Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|2437
Gene name
LocationContig_1582:611..3583
Strand-
Gene length (bp)2972
Transcript length (bp)2829
Coding sequence length (bp)2829
Protein length (aa) 943

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF01822 WSC WSC domain 3.6E-17 613 688
PF01822 WSC WSC domain 6.7E-17 723 800
PF01822 WSC WSC domain 1.2E-14 830 906
PF00141 peroxidase Peroxidase 4.9E-21 56 230

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|D4AUF4|WSCD2_ARTBC WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 8 531 3.0E-131
sp|D4AUF4|WSCD2_ARTBC WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 713 916 5.0E-38
sp|D4AUF4|WSCD2_ARTBC WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 609 808 2.0E-37
sp|D4AUF1|WSCD1_ARTBC WSC domain-containing protein ARB_07867 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07867 PE=1 SV=1 603 915 7.0E-35
sp|P84675|PFM_CHAGB Putative fungistatic metabolite OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=CHGG_05463 PE=1 SV=2 610 808 9.0E-31
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Swissprot ID Swissprot Description Start End E-value
sp|D4AUF4|WSCD2_ARTBC WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 8 531 3.0E-131
sp|D4AUF4|WSCD2_ARTBC WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 713 916 5.0E-38
sp|D4AUF4|WSCD2_ARTBC WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 609 808 2.0E-37
sp|D4AUF1|WSCD1_ARTBC WSC domain-containing protein ARB_07867 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07867 PE=1 SV=1 603 915 7.0E-35
sp|P84675|PFM_CHAGB Putative fungistatic metabolite OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=CHGG_05463 PE=1 SV=2 610 808 9.0E-31
sp|P84675|PFM_CHAGB Putative fungistatic metabolite OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=CHGG_05463 PE=1 SV=2 715 915 1.0E-26
sp|D4AUF1|WSCD1_ARTBC WSC domain-containing protein ARB_07867 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07867 PE=1 SV=1 709 927 2.0E-22
sp|D4AUF4|WSCD2_ARTBC WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 826 928 3.0E-19
sp|D4AUF1|WSCD1_ARTBC WSC domain-containing protein ARB_07867 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07867 PE=1 SV=1 579 808 7.0E-18
sp|Q7XZP5|APX5_ARATH L-ascorbate peroxidase 5, peroxisomal OS=Arabidopsis thaliana GN=APX5 PE=1 SV=2 58 233 7.0E-18
sp|A2BGL3|WSCD2_DANRE WSC domain-containing protein 2 OS=Danio rerio GN=wscd2 PE=3 SV=1 612 808 9.0E-16
