGCTCTACGAAAACGAT
CAGCTGAATCTCCAGATGGTGGCGGGGCTGGCCTTTCACTTTTACTCGGAAGCACGCATCAGCTTCATGCCAACG
TACAAATTTGATGTTGGGACCGACGACTACGACACGTCGGAGAAGGCTCGAATACCGGCATGGACGGACAGAATC
TTGAAAAAGGGAGCCATACTACGACAGCTGTCGTACGAGTCGGCGCCACTGAGATTTTCTGACCACCGGCCAGTG
TATGCGTCGTTTGAATGCAAAGTAAGCATTGTGGACGAGACTCTGCGTGAAAAGATTAGCCAAGAGTCGTACCAG
CGACGCAAAGCTGAACTTGGGGATACTACGGCCCACGTGGGCGAGGACCAAGAAACAGAGGACGAAGACCTGATT
GGCTACGATGCCATCGAGCCCGGTCTCCCGCCAGCCAGCTCAGACAAGCACAAATGGTGGCTGGACCATGGGCAG
CCAGCGCGGGCGCACGTCATGGCTCCCAGCGGGAGTGACGGACAGTGCATGGCTCTCAACCCGCAGCGGCCTTCG
AACCCGTTTGGAGCTGGCGACGAGCCCGACTGGGTGTCTGTGCGGCGTCTTTCCGTCTCGAGTCTATCGAGCTCA
ACGTACGAAAAGGTGCCGCTCCCGCCGCGGCCTGGCGGACCGGCAACGGGAAGGCCAGATGATGTTGAGCATGGC
GAGGCGGCAATGCAGCCATGCGGGACTCGAGGACAACAAGGGCGGCCGGCGCCGCCACCGCCACCTCGGATGGGT
GCGCGGGCAGGACCGCTAGACAGTGCAATCAAGCAGCAAAGAGCGGCGGAGACGGGCAGCAAGAGCCCAAGCGCA
AGGCTGCCGGCGCCGCCTGTGGCAAAGAAGCCAGCTCATCTACTGGCTACAAAGGCACGGGCAAAGAACAAGACG
CCTGCAGCGACTGGTGCAGCTACGGCGGCAGTGGCGGCGGCGGCGGCGGCGGCGGCTGGTGCTGGTGCTGGTGCA
GGTGCTGGTGCTACAAGTGATATTGGTGCCAATAGCAATGGTGGGACAAGGACGGTGGCTCAGTTAGCGCCGGCG
TGGTCGAGAGCATCAGCCACGGCAGCGAGGCGAGGGGGACGAGATGGGCAGAAAACATGGCCAAGAGACGAGGAG
GCGGGCAATGGAGACGAGAGTCTGCTGGACTCGGCACTGGACGAGAGGCTTGGAGAGTCGATGCGGATTGGCGGA
TGGGAGGCGCTGCAGCCAAGCAAGAGCTGA
Transcript >OphauG2|5044
ATGGACGCCCAGCAGCCACCGCATACTTCGTGGGCCGCGCCTCCTCCCGCCCCGGAAAAGTCGAGCGAGCTGCTC
ATCCGCGACTATCCCCAGCGGTCCATTGCCATTGTGTCGTCGTCGCACGCTCTCATCTTGCGCTACAGCTCCTCG
GCGACGGAGACGCAGCACAATGGCTCCCACGCGTCTTTGGCATCGGCCCGATCGCGCACCGCCGAGTCGACTGTT
GCCAAGTGCATGGTGGAGTTTTCCCCCGTTTCGCAGCCGCTCCTTGCCCAGTACCGCCCACTTGCGCCACGGCCG
ATATACGGAACCTTGGGCCTCATGGCCGTTGACGGCCAAGTCTTCCTCTCCGTCATCACACGCGCCGTTAGGGCC
GCCACTGTCCGGCCCGGCGAGACGGTGGAGCGAATATCGAGCGTGGCCTTTTACTGCCTCAGCAGCGCAAATTAC
GACGACGTGGTCCCTCTGGAGCCCAGCGAGTCGGACATGTCCGAGGCCTCTTGGGCATATGGTAACGCTTCCTCG
TTTTACGGTCAGGGTCTCGGTAGGCGCGATGTGCCTCCCGAGCACCCGTGCCACGATTTACGCAAGCTGCTCAGC
