Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|3446
Gene name
LocationContig_19:64739..67682
Strand+
Gene length (bp)2943
Transcript length (bp)2943
Coding sequence length (bp)2943
Protein length (aa) 981

Overview

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PFAM Domains

(None)

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|D3ZGS3|OCRL_RAT Inositol polyphosphate 5-phosphatase OCRL-1 OS=Rattus norvegicus GN=Ocrl PE=1 SV=1 492 900 4.0E-21
sp|Q6NVF0|OCRL_MOUSE Inositol polyphosphate 5-phosphatase OCRL-1 OS=Mus musculus GN=Ocrl PE=1 SV=1 492 900 9.0E-21
sp|Q01968|OCRL_HUMAN Inositol polyphosphate 5-phosphatase OCRL-1 OS=Homo sapiens GN=OCRL PE=1 SV=3 456 927 1.0E-20
sp|Q8K337|I5P2_MOUSE Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Mus musculus GN=Inpp5b PE=1 SV=1 492 721 2.0E-19
sp|P32019|I5P2_HUMAN Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Homo sapiens GN=INPP5B PE=1 SV=4 492 721 2.0E-19
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|D3ZGS3|OCRL_RAT Inositol polyphosphate 5-phosphatase OCRL-1 OS=Rattus norvegicus GN=Ocrl PE=1 SV=1 492 900 4.0E-21
sp|Q6NVF0|OCRL_MOUSE Inositol polyphosphate 5-phosphatase OCRL-1 OS=Mus musculus GN=Ocrl PE=1 SV=1 492 900 9.0E-21
sp|Q01968|OCRL_HUMAN Inositol polyphosphate 5-phosphatase OCRL-1 OS=Homo sapiens GN=OCRL PE=1 SV=3 456 927 1.0E-20
sp|Q8K337|I5P2_MOUSE Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Mus musculus GN=Inpp5b PE=1 SV=1 492 721 2.0E-19
sp|P32019|I5P2_HUMAN Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Homo sapiens GN=INPP5B PE=1 SV=4 492 721 2.0E-19
sp|Q0WT19|IP5P8_ARATH Type I inositol polyphosphate 5-phosphatase 8 OS=Arabidopsis thaliana GN=IP5P8 PE=2 SV=1 112 282 3.0E-19
sp|D3ZGS3|OCRL_RAT Inositol polyphosphate 5-phosphatase OCRL-1 OS=Rattus norvegicus GN=Ocrl PE=1 SV=1 25 295 2.0E-18
sp|Q6NVF0|OCRL_MOUSE Inositol polyphosphate 5-phosphatase OCRL-1 OS=Mus musculus GN=Ocrl PE=1 SV=1 25 303 2.0E-18
sp|Q62910|SYNJ1_RAT Synaptojanin-1 OS=Rattus norvegicus GN=Synj1 PE=1 SV=3 23 294 2.0E-17
sp|O43426|SYNJ1_HUMAN Synaptojanin-1 OS=Homo sapiens GN=SYNJ1 PE=1 SV=2 9 294 3.0E-17
sp|Q8CHC4|SYNJ1_MOUSE Synaptojanin-1 OS=Mus musculus GN=Synj1 PE=1 SV=3 23 294 3.0E-17
sp|O18964|SYNJ1_BOVIN Synaptojanin-1 (Fragment) OS=Bos taurus GN=SYNJ1 PE=1 SV=2 9 294 3.0E-17
sp|Q9SIS4|IP5P9_ARATH Type IV inositol polyphosphate 5-phosphatase 9 OS=Arabidopsis thaliana GN=IP5P9 PE=1 SV=1 115 294 5.0E-17
sp|Q9JMC1|PI5PA_RAT Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A OS=Rattus norvegicus GN=Inpp5j PE=1 SV=1 105 283 2.0E-16