sp|Q2TBF2|WSCD2_HUMAN WSC domain-containing protein 2 OS=Homo sapiens GN=WSCD2 PE=2 SV=2 612 831 2.0E-15
sp|Q6ZJJ1|APX4_ORYSJ Probable L-ascorbate peroxidase 4 OS=Oryza sativa subsp. japonica GN=APX4 PE=2 SV=1 65 244 2.0E-15
sp|A2BGL3|WSCD2_DANRE WSC domain-containing protein 2 OS=Danio rerio GN=wscd2 PE=3 SV=1 723 915 6.0E-14
sp|D4PHA7|WSCD2_MOUSE WSC domain-containing protein 2 OS=Mus musculus GN=Wscd2 PE=2 SV=1 612 808 2.0E-13
sp|Q0IIY2|WSCD1_XENTR WSC domain-containing protein 1 OS=Xenopus tropicalis GN=wscd1 PE=2 SV=1 702 915 6.0E-13
sp|Q2TBF2|WSCD2_HUMAN WSC domain-containing protein 2 OS=Homo sapiens GN=WSCD2 PE=2 SV=2 723 915 7.0E-13
sp|Q42564|APX3_ARATH L-ascorbate peroxidase 3, peroxisomal OS=Arabidopsis thaliana GN=APX3 PE=1 SV=1 65 252 2.0E-12
sp|Q01MI9|APX3_ORYSI Probable L-ascorbate peroxidase 3 OS=Oryza sativa subsp. indica GN=APX3 PE=2 SV=1 65 244 2.0E-12
sp|Q0JEQ2|APX3_ORYSJ Probable L-ascorbate peroxidase 3 OS=Oryza sativa subsp. japonica GN=APX3 PE=3 SV=1 65 244 2.0E-12
sp|Q80XH4|WSCD1_MOUSE WSC domain-containing protein 1 OS=Mus musculus GN=Wscd1 PE=2 SV=1 595 772 1.0E-11
sp|D4AUF4|WSCD2_ARTBC WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 596 697 1.0E-11
sp|D4PHA7|WSCD2_MOUSE WSC domain-containing protein 2 OS=Mus musculus GN=Wscd2 PE=2 SV=1 723 915 1.0E-11
sp|Q8GY91|APX6_ARATH Putative L-ascorbate peroxidase 6 OS=Arabidopsis thaliana GN=APX6 PE=2 SV=1 60 191 2.0E-11
sp|Q658N2|WSCD1_HUMAN WSC domain-containing protein 1 OS=Homo sapiens GN=WSCD1 PE=2 SV=1 595 772 2.0E-11
sp|Q0IIY2|WSCD1_XENTR WSC domain-containing protein 1 OS=Xenopus tropicalis GN=wscd1 PE=2 SV=1 596 793 4.0E-11
sp|Q658N2|WSCD1_HUMAN WSC domain-containing protein 1 OS=Homo sapiens GN=WSCD1 PE=2 SV=1 721 878 4.0E-11
sp|A4R606|CCPR2_MAGO7 Putative heme-binding peroxidase OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=MGG_10368 PE=3 SV=1 65 194 5.0E-11
sp|Q6BKY9|CCPR_DEBHA Cytochrome c peroxidase, mitochondrial OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=CCP1 PE=3 SV=1 66 307 3.0E-10
sp|Q1PER6|APX2_ARATH L-ascorbate peroxidase 2, cytosolic OS=Arabidopsis thaliana GN=APX2 PE=2 SV=3 65 232 3.0E-10
sp|Q505J3|WSCD1_RAT WSC domain-containing protein 1 OS=Rattus norvegicus GN=Wscd1 PE=2 SV=1 612 772 3.0E-10
sp|P48534|APX1_PEA L-ascorbate peroxidase, cytosolic OS=Pisum sativum GN=APX1 PE=1 SV=2 65 252 3.0E-10
sp|Q10N21|APX1_ORYSJ L-ascorbate peroxidase 1, cytosolic OS=Oryza sativa subsp. japonica GN=APX1 PE=1 SV=1 65 237 3.0E-09