AACGGCTCCTTTTATTATAGCACAGACTTCGACGTAACAAGCCGCCTGCAGGCAAGGCCCTTGAATACCAATTCT
TTTGAAATTGACAACTTTGATGACACGTACTTGTGGAACTCGTTCATGATCAGTCCACTTGTTCAGTTCCGCTCG
CGGCTCATGCCCCCCGAGCGCGAGGCCCTGGATTCGTCTCGCATTCTCACGTCGGCCATCCGAGGCTTCTGCAAA
ACCATGACAATACCACAGAGCTCGTCTCCCCTTGCATCAGGCTCTACAAGTGGAAAGCCGTCATATCTGACGCTC
ATATCGCGCCTGTCCTGCAGGCGAGCGGGGACTCGCTTCAACTCTCGAGGCATCGATGACGACGGGCACGTGGCC
AACTTTGTCGAGTCTGAGACGACGTTTTGGAGCCCAGTTGGCGTCTTGTTTTCCTATGCGCAAGTCAGAGGGTCA
GTGCCCGTGTTTTGGGAACAGACTGCCGAGCTGCTGCCAGGGAGGCAGAAAATCACCATCACCAGGTCGTCCGAG
GGCACGCAGCCAGTCCTGAACAAGCACTTTGAGGAACTCGAGCACATTTACGGCGCCGTCCACATCATCAACCTT
CTCAGCGAGACCAAGCCGGCCGAGATGGAGCTGAGCAGGCTGTATCGACAGGGCGTGCGCAACTGTCCATTGAGT
CGGCCTGGCGTCGACGCATCACCAGACCATGCGCTGCTGCGTGAGACGCACTATGATTTTCACGCCGAAACCAAG
GGCCCGGCAGGCTATGAGGCTGCCCGAGATATCCGGCACTACATTGAGCGTTCCACCGACACTTTTGCCTACTTT
CTTGCCCAAGAGGCCGTGGACGGCGACGGCGACAAGGAAAAGGACAGGAACAAGAGCGAGGATGAGCAGAGACGG
CAGCGAGGCAGTCACCTTGTAGTCGTCTTGCAACAGGATGGCGTCTTTCGCACAAACTGTCTGGATTGCCTCGAC
CGCACCAACCTGATTCAGACGCTGATTTCGCAAATGGCCATTGAGACCTTCCTCGCCCACCGCAACGAGTATGCA
GCGTCAGACTTTTGGATGCGGCATGCCAGCCTCTGGGCCGACAATGGCGATTCGCTCTCCAAGATATACGCCGGG
ACGGGTGCACTCAAGTCGTCGTTTACGCGGCACGGCAAGATGTCACTGGCCGGCGCAGTGGCCGACATGCGCAAG
TCGGTCCAGCGAATCTACCACAACAACTTTATTGATCCTTCGCGACAAGTCACGATTGACATGTTACTCGGCCGA
CTCATTGGCCAGGCAGCCGTGCTCCTCTACGACCCCATTAGCGACTATGTCTCAGTCGAGGTGGCTCGGCGTAGC
GACGAGTACACATCCTTTGAGAAGATTAGCATCTGGGCTGGCACTTTTAACCTCAACGGACGCACCCAGGGCATC
GATAAGGATCTTTCGCCCTGGCTTCTGCCCCGGTCCTTGGATGCCGACCTTGCTGATGTCTACGTTGTTGCCTTT
CAGGAAATCGTCGAGCTCAGCCCCCAGCAGATTATGAACAGTGACCCGTCGCGGCGACACTTGTGGGAGAGCGCC
GTCAAGCATTGCCTCAATCGACGGCAGGCGAGCAGAGGAGGAGTCAAGTATGTGCTCCTACGCAGCGGACAGCTC
GTTGGTGCCGCCCTCTGTATCTTTGTCAGAGCGTCGGTTCTCTGCCACATCAAGAACGTCGAGGGCAGCGTCAAG
AAGACAGGACTGTCGGGAATGGCTGGCAACAAGGGAGCCGTTGCCATCCGCTTTGACTTTGCCAACACTCATGTC
TGCTTTGTCACGGCGCACCTGGCAGCTGGCTTCTCCAACTATGAGGAAAGAAATCGCGACTATGCCACCATTCAC