sp|Q9FUR2|IP5P2_ARATH Type I inositol polyphosphate 5-phosphatase 2 OS=Arabidopsis thaliana GN=IP5P2 PE=1 SV=2 159 295 2.0E-16
sp|Q0WQ41|IP5P7_ARATH Type IV inositol polyphosphate 5-phosphatase 7 OS=Arabidopsis thaliana GN=IP5P7 PE=1 SV=1 126 282 2.0E-16
sp|P59644|PI5PA_MOUSE Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A OS=Mus musculus GN=Inpp5j PE=1 SV=2 115 283 3.0E-16
sp|Q12271|INP53_YEAST Polyphosphatidylinositol phosphatase INP53 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP53 PE=1 SV=1 115 303 4.0E-16
sp|Q01968|OCRL_HUMAN Inositol polyphosphate 5-phosphatase OCRL-1 OS=Homo sapiens GN=OCRL PE=1 SV=3 25 295 5.0E-16
sp|Q84MA2|IP5P1_ARATH Type I inositol polyphosphate 5-phosphatase 1 OS=Arabidopsis thaliana GN=IP5P1 PE=1 SV=2 133 283 8.0E-16
sp|Q8GTS0|IP5P4_ARATH Type I inositol polyphosphate 5-phosphatase 4 OS=Arabidopsis thaliana GN=IP5P4 PE=2 SV=1 159 282 1.0E-15
sp|Q8C5L6|INP5K_MOUSE Inositol polyphosphate 5-phosphatase K OS=Mus musculus GN=Inpp5k PE=1 SV=2 77 283 1.0E-15
sp|Q9LR47|IP5P6_ARATH Type IV inositol polyphosphate 5-phosphatase 6 OS=Arabidopsis thaliana GN=IP5P6 PE=1 SV=2 159 282 2.0E-15
sp|Q15735|PI5PA_HUMAN Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A OS=Homo sapiens GN=INPP5J PE=1 SV=3 115 283 2.0E-15
sp|Q66GQ6|IP5P5_ARATH Type I inositol polyphosphate 5-phosphatase 5 OS=Arabidopsis thaliana GN=IP5P5 PE=2 SV=1 159 294 2.0E-15
sp|Q9BT40|INP5K_HUMAN Inositol polyphosphate 5-phosphatase K OS=Homo sapiens GN=INPP5K PE=1 SV=3 115 283 9.0E-15
sp|P32019|I5P2_HUMAN Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Homo sapiens GN=INPP5B PE=1 SV=4 115 294 1.0E-14
sp|Q8H0Z6|IP5P3_ARATH Type IV inositol polyphosphate 5-phosphatase 3 OS=Arabidopsis thaliana GN=IP5P3 PE=1 SV=1 157 282 1.0E-14
sp|Q8K337|I5P2_MOUSE Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Mus musculus GN=Inpp5b PE=1 SV=1 115 294 2.0E-14
sp|P50942|INP52_YEAST Polyphosphatidylinositol phosphatase INP52 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP52 PE=1 SV=1 117 303 6.0E-14
sp|Q9D2G5|SYNJ2_MOUSE Synaptojanin-2 OS=Mus musculus GN=Synj2 PE=1 SV=2 20 283 1.0E-13
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 34 282 2.0E-13
sp|O15056|SYNJ2_HUMAN Synaptojanin-2 OS=Homo sapiens GN=SYNJ2 PE=1 SV=3 20 283 2.0E-13
sp|O55207|SYNJ2_RAT Synaptojanin-2 OS=Rattus norvegicus GN=Synj2 PE=1 SV=2 18 283 3.0E-13
sp|O15357|SHIP2_HUMAN Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 OS=Homo sapiens GN=INPPL1 PE=1 SV=2 44 303 4.0E-12
sp|Q9WVR3|SHIP2_RAT Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 OS=Rattus norvegicus GN=Inppl1 PE=1 SV=1 44 303 5.0E-12