sp|A2XFC7|APX1_ORYSI L-ascorbate peroxidase 1, cytosolic OS=Oryza sativa subsp. indica GN=APX1 PE=2 SV=1 65 237 3.0E-09
sp|Q9FE01|APX2_ORYSJ L-ascorbate peroxidase 2, cytosolic OS=Oryza sativa subsp. japonica GN=APX2 PE=1 SV=1 65 237 1.0E-08
sp|Q42592|APXS_ARATH L-ascorbate peroxidase S, chloroplastic/mitochondrial OS=Arabidopsis thaliana GN=APXS PE=1 SV=2 40 254 1.0E-08
sp|Q80XH4|WSCD1_MOUSE WSC domain-containing protein 1 OS=Mus musculus GN=Wscd1 PE=2 SV=1 723 878 2.0E-08
sp|Q7XJ02|APX7_ORYSJ Probable L-ascorbate peroxidase 7, chloroplastic OS=Oryza sativa subsp. japonica GN=APX7 PE=2 SV=1 65 254 2.0E-08
sp|Q505J3|WSCD1_RAT WSC domain-containing protein 1 OS=Rattus norvegicus GN=Wscd1 PE=2 SV=1 723 878 2.0E-08
sp|Q9FL16|PER63_ARATH Peroxidase 63 OS=Arabidopsis thaliana GN=PER63 PE=2 SV=1 41 212 3.0E-08
sp|P84675|PFM_CHAGB Putative fungistatic metabolite OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=CHGG_05463 PE=1 SV=2 821 930 4.0E-08
sp|Q05431|APX1_ARATH L-ascorbate peroxidase 1, cytosolic OS=Arabidopsis thaliana GN=APX1 PE=1 SV=2 65 237 5.0E-08
sp|Q2TBF2|WSCD2_HUMAN WSC domain-containing protein 2 OS=Homo sapiens GN=WSCD2 PE=2 SV=2 797 919 7.0E-08
sp|Q4WLG9|CCPR2_ASPFU Putative heme-binding peroxidase OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=AFUA_6G13570 PE=3 SV=1 64 194 9.0E-08
sp|P0C0L1|APX6_ORYSJ Probable L-ascorbate peroxidase 6, chloroplastic OS=Oryza sativa subsp. japonica GN=APX6 PE=2 SV=1 65 267 9.0E-08
sp|A2BGL3|WSCD2_DANRE WSC domain-containing protein 2 OS=Danio rerio GN=wscd2 PE=3 SV=1 816 915 1.0E-07
sp|Q5QQ53|XYLT_DROPS Xylosyltransferase oxt OS=Drosophila pseudoobscura pseudoobscura GN=oxt PE=2 SV=1 612 710 1.0E-07
sp|Q6C7U1|CCPR3_YARLI Putative heme-binding peroxidase OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=YALI0D25366g PE=3 SV=1 65 223 1.0E-07
sp|Q42593|APXT_ARATH L-ascorbate peroxidase T, chloroplastic OS=Arabidopsis thaliana GN=APXT PE=2 SV=2 65 191 2.0E-07
sp|D4PHA7|WSCD2_MOUSE WSC domain-containing protein 2 OS=Mus musculus GN=Wscd2 PE=2 SV=1 831 919 4.0E-07
sp|Q4HWQ2|CCPR2_GIBZE Putative heme-binding peroxidase OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=FGSG_10606 PE=3 SV=1 65 194 4.0E-07
sp|Q69SV0|APX8_ORYSJ Probable L-ascorbate peroxidase 8, chloroplastic OS=Oryza sativa subsp. japonica GN=APX8 PE=2 SV=2 65 191 5.0E-07
sp|Q7KVA1|XYLT_DROME Xylosyltransferase oxt OS=Drosophila melanogaster GN=oxt PE=2 SV=1 612 710 6.0E-07