GAGGGGTTGCGTTTCCAGCGCAACAGGGGAATAGAGGACCATGATGCAATCATATGGCTTGGAGACTTCAATTAC
CGCATCGGACTTGCTCTTGAGGCTACCCGGGCCCTGATGAAGAGAGGCGACTTGGGAACGCTCTACGAAAACGAT
CAGCTGAATCTCCAGATGGTGGCGGGGCTGGCCTTTCACTTTTACTCGGAAGCACGCATCAGCTTCATGCCAACG
TACAAATTTGATGTTGGGACCGACGACTACGACACGTCGGAGAAGGCTCGAATACCGGCATGGACGGACAGAATC
TTGAAAAAGGGAGCCATACTACGACAGCTGTCGTACGAGTCGGCGCCACTGAGATTTTCTGACCACCGGCCAGTG
TATGCGTCGTTTGAATGCAAAGTAAGCATTGTGGACGAGACTCTGCGTGAAAAGATTAGCCAAGAGTCGTACCAG
CGACGCAAAGCTGAACTTGGGGATACTACGGCCCACGTGGGCGAGGACCAAGAAACAGAGGACGAAGACCTGATT
GGCTACGATGCCATCGAGCCCGGTCTCCCGCCAGCCAGCTCAGACAAGCACAAATGGTGGCTGGACCATGGGCAG
CCAGCGCGGGCGCACGTCATGGCTCCCAGCGGGAGTGACGGACAGTGCATGGCTCTCAACCCGCAGCGGCCTTCG
AACCCGTTTGGAGCTGGCGACGAGCCCGACTGGGTGTCTGTGCGGCGTCTTTCCGTCTCGAGTCTATCGAGCTCA
ACGTACGAAAAGGTGCCGCTCCCGCCGCGGCCTGGCGGACCGGCAACGGGAAGGCCAGATGATGTTGAGCATGGC
GAGGCGGCAATGCAGCCATGCGGGACTCGAGGACAACAAGGGCGGCCGGCGCCGCCACCGCCACCTCGGATGGGT
GCGCGGGCAGGACCGCTAGACAGTGCAATCAAGCAGCAAAGAGCGGCGGAGACGGGCAGCAAGAGCCCAAGCGCA
AGGCTGCCGGCGCCGCCTGTGGCAAAGAAGCCAGCTCATCTACTGGCTACAAAGGCACGGGCAAAGAACAAGACG
CCTGCAGCGACTGGTGCAGCTACGGCGGCAGTGGCGGCGGCGGCGGCGGCGGCGGCTGGTGCTGGTGCTGGTGCA
GGTGCTGGTGCTACAAGTGATATTGGTGCCAATAGCAATGGTGGGACAAGGACGGTGGCTCAGTTAGCGCCGGCG
TGGTCGAGAGCATCAGCCACGGCAGCGAGGCGAGGGGGACGAGATGGGCAGAAAACATGGCCAAGAGACGAGGAG
GCGGGCAATGGAGACGAGAGTCTGCTGGACTCGGCACTGGACGAGAGGCTTGGAGAGTCGATGCGGATTGGCGGA
TGGGAGGCGCTGCAGCCAAGCAAGAGCTGA
Gene >OphauG2|5044
ATGGACGCCCAGCAGCCACCGCATACTTCGTGGGCCGCGCCTCCTCCCGCCCCGGAAAAGTCGAGCGAGCTGCTC
ATCCGCGACTATCCCCAGCGGTCCATTGCCATTGTGTCGTCGTCGCACGCTCTCATCTTGCGCTACAGCTCCTCG
GCGACGGAGACGCAGCACAATGGCTCCCACGCGTCTTTGGCATCGGCCCGATCGCGCACCGCCGAGTCGACTGTT
GCCAAGTGCATGGTGGAGTTTTCCCCCGTTTCGCAGCCGCTCCTTGCCCAGTACCGCCCACTTGCGCCACGGCCG
ATATACGGAACCTTGGGCCTCATGGCCGTTGACGGCCAAGTCTTCCTCTCCGTCATCACACGCGCCGTTAGGGCC
GCCACTGTCCGGCCCGGCGAGACGGTGGAGCGAATATCGAGCGTGGCCTTTTACTGCCTCAGCAGCGCAAATTAC