sp|A8MR21|IP5PA_ARATH Type I inositol polyphosphate 5-phosphatase 10 OS=Arabidopsis thaliana GN=IP5P10 PE=2 SV=1 151 282 7.0E-12
sp|Q6P549|SHIP2_MOUSE Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 OS=Mus musculus GN=Inppl1 PE=1 SV=1 44 303 7.0E-12
sp|Q8K337|I5P2_MOUSE Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Mus musculus GN=Inpp5b PE=1 SV=1 367 435 7.0E-11
sp|Q2I6J1|SHP2A_DANRE Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2A OS=Danio rerio GN=inppl1a PE=2 SV=2 44 303 1.0E-10
sp|Q9USQ6|SYJ2_SCHPO Inositol-1,4,5-trisphosphate 5-phosphatase 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=syj2 PE=2 SV=1 115 296 5.0E-10
sp|O14306|YE8A_SCHPO Probable inositol polyphosphate 5-phosphatase C9G1.10c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC9G1.10c PE=1 SV=2 115 294 6.0E-10
sp|P40559|INP51_YEAST Phosphatidylinositol 4,5-bisphosphate 5-phosphatase INP51 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP51 PE=1 SV=1 115 292 1.0E-09
sp|Q9WVR1|INP5E_RAT 72 kDa inositol polyphosphate 5-phosphatase OS=Rattus norvegicus GN=Inpp5e PE=1 SV=2 361 434 3.0E-09
sp|Q2I6J0|SHP2B_DANRE Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2B OS=Danio rerio GN=inppl1b PE=2 SV=1 136 283 3.0E-09
sp|Q9JII1|INP5E_MOUSE 72 kDa inositol polyphosphate 5-phosphatase OS=Mus musculus GN=Inpp5e PE=1 SV=1 372 434 4.0E-09
sp|A0FI79|INP5E_PANTR 72 kDa inositol polyphosphate 5-phosphatase OS=Pan troglodytes GN=INPP5E PE=2 SV=1 372 434 7.0E-09
sp|Q9NRR6|INP5E_HUMAN 72 kDa inositol polyphosphate 5-phosphatase OS=Homo sapiens GN=INPP5E PE=1 SV=2 372 434 7.0E-09
sp|Q12271|INP53_YEAST Polyphosphatidylinositol phosphatase INP53 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP53 PE=1 SV=1 367 432 8.0E-09
sp|P32019|I5P2_HUMAN Type II inositol 1,4,5-trisphosphate 5-phosphatase OS=Homo sapiens GN=INPP5B PE=1 SV=4 373 435 1.0E-08
sp|Q84W55|IP5PF_ARATH Type II inositol polyphosphate 5-phosphatase 15 OS=Arabidopsis thaliana GN=IP5P15 PE=1 SV=2 353 439 1.0E-08
sp|P50942|INP52_YEAST Polyphosphatidylinositol phosphatase INP52 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INP52 PE=1 SV=1 370 432 2.0E-08
sp|Q9SKB7|IP5PE_ARATH Type II inositol polyphosphate 5-phosphatase 14 OS=Arabidopsis thaliana GN=IP5P14 PE=1 SV=1 369 432 2.0E-08
sp|Q5EAF2|IP5PB_ARATH Type IV inositol polyphosphate 5-phosphatase 11 OS=Arabidopsis thaliana GN=IP5P11 PE=1 SV=1 357 434 2.0E-08
sp|Q6P4S2|SHIP1_XENLA Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1 OS=Xenopus laevis GN=inpp5d PE=2 SV=1 44 289 3.0E-08