sp|Q6C0Z6|CCPR_YARLI Cytochrome c peroxidase, mitochondrial OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=CCP1 PE=3 SV=1 65 232 7.0E-07
sp|Q9UR19|VPL1_PLEER Versatile peroxidase VPL1 OS=Pleurotus eryngii GN=vpl1 PE=1 SV=1 59 232 8.0E-07
sp|P0C0V3|CCPR_EMENI Cytochrome c peroxidase, mitochondrial OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=ccp1 PE=3 SV=1 65 236 8.0E-07
sp|Q7SDV9|CCPR_NEUCR Cytochrome c peroxidase, mitochondrial OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=ccp-1 PE=3 SV=1 65 288 1.0E-06
sp|Q4PBY6|CCPR_USTMA Cytochrome c peroxidase, mitochondrial OS=Ustilago maydis (strain 521 / FGSC 9021) GN=CCP1 PE=3 SV=1 65 194 1.0E-06
sp|P19136|PEM4_PHACH Manganese peroxidase H4 OS=Phanerochaete chrysosporium PE=1 SV=1 59 236 1.0E-06
sp|O94753|VPL2_PLEER Versatile peroxidase VPL2 OS=Pleurotus eryngii GN=vpl2 PE=1 SV=1 59 232 2.0E-06
sp|Q5B1Z0|CCPR2_EMENI Putative heme-binding peroxidase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=AN5440 PE=3 SV=1 65 194 2.0E-06
sp|Q5AEN1|CCPR_CANAL Cytochrome c peroxidase, mitochondrial OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CCP1 PE=3 SV=1 65 195 2.0E-06
sp|A4QVH4|CCPR_MAGO7 Cytochrome c peroxidase, mitochondrial OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=CCP1 PE=3 SV=1 65 194 3.0E-06
sp|P00431|CCPR_YEAST Cytochrome c peroxidase, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CCP1 PE=1 SV=2 65 196 3.0E-06
sp|Q4PD66|CCPR2_USTMA Putative heme-binding peroxidase OS=Ustilago maydis (strain 521 / FGSC 9021) GN=CCP2 PE=3 SV=1 65 194 4.0E-06
sp|Q6FMG7|CCPR_CANGA Cytochrome c peroxidase, mitochondrial OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=CAGL0K08184g PE=3 SV=1 65 196 4.0E-06
sp|Q6CAB5|CCPR2_YARLI Putative cytochrome c peroxidase, mitochondrial OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=YALI0D04268g PE=3 SV=1 65 194 5.0E-06
sp|Q6BIB1|CCPR2_DEBHA Putative heme-binding peroxidase OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=DEHA2G12166g PE=3 SV=3 65 196 9.0E-06
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GO

GO Term Description Terminal node
GO:0006979 response to oxidative stress Yes
GO:0020037 heme binding Yes
GO:0004601 peroxidase activity Yes
GO:0006950 response to stress No
GO:0016491 oxidoreductase activity No
GO:0046906 tetrapyrrole binding No
GO:0003824 catalytic activity No
GO:0097159 organic cyclic compound binding No