GACGACGTGGTCCCTCTGGAGCCCAGCGAGTCGGACATGTCCGAGGCCTCTTGGGCATATGGTAACGCTTCCTCG
TTTTACGGTCAGGGTCTCGGTAGGCGCGATGTGCCTCCCGAGCACCCGTGCCACGATTTACGCAAGCTGCTCAGC
AACGGCTCCTTTTATTATAGCACAGACTTCGACGTAACAAGCCGCCTGCAGGCAAGGTAATGCCGTCATGGTCTC
GCCAAACCGTCTCTTGTTTGCTGACCATGACTGCCAAGGCCCTTGAATACCAATTCTTTTGAAATTGACAACTTT
GATGACACGTACTTGTGGAACTCGTTCATGATCAGTCCACTTGTTCAGTTCCGCTCGCGGCTCATGCCCCCCGAG
CGCGAGGCCCTGGATTCGTCTCGCATTCTCACGTCGGCCATCCGAGGCTTCTGCAAAACCATGACAATACCACAG
AGCTCGTCTCCCCTTGCATCAGGCTCTACAAGTGGAAAGCCGTCATATCTGACGCTCATATCGCGCCTGTCCTGC
AGGCGAGCGGGGACTCGCTTCAACTCTCGAGGCATCGATGACGACGGGCACGTGGCCAACTTTGTCGAGTCTGAG
ACGACGTTTTGGAGCCCAGTTGGCGTCTTGTTTTCCTATGCGCAAGTCAGAGGGTCAGTGCCCGTGTTTTGGGAA
CAGACTGCCGAGCTGCTGCCAGGGAGGCAGAAAATCACCATCACCAGGTCGTCCGAGGGCACGCAGCCAGTCCTG
AACAAGCACTTTGAGGAACTCGAGCACATTTACGGCGCCGTCCACATCATCAACCTTCTCAGCGAGACCAAGCCG
GCCGAGATGGAGCTGAGCAGGCTGTATCGACAGGGCGTGCGCAACTGTCCATTGAGTCGGCCTGGCGTCGACGCA
TCACCAGACCATGCGCTGCTGCGTGAGACGCACTATGATTTTCACGCCGAAACCAAGGGCCCGGCAGGCTATGAG
GCTGCCCGAGATATCCGGCACTACATTGAGCGTTCCACCGACACTTTTGCCTACTTTCTTGCCCAAGAGGCCGTG
GACGGCGACGGCGACAAGGAAAAGGACAGGAACAAGAGCGAGGATGAGCAGAGACGGCAGCGAGGCAGTCACCTT
GTAGTCGTCTTGCAACAGGATGGCGTCTTTCGCACAAACTGTCTGGATTGCCTCGACCGCACCAACCTGATTCAG
ACGCTGATTTCGCAAATGGCCATTGAGACCTTCCTCGCCCACCGCAACGAGTATGCAGCGTCAGACTTTTGGATG
CGGCATGCCAGCCTCTGGGCCGACAATGGCGATTCGCTCTCCAAGATATACGCCGGGACGGGTGCACTCAAGTCG
TCGTTTACGCGGCACGGCAAGATGTCACTGGCCGGCGCAGTGGCCGACATGCGCAAGTCGGTCCAGCGAATCTAC
CACAACAACTTTATTGATCCTTCGCGACAAGTCACGATTGACATGTTACTCGGCCGACTCATTGGCCAGGCAGCC
GTGCTCCTCTACGACCCCATTAGCGACTATGTCTCAGTCGAGGTGGCTCGGCGTAGCGACGAGTACACATCCTTT
GAGAAGATTAGCATCTGGGCTGGCACTTTTAACCTCAACGGACGCACCCAGGGCATCGATAAGGATCTTTCGCCC
TGGCTTCTGCCCCGGTCCTTGGATGCCGACCTTGCTGATGTCTACGTTGTTGCCTTTCAGGAAATCGTCGAGCTC
AGCCCCCAGCAGATTATGAACAGTGACCCGTCGCGGCGACACTTGTGGGAGAGCGCCGTCAAGCATTGCCTCAAT