sp|Q9SYK4|IP5PD_ARATH Type I inositol polyphosphate 5-phosphatase 13 OS=Arabidopsis thaliana GN=IP5P13 PE=1 SV=1 38 295 6.0E-08
sp|Q8CHC4|SYNJ1_MOUSE Synaptojanin-1 OS=Mus musculus GN=Synj1 PE=1 SV=3 367 585 6.0E-08
sp|Q62910|SYNJ1_RAT Synaptojanin-1 OS=Rattus norvegicus GN=Synj1 PE=1 SV=3 367 557 7.0E-08
sp|Q9SYK4|IP5PD_ARATH Type I inositol polyphosphate 5-phosphatase 13 OS=Arabidopsis thaliana GN=IP5P13 PE=1 SV=1 367 432 8.0E-08
sp|Q6NVF0|OCRL_MOUSE Inositol polyphosphate 5-phosphatase OCRL-1 OS=Mus musculus GN=Ocrl PE=1 SV=1 370 432 1.0E-07
sp|O43426|SYNJ1_HUMAN Synaptojanin-1 OS=Homo sapiens GN=SYNJ1 PE=1 SV=2 367 557 1.0E-07
sp|O80560|IP5PC_ARATH Type I inositol polyphosphate 5-phosphatase 12 OS=Arabidopsis thaliana GN=IP5P12 PE=1 SV=2 367 432 1.0E-07
sp|D3ZGS3|OCRL_RAT Inositol polyphosphate 5-phosphatase OCRL-1 OS=Rattus norvegicus GN=Ocrl PE=1 SV=1 370 432 2.0E-07
sp|Q01968|OCRL_HUMAN Inositol polyphosphate 5-phosphatase OCRL-1 OS=Homo sapiens GN=OCRL PE=1 SV=3 370 432 2.0E-07
sp|Q9FUR2|IP5P2_ARATH Type I inositol polyphosphate 5-phosphatase 2 OS=Arabidopsis thaliana GN=IP5P2 PE=1 SV=2 367 431 2.0E-07
sp|O18964|SYNJ1_BOVIN Synaptojanin-1 (Fragment) OS=Bos taurus GN=SYNJ1 PE=1 SV=2 367 557 2.0E-07
sp|O43001|SYJ1_SCHPO Inositol-1,4,5-trisphosphate 5-phosphatase 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=syj1 PE=1 SV=1 363 432 3.0E-07
sp|Q9USQ6|SYJ2_SCHPO Inositol-1,4,5-trisphosphate 5-phosphatase 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=syj2 PE=2 SV=1 370 430 4.0E-07
sp|O55207|SYNJ2_RAT Synaptojanin-2 OS=Rattus norvegicus GN=Synj2 PE=1 SV=2 373 442 4.0E-07
sp|Q9SKB7|IP5PE_ARATH Type II inositol polyphosphate 5-phosphatase 14 OS=Arabidopsis thaliana GN=IP5P14 PE=1 SV=1 26 295 4.0E-07
sp|O15056|SYNJ2_HUMAN Synaptojanin-2 OS=Homo sapiens GN=SYNJ2 PE=1 SV=3 373 435 6.0E-07
sp|Q9D2G5|SYNJ2_MOUSE Synaptojanin-2 OS=Mus musculus GN=Synj2 PE=1 SV=2 373 442 7.0E-07
sp|Q0WT19|IP5P8_ARATH Type I inositol polyphosphate 5-phosphatase 8 OS=Arabidopsis thaliana GN=IP5P8 PE=2 SV=1 371 432 1.0E-06
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GO

(None)

Deeploc

[Help with interpreting the results of Deeploc 2.0]
Localizations Signals Cytoplasm Nucleus Extracellular Cell membrane Mitochondrion Plastid Endoplasmic reticulum Lysosome vacuole Golgi apparatus Peroxisome
Cytoplasm|Nucleus Nuclear export signal 0.6344 0.542 0.0947 0.0698 0.1008 0.013 0.1661 0.3029 0.4009 0.0059

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
Orthogroup2429
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|1554
Ophiocordyceps australis map64 (Brazil) OphauB2|4799
Ophiocordyceps camponoti-floridani Ophcf2|03036