GO:0005488 binding No
GO:1901363 heterocyclic compound binding No
GO:0016684 oxidoreductase activity, acting on peroxide as acceptor No
GO:0016209 antioxidant activity No
GO:0003674 molecular_function No
GO:0008150 biological_process No
GO:0050896 response to stimulus No

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
Extracellular Signal peptide 0.1383 0.1001 0.974 0.1366 0.1141 0.0163 0.065 0.1315 0.0911 0.0038

SignalP

SignalP signal predicted Location Score
Yes 1 - 16 0.992163

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

CAZyme category E-value Start End
AA2 1.2E-28 58 238

Secondary Metabolism

(None)

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup2086
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|1235
Ophiocordyceps australis map64 (Brazil) OphauB2|4163
Ophiocordyceps camponoti-floridani Ophcf2|04887
Ophiocordyceps camponoti-rufipedis Ophun1|5202
Ophiocordyceps kimflemingae Ophio5|2532
Ophiocordyceps subramaniannii Hirsu2|2437 (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|2437
MRSSSVLLALGGLALADPTWPSEVDELEEIMYQLHSFRGRKFADTVSPCSNEASGPGRQNAAEWLRTAFHDMSTA
NTFFNTGGLDGSLQYELDNGENTGPGHKTTLEFMAPYVSPKSSLADLIALGVYTSVRSCGGPAVPFRAGRKDAAG
RGNTGVPQPQNSAFTFKQQFERMGFSEKEMIQVTVCGHTLGGVHQKEFPELMVPGAKDGEAPSDSTPAVFDNKVA
TEYLSGKTNNPLVVGPSVRLNKNSDFKVFNADGNKTVEEMADPERFRAICRTVLQKMIDVVPPGVTLTDPVVPYA
VKPVDMQLTLAQGGDALSWTGYIRVRTTGLARDAVKSVSIDYKDRHGSASCGSSSCTVTSTIQGVSQGFDDQFGF
FPVQATIPAESGISSFTVTVHQADGTSKLYDNNGKGYPMQDDVLFLPPQSCVRGSTGALTVVAAVRNDVAGRGAT
ANVWYKEPQSNSPVPRLQNASFGLEKGRCAGRYTLFTSDYTVQGGLPYQSHVDVTVGGRTDGFKSLAGVGGTCAA
LENAAPCRAAPKTLSGRDVTTTTASAPAVVVPPTTAAATTTTAAVTPAPPPPPPTTTTTTTTTSASTAPPPAVTP
QHRAAVGGYTLVSCWTEGNNTRALSGISFANDTMTLEKCMDHCSAYVYWGTEYGRECYCGNSLSSSSQKAPLGEC
NMACGGNGSDYCGAGNRLELYSTTSAPATPTPTATLIHKPTVAPYTLVGCWTEGQGARALGQKATIDGKGMSNEA
CAAFCKEYKYFGTEYGSECYCGSYLAGGSQTAPLGECNMACAGDAYEYCGASSRLELYMNPNATGGRPEQPAAVG
DYVLAGCRTEGNGTRALPDRTTAAEDMTNAKCADFCKGAAYFGTEYGRECYCGGALDASSKEAPAGECGMLCGGN
AAEFCGASNRLSVYKKKAAIPPPPPPPPPPARRDARRGTVAV*
Coding >Hirsu2|2437
ATGCGCTCCTCGTCCGTGCTGCTGGCCCTCGGCGGCCTGGCGCTGGCCGACCCGACCTGGCCGTCCGAGGTGGAC
GAGCTCGAGGAGATCATGTACCAGCTCCACTCGTTCCGCGGCCGCAAGTTCGCCGACACCGTCAGCCCCTGCTCC
AACGAGGCCTCGGGCCCCGGCCGCCAGAACGCGGCCGAGTGGCTCCGGACCGCCTTCCACGACATGTCGACGGCC
AACACCTTCTTCAACACGGGCGGCCTCGACGGCTCGCTCCAGTACGAGCTCGACAACGGCGAGAACACGGGCCCG
GGCCACAAGACGACGCTCGAGTTCATGGCCCCCTACGTCTCGCCCAAGTCGAGCCTGGCCGACCTCATCGCCCTC
GGCGTCTACACCTCGGTCCGCTCCTGCGGCGGCCCCGCCGTGCCCTTCCGCGCCGGCCGCAAGGACGCCGCCGGC