CGACGGCAGGCGAGCAGAGGAGGAGTCAAGTATGTGCTCCTACGCAGCGGACAGCTCGTTGGTGCCGCCCTCTGT
ATCTTTGTCAGAGCGTCGGTTCTCTGCCACATCAAGAACGTCGAGGGCAGCGTCAAGAAGACAGGACTGTCGGGA
ATGGCTGGCAACAAGGGAGCCGTTGCCATCCGCTTTGACTTTGCCAACACTCATGTCTGCTTTGTCACGGCGCAC
CTGGCAGCTGGCTTCTCCAACTATGAGGAAAGAAATCGCGACTATGCCACCATTCACGAGGGGTTGCGTTTCCAG
CGCAACAGGGGAATAGAGGACCATGGTAAGCCTTGGACAGGGCGAGGGCGCATTGGGACTGTCTGCTAAAGTAGC
TGCGTGGGTAGATGCAATCATATGGCTTGGAGACTTCAATTACCGCATCGGACTTGCTCTTGAGGCTACCCGGGC
CCTGATGAAGAGAGGCGACTTGGGAACGCTCTACGAAAACGATCAGCTGAATCTCCAGATGGTGGCGGGGCTGGC
CTTTCACTTTTACTCGGAAGCACGCATCAGCTTCATGCCAACGTACAAATTTGATGTTGGGACCGACGACTACGA
CACGTCGTGAGTCTGGGCACCACCACATGCGAGAGAGACGACACGGGCTGACAGCAGGCATTATCAGGGAGAAGG
CTCGAATACCGGCATGGACGGACAGAATCTTGAAAAAGGGAGCCATACTACGACAGCTGTCGTACGAGTCGGCGC
CACTGAGATTTTCTGACCACCGGCCAGTGTATGCGTCGTTTGAATGCAAAGTAAGCATTGTGGACGAGACTCTGC
GTGAAAAGATTAGCCAAGAGTCGTACCAGCGACGCAAAGCTGAACTTGGGGATACTACGGCCCACGTGGGCGAGG
ACCAAGAAACAGAGGACGAAGACCTGATTGGCTACGATGCCATCGAGCCCGGTCTCCCGCCAGCCAGCTCAGACA
AGCACAAATGGTGGCTGGACCATGGGCAGCCAGCGCGGGCGCACGTCATGGCTCCCAGCGGGAGTGACGGACAGT
GCATGGCTCTCAACCCGCAGCGGCCTTCGAACCCGTTTGGAGCTGGCGACGAGCCCGACTGGGTGTCTGTGCGGC
GTCTTTCCGTCTCGAGTCTATCGAGCTCAACGTACGAAAAGGTGCCGCTCCCGCCGCGGCCTGGCGGACCGGCAA
CGGGAAGGCCAGATGATGTTGAGCATGGCGAGGCGGCAATGCAGCCATGCGGGACTCGAGGACAACAAGGGCGGC
CGGCGCCGCCACCGCCACCTCGGATGGGTGCGCGGGCAGGACCGCTAGACAGTGCAATCAAGCAGCAAAGAGCGG
CGGAGACGGGCAGCAAGAGCCCAAGCGCAAGGCTGCCGGCGCCGCCTGTGGCAAAGAAGCCAGCTCATCTACTGG
CTACAAAGGCACGGGCAAAGAACAAGACGCCTGCAGCGACTGGTGCAGCTACGGCGGCAGTGGCGGCGGCGGCGG
CGGCGGCGGCTGGTGCTGGTGCTGGTGCAGGTGCTGGTGCTACAAGTGATATTGGTGCCAATAGCAATGGTGGGA
CAAGGACGGTGGCTCAGTTAGCGCCGGCGTGGTCGAGAGCATCAGCCACGGCAGCGAGGCGAGGGGGACGAGATG
GGCAGAAAACATGGCCAAGAGACGAGGAGGCGGGCAATGGAGACGAGAGTCTGCTGGACTCGGCACTGGACGAGA
GGCTTGGAGAGTCGATGCGGATTGGCGGATGGGAGGCGCTGCAGCCAAGCAAGAGCTGA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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