Ophiocordyceps camponoti-rufipedis Ophun1|7281
Ophiocordyceps kimflemingae Ophio5|5770
Ophiocordyceps subramaniannii Hirsu2|3446 (this protein)

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 >Hirsu2|3446
MSASSSASSSGSVGSEPVDLSTTPQSLARAVLARRGEYVRRRSMRVKIGTWNVAACPGTDKDLASWFVDGRGLDK
SLAAVDLSRNPAVDGNGSATADAGSGSGSVRLVGGEDIGLYVLGLQEVVDLNGTREYMNRAVYTDNGPMQKWQAA
VEAMLPPGYELVVAEQMTGILLLVYASPDVAPTISNVSTKQVGTGLLGYFGNKGAVTTRLVLGEATRIVLVNCHL
ASGANPSYLDRRCWDVGQILAKTQFEPVVHGGVAEDDGDKVGDEDFAFWFGDLNFRLDGLPGEDIRRLLTLHTRG
EYDLSQDRPPLPLGGDPFIVMKSCESDDDTSTIPSTHSRDQSFDSKSSLPDPDDFPQDASQDPTSLQATLDSLLP
HDQLRRVIAERKVFHDGWREGHIGFLPSYKYDVGTVGLFDSSEKQRAPSWCDRILFRTRKDKRGYDKQIQDEEAA
RQKDEEMKSRGIHEDDDVLFSYDPDTDGEEQPKGNPGIDYDEYDETAEDGDGEAAETKDGFVDRIYQEIYASHQR
ITSSDHKPVVSVFSLDYDAVVPELKAQVHAEVARELDRAENEGRPGITIVVEGDKGQHESAVDFGDLAFLERKSS
TVTIANTGGVSASFSFVERPTTEDGEPTTTSWLTTSFVRTDGDATDQLGKTVTLEPGETVLAHLEAHVLAAAQLR
ALNDGQLKLEDILVLRVEDGRDHFIPVRAAWLPTCFGRSVDELIRIPDGGIRKFAREKGIQGAISYDAEVHRSAP
KELFQLTEAVQTLAERCVADETMLEDMELPRDPGWPLEPSSWTAGVAEQSSVKGDIVAALDTDRPIFEALPVEMS
SAHKLELVSAILLLFLTSLTDGLVPPHLWAKLSASLPSLTALPAAAWPDIRSQALDMLSTAPNHNIAFIFLTATM
SRVAAELSPGTAEGSRLSGLGRRLSFRRGDEDGSKKRRAREKKYAEVLGPLTFRANDKDKAMKDKERLLLEMFLS
REARS*
Coding >Hirsu2|3446
ATGTCGGCCTCATCCAGCGCGTCGTCCTCGGGCTCCGTCGGCTCGGAGCCGGTGGACCTATCGACGACTCCGCAG
TCGCTGGCCAGGGCCGTCCTGGCCCGGCGCGGCGAATACGTGCGCCGGCGCAGCATGCGTGTCAAGATCGGCACC
TGGAACGTCGCCGCCTGCCCCGGCACCGACAAAGACCTGGCCAGCTGGTTCGTCGACGGTCGCGGCCTCGACAAG
AGCCTGGCTGCCGTCGACCTCTCCCGCAACCCGGCCGTCGACGGCAACGGCTCCGCCACGGCCGACGCCGGCTCC
GGCTCCGGCTCCGTTCGCCTGGTCGGCGGAGAAGACATCGGCCTCTACGTGCTGGGGCTGCAAGAGGTCGTCGAC
CTCAACGGGACGAGGGAATACATGAACCGCGCCGTCTACACCGACAACGGCCCGATGCAGAAGTGGCAGGCAGCG
GTCGAGGCCATGCTGCCTCCCGGGTACGAGCTCGTCGTCGCCGAGCAGATGACGGGCATCCTCCTCCTCGTCTAC
GCCTCTCCCGACGTCGCGCCCACCATCAGCAACGTGAGCACCAAGCAGGTCGGCACAGGGCTCCTTGGCTACTTT
GGAAACAAGGGCGCCGTCACCACCCGGCTCGTCCTGGGCGAGGCGACTCGCATCGTCCTCGTCAACTGCCATCTC
GCTAGTGGCGCCAACCCCAGCTACCTCGACCGGCGCTGCTGGGACGTCGGCCAGATTCTGGCCAAGACGCAGTTC
GAGCCCGTCGTGCACGGGGGCGTGGCCGAGGACGACGGCGACAAGGTCGGCGACGAGGACTTTGCTTTTTGGTTT
GGCGACCTCAACTTCCGCCTCGACGGCCTGCCGGGCGAAGACATAAGGAGGCTGCTGACGCTGCACACGCGCGGC
GAATACGACCTGAGCCAGGACCGGCCTCCTCTTCCGCTGGGCGGCGATCCGTTCATCGTCATGAAAAGCTGCGAG
AGCGACGATGACACGAGCACGATTCCCTCGACGCATTCGCGAGACCAGAGCTTCGACTCTAAGAGCTCGCTGCCC
GACCCCGACGATTTCCCCCAGGATGCAAGCCAGGATCCGACGTCCCTGCAGGCAACCCTGGACTCACTGCTGCCC
CACGACCAGCTGAGGCGCGTCATAGCCGAGCGCAAAGTCTTCCATGACGGCTGGAGGGAAGGCCACATCGGCTTC
CTCCCATCGTACAAGTACGACGTCGGCACCGTTGGCCTGTTCGATTCGAGCGAGAAGCAGCGCGCCCCCAGCTGG
TGCGATCGGATTCTCTTCCGAACCCGCAAGGACAAGAGGGGGTACGACAAGCAGATACAGGACGAAGAGGCAGCG