AGGGGGAACACGGGCGTGCCCCAGCCGCAGAACTCGGCCTTCACCTTCAAGCAGCAGTTCGAGCGCATGGGCTTC
AGCGAGAAGGAGATGATCCAGGTCACCGTCTGCGGCCACACCCTCGGCGGCGTCCACCAGAAGGAGTTCCCCGAG
CTGATGGTGCCCGGGGCCAAGGACGGCGAGGCCCCGTCCGACTCGACCCCGGCCGTCTTCGACAACAAGGTCGCG
ACCGAGTACCTGTCGGGCAAGACCAACAACCCGCTCGTCGTCGGGCCGTCGGTCAGGCTCAACAAGAACTCCGAC
TTCAAGGTCTTCAACGCCGACGGCAACAAGACGGTCGAGGAGATGGCCGACCCCGAGCGGTTCCGGGCCATCTGC
AGGACGGTGCTGCAGAAGATGATCGACGTCGTGCCGCCCGGCGTGACGCTGACGGACCCCGTCGTCCCCTACGCC
GTCAAGCCCGTCGACATGCAGCTCACGCTGGCCCAGGGCGGCGACGCGCTGTCGTGGACGGGCTACATCCGCGTC
CGGACGACGGGCCTGGCCCGGGACGCCGTCAAGAGCGTCAGCATCGACTACAAGGACCGCCACGGGTCGGCCTCG
TGCGGGTCCAGCTCCTGCACCGTCACCAGCACCATCCAGGGCGTCAGCCAGGGCTTCGACGACCAGTTCGGCTTC
TTCCCCGTCCAGGCCACCATCCCGGCCGAGTCGGGCATCTCGTCCTTCACCGTGACGGTGCACCAGGCCGACGGC
ACGAGCAAGCTGTACGACAACAACGGCAAGGGCTACCCCATGCAGGACGACGTCCTCTTCCTGCCGCCGCAGAGC
TGCGTCCGGGGATCGACGGGCGCCCTCACCGTCGTCGCCGCCGTCCGCAACGACGTGGCCGGCCGCGGCGCCACG
GCCAACGTCTGGTACAAGGAGCCGCAGTCCAACAGCCCCGTGCCGCGGCTGCAGAACGCCAGCTTTGGCCTCGAG
AAGGGCAGGTGCGCCGGCCGGTACACGCTCTTCACCTCCGACTACACCGTCCAGGGCGGGCTCCCCTACCAGTCG
CACGTCGACGTGACCGTCGGCGGCCGCACCGACGGCTTCAAGAGCCTGGCCGGCGTCGGCGGCACGTGTGCCGCG
CTCGAAAACGCCGCGCCCTGCCGGGCCGCTCCCAAGACGCTGTCCGGCCGCGACGTGACGACGACGACGGCGTCG
GCGCCGGCGGTGGTGGTGCCCCCCACGACGGCGGCGGCGACGACGACGACGGCGGCCGTGACTCCGGCGCCGCCT
CCCCCTCCACCGACGACGACGACGACGACGACGACGACGAGTGCCTCGACGGCACCGCCGCCGGCCGTGACGCCG
CAGCACCGGGCTGCCGTGGGCGGATACACGCTGGTGTCGTGCTGGACCGAGGGCAACAACACACGCGCCCTGTCG
GGCATCTCGTTTGCCAACGACACGATGACGCTGGAGAAGTGCATGGATCACTGCAGCGCGTACGTGTACTGGGGA
ACCGAGTACGGCCGAGAATGCTACTGCGGCAACTCGCTGTCGTCGAGCAGCCAGAAGGCGCCGCTGGGCGAGTGC
AACATGGCGTGCGGCGGCAACGGCAGCGACTACTGCGGAGCGGGCAACCGGCTGGAGCTGTACTCGACGACGTCG
GCGCCGGCGACGCCGACGCCGACGGCGACGCTGATCCACAAGCCGACGGTGGCGCCGTACACGCTGGTCGGGTGC
TGGACCGAGGGCCAGGGGGCGCGGGCGCTGGGGCAGAAGGCGACGATCGACGGCAAGGGCATGAGCAACGAGGCG
TGCGCGGCCTTCTGCAAGGAGTACAAGTACTTCGGGACCGAGTACGGCAGCGAGTGCTACTGCGGCAGCTACCTG
GCCGGGGGCAGCCAGACGGCGCCGCTGGGCGAGTGCAACATGGCGTGCGCGGGCGACGCGTACGAGTACTGCGGG
GCCAGCAGCCGGCTGGAGCTGTACATGAACCCGAACGCGACGGGCGGGCGGCCGGAGCAGCCGGCGGCGGTGGGC
GACTACGTGCTGGCCGGGTGCCGGACCGAGGGCAACGGGACGCGGGCGCTGCCGGACCGGACGACGGCGGCCGAG
GACATGACCAACGCCAAGTGCGCCGACTTCTGCAAGGGGGCGGCCTACTTCGGGACCGAGTACGGGCGCGAGTGC
TACTGCGGCGGCGCGCTCGACGCGTCGAGCAAGGAGGCGCCGGCGGGCGAGTGCGGCATGCTGTGCGGCGGCAAC
GCGGCCGAGTTCTGCGGCGCCTCGAACCGGCTGTCGGTGTACAAGAAGAAGGCGGCGATTCCTCCGCCGCCGCCG
CCGCCGCCGCCGCCGGCCAGGCGCGACGCCCGCCGGGGCACGGTAGCGGTGTGA
Transcript >Hirsu2|2437