AGGCAGAAGGACGAGGAGATGAAGTCCAGGGGCATCCACGAGGACGACGACGTCCTGTTCAGCTACGACCCCGAC
ACTGACGGCGAAGAGCAACCCAAAGGAAACCCGGGGATCGACTACGACGAATACGACGAGACGGCGGAAGACGGC
GACGGCGAGGCGGCGGAGACCAAGGACGGCTTCGTGGATCGCATCTATCAAGAGATCTACGCCTCGCACCAGCGC
ATCACCTCTTCCGACCACAAGCCTGTCGTCTCCGTCTTCTCGCTCGACTACGATGCCGTCGTACCGGAGTTGAAG
GCCCAGGTCCACGCAGAGGTCGCTCGAGAGCTCGACCGGGCGGAGAACGAGGGCAGGCCGGGCATCACGATCGTC
GTCGAAGGCGACAAGGGACAACACGAGAGCGCCGTCGACTTTGGCGACCTCGCGTTTCTGGAGAGGAAGTCGTCT
ACCGTGACGATCGCAAATACCGGAGGTGTCTCCGCCAGCTTCTCGTTCGTGGAGCGGCCGACGACGGAGGACGGC
GAGCCGACGACGACTTCCTGGCTGACAACGTCCTTTGTCCGGACCGATGGTGACGCGACGGACCAGCTGGGCAAA
ACGGTGACACTCGAGCCCGGGGAGACGGTCTTGGCACACCTCGAGGCGCACGTTTTGGCCGCCGCTCAACTCCGG
GCGCTCAACGACGGCCAGCTCAAGCTCGAGGACATTCTGGTGTTGCGCGTCGAGGACGGGCGCGACCACTTCATC
CCCGTGCGCGCCGCCTGGCTTCCCACCTGCTTCGGCCGCTCCGTCGACGAGCTGATCCGCATTCCCGACGGGGGC
ATTCGAAAATTTGCGCGCGAAAAGGGCATCCAGGGAGCCATCTCGTACGACGCGGAGGTGCATCGCTCGGCGCCG
AAGGAGCTGTTCCAGCTGACGGAGGCGGTCCAGACGCTGGCCGAGCGGTGCGTAGCGGACGAGACGATGCTGGAA
GACATGGAGCTGCCTCGGGACCCAGGCTGGCCGCTCGAGCCGTCTTCGTGGACGGCCGGGGTGGCGGAGCAAAGC
TCGGTCAAGGGCGACATCGTCGCGGCCCTGGACACGGACAGGCCCATCTTCGAGGCGCTGCCGGTGGAAATGTCG
TCGGCCCACAAGCTCGAACTCGTGTCGGCGATCTTGCTGCTCTTCCTGACCTCGCTCACCGACGGCCTCGTCCCG
CCGCACCTGTGGGCCAAGCTATCCGCATCTCTCCCCAGCCTGACGGCGCTGCCTGCGGCGGCGTGGCCCGACATC
AGGTCTCAGGCGCTCGACATGCTGTCGACGGCGCCGAACCACAACATCGCCTTCATCTTCCTGACGGCCACGATG
TCGCGGGTGGCGGCCGAGCTCAGCCCCGGCACGGCGGAGGGATCCCGGCTGTCCGGGCTGGGCCGGCGGCTGAGC
TTCCGGAGAGGCGACGAGGACGGGTCGAAGAAGCGGCGGGCGCGGGAGAAGAAGTACGCCGAGGTGCTGGGGCCG
CTGACCTTCCGGGCCAACGATAAGGACAAGGCCATGAAGGACAAGGAGAGGCTCCTGCTCGAAATGTTTCTGAGT
CGAGAGGCGAGGAGCTAG
Transcript >Hirsu2|3446
ATGTCGGCCTCATCCAGCGCGTCGTCCTCGGGCTCCGTCGGCTCGGAGCCGGTGGACCTATCGACGACTCCGCAG
TCGCTGGCCAGGGCCGTCCTGGCCCGGCGCGGCGAATACGTGCGCCGGCGCAGCATGCGTGTCAAGATCGGCACC
TGGAACGTCGCCGCCTGCCCCGGCACCGACAAAGACCTGGCCAGCTGGTTCGTCGACGGTCGCGGCCTCGACAAG
AGCCTGGCTGCCGTCGACCTCTCCCGCAACCCGGCCGTCGACGGCAACGGCTCCGCCACGGCCGACGCCGGCTCC
GGCTCCGGCTCCGTTCGCCTGGTCGGCGGAGAAGACATCGGCCTCTACGTGCTGGGGCTGCAAGAGGTCGTCGAC
CTCAACGGGACGAGGGAATACATGAACCGCGCCGTCTACACCGACAACGGCCCGATGCAGAAGTGGCAGGCAGCG
GTCGAGGCCATGCTGCCTCCCGGGTACGAGCTCGTCGTCGCCGAGCAGATGACGGGCATCCTCCTCCTCGTCTAC
GCCTCTCCCGACGTCGCGCCCACCATCAGCAACGTGAGCACCAAGCAGGTCGGCACAGGGCTCCTTGGCTACTTT
GGAAACAAGGGCGCCGTCACCACCCGGCTCGTCCTGGGCGAGGCGACTCGCATCGTCCTCGTCAACTGCCATCTC
GCTAGTGGCGCCAACCCCAGCTACCTCGACCGGCGCTGCTGGGACGTCGGCCAGATTCTGGCCAAGACGCAGTTC
GAGCCCGTCGTGCACGGGGGCGTGGCCGAGGACGACGGCGACAAGGTCGGCGACGAGGACTTTGCTTTTTGGTTT
GGCGACCTCAACTTCCGCCTCGACGGCCTGCCGGGCGAAGACATAAGGAGGCTGCTGACGCTGCACACGCGCGGC
GAATACGACCTGAGCCAGGACCGGCCTCCTCTTCCGCTGGGCGGCGATCCGTTCATCGTCATGAAAAGCTGCGAG
AGCGACGATGACACGAGCACGATTCCCTCGACGCATTCGCGAGACCAGAGCTTCGACTCTAAGAGCTCGCTGCCC
GACCCCGACGATTTCCCCCAGGATGCAAGCCAGGATCCGACGTCCCTGCAGGCAACCCTGGACTCACTGCTGCCC
CACGACCAGCTGAGGCGCGTCATAGCCGAGCGCAAAGTCTTCCATGACGGCTGGAGGGAAGGCCACATCGGCTTC
CTCCCATCGTACAAGTACGACGTCGGCACCGTTGGCCTGTTCGATTCGAGCGAGAAGCAGCGCGCCCCCAGCTGG
TGCGATCGGATTCTCTTCCGAACCCGCAAGGACAAGAGGGGGTACGACAAGCAGATACAGGACGAAGAGGCAGCG
AGGCAGAAGGACGAGGAGATGAAGTCCAGGGGCATCCACGAGGACGACGACGTCCTGTTCAGCTACGACCCCGAC
ACTGACGGCGAAGAGCAACCCAAAGGAAACCCGGGGATCGACTACGACGAATACGACGAGACGGCGGAAGACGGC
GACGGCGAGGCGGCGGAGACCAAGGACGGCTTCGTGGATCGCATCTATCAAGAGATCTACGCCTCGCACCAGCGC
ATCACCTCTTCCGACCACAAGCCTGTCGTCTCCGTCTTCTCGCTCGACTACGATGCCGTCGTACCGGAGTTGAAG
GCCCAGGTCCACGCAGAGGTCGCTCGAGAGCTCGACCGGGCGGAGAACGAGGGCAGGCCGGGCATCACGATCGTC
GTCGAAGGCGACAAGGGACAACACGAGAGCGCCGTCGACTTTGGCGACCTCGCGTTTCTGGAGAGGAAGTCGTCT
ACCGTGACGATCGCAAATACCGGAGGTGTCTCCGCCAGCTTCTCGTTCGTGGAGCGGCCGACGACGGAGGACGGC
GAGCCGACGACGACTTCCTGGCTGACAACGTCCTTTGTCCGGACCGATGGTGACGCGACGGACCAGCTGGGCAAA
ACGGTGACACTCGAGCCCGGGGAGACGGTCTTGGCACACCTCGAGGCGCACGTTTTGGCCGCCGCTCAACTCCGG
GCGCTCAACGACGGCCAGCTCAAGCTCGAGGACATTCTGGTGTTGCGCGTCGAGGACGGGCGCGACCACTTCATC
CCCGTGCGCGCCGCCTGGCTTCCCACCTGCTTCGGCCGCTCCGTCGACGAGCTGATCCGCATTCCCGACGGGGGC
ATTCGAAAATTTGCGCGCGAAAAGGGCATCCAGGGAGCCATCTCGTACGACGCGGAGGTGCATCGCTCGGCGCCG
AAGGAGCTGTTCCAGCTGACGGAGGCGGTCCAGACGCTGGCCGAGCGGTGCGTAGCGGACGAGACGATGCTGGAA
GACATGGAGCTGCCTCGGGACCCAGGCTGGCCGCTCGAGCCGTCTTCGTGGACGGCCGGGGTGGCGGAGCAAAGC
TCGGTCAAGGGCGACATCGTCGCGGCCCTGGACACGGACAGGCCCATCTTCGAGGCGCTGCCGGTGGAAATGTCG
TCGGCCCACAAGCTCGAACTCGTGTCGGCGATCTTGCTGCTCTTCCTGACCTCGCTCACCGACGGCCTCGTCCCG
CCGCACCTGTGGGCCAAGCTATCCGCATCTCTCCCCAGCCTGACGGCGCTGCCTGCGGCGGCGTGGCCCGACATC
AGGTCTCAGGCGCTCGACATGCTGTCGACGGCGCCGAACCACAACATCGCCTTCATCTTCCTGACGGCCACGATG
TCGCGGGTGGCGGCCGAGCTCAGCCCCGGCACGGCGGAGGGATCCCGGCTGTCCGGGCTGGGCCGGCGGCTGAGC
TTCCGGAGAGGCGACGAGGACGGGTCGAAGAAGCGGCGGGCGCGGGAGAAGAAGTACGCCGAGGTGCTGGGGCCG
CTGACCTTCCGGGCCAACGATAAGGACAAGGCCATGAAGGACAAGGAGAGGCTCCTGCTCGAAATGTTTCTGAGT
CGAGAGGCGAGGAGCTAG
Gene >Hirsu2|3446
ATGTCGGCCTCATCCAGCGCGTCGTCCTCGGGCTCCGTCGGCTCGGAGCCGGTGGACCTATCGACGACTCCGCAG
TCGCTGGCCAGGGCCGTCCTGGCCCGGCGCGGCGAATACGTGCGCCGGCGCAGCATGCGTGTCAAGATCGGCACC
TGGAACGTCGCCGCCTGCCCCGGCACCGACAAAGACCTGGCCAGCTGGTTCGTCGACGGTCGCGGCCTCGACAAG
AGCCTGGCTGCCGTCGACCTCTCCCGCAACCCGGCCGTCGACGGCAACGGCTCCGCCACGGCCGACGCCGGCTCC
GGCTCCGGCTCCGTTCGCCTGGTCGGCGGAGAAGACATCGGCCTCTACGTGCTGGGGCTGCAAGAGGTCGTCGAC
CTCAACGGGACGAGGGAATACATGAACCGCGCCGTCTACACCGACAACGGCCCGATGCAGAAGTGGCAGGCAGCG
GTCGAGGCCATGCTGCCTCCCGGGTACGAGCTCGTCGTCGCCGAGCAGATGACGGGCATCCTCCTCCTCGTCTAC