ATGCGCTCCTCGTCCGTGCTGCTGGCCCTCGGCGGCCTGGCGCTGGCCGACCCGACCTGGCCGTCCGAGGTGGAC
GAGCTCGAGGAGATCATGTACCAGCTCCACTCGTTCCGCGGCCGCAAGTTCGCCGACACCGTCAGCCCCTGCTCC
AACGAGGCCTCGGGCCCCGGCCGCCAGAACGCGGCCGAGTGGCTCCGGACCGCCTTCCACGACATGTCGACGGCC
AACACCTTCTTCAACACGGGCGGCCTCGACGGCTCGCTCCAGTACGAGCTCGACAACGGCGAGAACACGGGCCCG
GGCCACAAGACGACGCTCGAGTTCATGGCCCCCTACGTCTCGCCCAAGTCGAGCCTGGCCGACCTCATCGCCCTC
GGCGTCTACACCTCGGTCCGCTCCTGCGGCGGCCCCGCCGTGCCCTTCCGCGCCGGCCGCAAGGACGCCGCCGGC
AGGGGGAACACGGGCGTGCCCCAGCCGCAGAACTCGGCCTTCACCTTCAAGCAGCAGTTCGAGCGCATGGGCTTC
AGCGAGAAGGAGATGATCCAGGTCACCGTCTGCGGCCACACCCTCGGCGGCGTCCACCAGAAGGAGTTCCCCGAG
CTGATGGTGCCCGGGGCCAAGGACGGCGAGGCCCCGTCCGACTCGACCCCGGCCGTCTTCGACAACAAGGTCGCG
ACCGAGTACCTGTCGGGCAAGACCAACAACCCGCTCGTCGTCGGGCCGTCGGTCAGGCTCAACAAGAACTCCGAC
TTCAAGGTCTTCAACGCCGACGGCAACAAGACGGTCGAGGAGATGGCCGACCCCGAGCGGTTCCGGGCCATCTGC
AGGACGGTGCTGCAGAAGATGATCGACGTCGTGCCGCCCGGCGTGACGCTGACGGACCCCGTCGTCCCCTACGCC
GTCAAGCCCGTCGACATGCAGCTCACGCTGGCCCAGGGCGGCGACGCGCTGTCGTGGACGGGCTACATCCGCGTC
CGGACGACGGGCCTGGCCCGGGACGCCGTCAAGAGCGTCAGCATCGACTACAAGGACCGCCACGGGTCGGCCTCG
TGCGGGTCCAGCTCCTGCACCGTCACCAGCACCATCCAGGGCGTCAGCCAGGGCTTCGACGACCAGTTCGGCTTC
TTCCCCGTCCAGGCCACCATCCCGGCCGAGTCGGGCATCTCGTCCTTCACCGTGACGGTGCACCAGGCCGACGGC
ACGAGCAAGCTGTACGACAACAACGGCAAGGGCTACCCCATGCAGGACGACGTCCTCTTCCTGCCGCCGCAGAGC
TGCGTCCGGGGATCGACGGGCGCCCTCACCGTCGTCGCCGCCGTCCGCAACGACGTGGCCGGCCGCGGCGCCACG
GCCAACGTCTGGTACAAGGAGCCGCAGTCCAACAGCCCCGTGCCGCGGCTGCAGAACGCCAGCTTTGGCCTCGAG
AAGGGCAGGTGCGCCGGCCGGTACACGCTCTTCACCTCCGACTACACCGTCCAGGGCGGGCTCCCCTACCAGTCG
CACGTCGACGTGACCGTCGGCGGCCGCACCGACGGCTTCAAGAGCCTGGCCGGCGTCGGCGGCACGTGTGCCGCG
CTCGAAAACGCCGCGCCCTGCCGGGCCGCTCCCAAGACGCTGTCCGGCCGCGACGTGACGACGACGACGGCGTCG
GCGCCGGCGGTGGTGGTGCCCCCCACGACGGCGGCGGCGACGACGACGACGGCGGCCGTGACTCCGGCGCCGCCT
CCCCCTCCACCGACGACGACGACGACGACGACGACGACGAGTGCCTCGACGGCACCGCCGCCGGCCGTGACGCCG
CAGCACCGGGCTGCCGTGGGCGGATACACGCTGGTGTCGTGCTGGACCGAGGGCAACAACACACGCGCCCTGTCG
GGCATCTCGTTTGCCAACGACACGATGACGCTGGAGAAGTGCATGGATCACTGCAGCGCGTACGTGTACTGGGGA
ACCGAGTACGGCCGAGAATGCTACTGCGGCAACTCGCTGTCGTCGAGCAGCCAGAAGGCGCCGCTGGGCGAGTGC
AACATGGCGTGCGGCGGCAACGGCAGCGACTACTGCGGAGCGGGCAACCGGCTGGAGCTGTACTCGACGACGTCG
GCGCCGGCGACGCCGACGCCGACGGCGACGCTGATCCACAAGCCGACGGTGGCGCCGTACACGCTGGTCGGGTGC
TGGACCGAGGGCCAGGGGGCGCGGGCGCTGGGGCAGAAGGCGACGATCGACGGCAAGGGCATGAGCAACGAGGCG
TGCGCGGCCTTCTGCAAGGAGTACAAGTACTTCGGGACCGAGTACGGCAGCGAGTGCTACTGCGGCAGCTACCTG
GCCGGGGGCAGCCAGACGGCGCCGCTGGGCGAGTGCAACATGGCGTGCGCGGGCGACGCGTACGAGTACTGCGGG