GCCTCTCCCGACGTCGCGCCCACCATCAGCAACGTGAGCACCAAGCAGGTCGGCACAGGGCTCCTTGGCTACTTT
GGAAACAAGGGCGCCGTCACCACCCGGCTCGTCCTGGGCGAGGCGACTCGCATCGTCCTCGTCAACTGCCATCTC
GCTAGTGGCGCCAACCCCAGCTACCTCGACCGGCGCTGCTGGGACGTCGGCCAGATTCTGGCCAAGACGCAGTTC
GAGCCCGTCGTGCACGGGGGCGTGGCCGAGGACGACGGCGACAAGGTCGGCGACGAGGACTTTGCTTTTTGGTTT
GGCGACCTCAACTTCCGCCTCGACGGCCTGCCGGGCGAAGACATAAGGAGGCTGCTGACGCTGCACACGCGCGGC
GAATACGACCTGAGCCAGGACCGGCCTCCTCTTCCGCTGGGCGGCGATCCGTTCATCGTCATGAAAAGCTGCGAG
AGCGACGATGACACGAGCACGATTCCCTCGACGCATTCGCGAGACCAGAGCTTCGACTCTAAGAGCTCGCTGCCC
GACCCCGACGATTTCCCCCAGGATGCAAGCCAGGATCCGACGTCCCTGCAGGCAACCCTGGACTCACTGCTGCCC
CACGACCAGCTGAGGCGCGTCATAGCCGAGCGCAAAGTCTTCCATGACGGCTGGAGGGAAGGCCACATCGGCTTC
CTCCCATCGTACAAGTACGACGTCGGCACCGTTGGCCTGTTCGATTCGAGCGAGAAGCAGCGCGCCCCCAGCTGG
TGCGATCGGATTCTCTTCCGAACCCGCAAGGACAAGAGGGGGTACGACAAGCAGATACAGGACGAAGAGGCAGCG
AGGCAGAAGGACGAGGAGATGAAGTCCAGGGGCATCCACGAGGACGACGACGTCCTGTTCAGCTACGACCCCGAC
ACTGACGGCGAAGAGCAACCCAAAGGAAACCCGGGGATCGACTACGACGAATACGACGAGACGGCGGAAGACGGC
GACGGCGAGGCGGCGGAGACCAAGGACGGCTTCGTGGATCGCATCTATCAAGAGATCTACGCCTCGCACCAGCGC
ATCACCTCTTCCGACCACAAGCCTGTCGTCTCCGTCTTCTCGCTCGACTACGATGCCGTCGTACCGGAGTTGAAG
GCCCAGGTCCACGCAGAGGTCGCTCGAGAGCTCGACCGGGCGGAGAACGAGGGCAGGCCGGGCATCACGATCGTC
GTCGAAGGCGACAAGGGACAACACGAGAGCGCCGTCGACTTTGGCGACCTCGCGTTTCTGGAGAGGAAGTCGTCT
ACCGTGACGATCGCAAATACCGGAGGTGTCTCCGCCAGCTTCTCGTTCGTGGAGCGGCCGACGACGGAGGACGGC
GAGCCGACGACGACTTCCTGGCTGACAACGTCCTTTGTCCGGACCGATGGTGACGCGACGGACCAGCTGGGCAAA
ACGGTGACACTCGAGCCCGGGGAGACGGTCTTGGCACACCTCGAGGCGCACGTTTTGGCCGCCGCTCAACTCCGG
GCGCTCAACGACGGCCAGCTCAAGCTCGAGGACATTCTGGTGTTGCGCGTCGAGGACGGGCGCGACCACTTCATC
CCCGTGCGCGCCGCCTGGCTTCCCACCTGCTTCGGCCGCTCCGTCGACGAGCTGATCCGCATTCCCGACGGGGGC
ATTCGAAAATTTGCGCGCGAAAAGGGCATCCAGGGAGCCATCTCGTACGACGCGGAGGTGCATCGCTCGGCGCCG
AAGGAGCTGTTCCAGCTGACGGAGGCGGTCCAGACGCTGGCCGAGCGGTGCGTAGCGGACGAGACGATGCTGGAA
GACATGGAGCTGCCTCGGGACCCAGGCTGGCCGCTCGAGCCGTCTTCGTGGACGGCCGGGGTGGCGGAGCAAAGC
TCGGTCAAGGGCGACATCGTCGCGGCCCTGGACACGGACAGGCCCATCTTCGAGGCGCTGCCGGTGGAAATGTCG
TCGGCCCACAAGCTCGAACTCGTGTCGGCGATCTTGCTGCTCTTCCTGACCTCGCTCACCGACGGCCTCGTCCCG
CCGCACCTGTGGGCCAAGCTATCCGCATCTCTCCCCAGCCTGACGGCGCTGCCTGCGGCGGCGTGGCCCGACATC
AGGTCTCAGGCGCTCGACATGCTGTCGACGGCGCCGAACCACAACATCGCCTTCATCTTCCTGACGGCCACGATG
TCGCGGGTGGCGGCCGAGCTCAGCCCCGGCACGGCGGAGGGATCCCGGCTGTCCGGGCTGGGCCGGCGGCTGAGC
TTCCGGAGAGGCGACGAGGACGGGTCGAAGAAGCGGCGGGCGCGGGAGAAGAAGTACGCCGAGGTGCTGGGGCCG
CTGACCTTCCGGGCCAACGATAAGGACAAGGCCATGAAGGACAAGGAGAGGCTCCTGCTCGAAATGTTTCTGAGT
CGAGAGGCGAGGAGCTAG

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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