GCCAGCAGCCGGCTGGAGCTGTACATGAACCCGAACGCGACGGGCGGGCGGCCGGAGCAGCCGGCGGCGGTGGGC
GACTACGTGCTGGCCGGGTGCCGGACCGAGGGCAACGGGACGCGGGCGCTGCCGGACCGGACGACGGCGGCCGAG
GACATGACCAACGCCAAGTGCGCCGACTTCTGCAAGGGGGCGGCCTACTTCGGGACCGAGTACGGGCGCGAGTGC
TACTGCGGCGGCGCGCTCGACGCGTCGAGCAAGGAGGCGCCGGCGGGCGAGTGCGGCATGCTGTGCGGCGGCAAC
GCGGCCGAGTTCTGCGGCGCCTCGAACCGGCTGTCGGTGTACAAGAAGAAGGCGGCGATTCCTCCGCCGCCGCCG
CCGCCGCCGCCGCCGGCCAGGCGCGACGCCCGCCGGGGCACGGTAGCGGTGTGA
Gene >Hirsu2|2437
ATGCGCTCCTCGTCCGTGCTGCTGGCCCTCGGCGGCCTGGCGCTGGCCGACCCGACCTGGCCGTCCGAGGTGGAC
GAGCTCGAGGAGATCATGTACCAGCTCCACTCGTTCCGCGGCCGCAAGTTCGCCGACACCGTCAGCCCCTGCTCC
AACGAGGCCTCGGGCCCCGGCCGCCAGAACGCGGCCGAGTGGCTCCGGACCGCCTTCCACGACATGTCGACGGCC
AACACCTTCTTCAACACGGGCGGCCTCGACGGCTCGCTCCAGTACGAGCTCGACAACGGCGAGAACACGGGCCCG
GGCCACAAGACGACGCTCGAGTTCATGGCCCCCTACGTCTCGCCCAAGTCGAGCCTGGCCGACCTCATCGCCCTC
GGCGTCTACACCTCGGTCCGCTCCTGCGGCGGCCCCGCCGTGCCCTTCCGCGCCGGCCGCAAGGACGCCGCCGGC
AGGGGGAACACGGGCGTGCCCCAGCCGCAGAACTCGGCCTTCACCTTCAAGCAGCAGTTCGAGCGCATGGGCTTC
AGCGAGAAGGAGATGATCCAGGTCACCGTCTGCGGCCACACCCTCGGCGGCGTCCACCAGAAGGAGTTCCCCGAG
CTGATGGTGCCCGGGGCCAAGGACGGCGAGGCCCCGTCCGACTCGACCCCGGCCGTCTTCGACAACAAGGTCGCG
ACCGAGTACCTGTCGGGCAAGACCAACAACCCGCTCGTCGTCGGGCCGTCGGTCAGGCTCAACAAGAACTCCGAC
TTCAAGGTCTTCAACGCCGACGGCAACAAGACGGTCGAGGAGATGGCCGACCCCGAGCGGTTCCGGGCCATCTGC
AGGACGGTGCTGCAGAAGATGATCGACGTCGTGCCGCCCGGCGTGACGCTGACGGACCCCGTCGTCCCCTACGCC
GTCAAGCCCGTCGACATGCAGCTCACGCTGGCCCAGGGCGGCGACGCGCTGTCGTGGACGGGCTACATCCGCGTC
CGGACGACGGGCCTGGCCCGGGACGCCGTCAAGAGCGTCAGCATCGACTACAAGGACCGCCACGGGTCGGCCTCG
TGCGGGTCCAGCTCCTGCACCGTCACCAGCACCATCCAGGGCGTCAGCCAGGGCTTCGACGACCAGTTCGGCTTC
TTCCCCGTCCAGGCCACCATCCCGGCCGAGTCGGGCATCTCGTCCTTCACCGTGACGGTGCACCAGGCCGACGGC
ACGAGCAAGCTGTACGACAACAACGGCAAGGGCTACCCCATGCAGGACGACGTCCTCTTCCTGCCGCCGCAGAGC
TGCGTCCGGGGATCGACGGGCGCCCTCACCGTCGTCGCCGCCGTCCGCAACGACGTGGCCGGCCGCGGCGCCACG
GCCAACGTCTGGTACAAGGAGCCGCAGTCCAACAGCCCCGTGCCGCGGCTGCAGAACGCCAGCTTTGGCCTCGAG
AAGGGCAGGTGCGCCGGCCGGTACACGCTCTTCACCTCCGACTACACCGTCCAGGGCGGGCTCCCCTACCAGTCG
CACGTCGACGTGACCGTCGGCGGCCGCACCGACGGCTTCAAGAGCCTGGCCGGCGTCGGCGGCACGTGTGCCGCG
CTCGAAAACGCCGCGCCCTGCCGGGCCGCTCCCAAGACGCTGTCCGGCCGCGACGTGACGACGACGACGGCGTCG
GCGCCGGCGGTGGTGGTGCCCCCCACGACGGCGGCGGCGACGACGACGACGGCGGCCGTGACTCCGGCGCCGCCT
CCCCCTCCACCGACGACGACGACGACGACGACGACGACGAGTGCCTCGACGGCACCGCCGCCGGCCGTGACGCCG
CAGCACCGGGCTGCCGTGGGCGGATACACGCTGGTGTCGTGCTGGACCGAGGGCAACAACACACGCGCCCTGTCG
GGCATCTCGTTTGCCAACGACACGATGACGCTGGAGAAGTGCATGGATCACTGCAGCGCGTACGTGTACTGGGGA
ACCGAGTACGGCCGAGAATGTACGTTTTTTTTTCCCACGTCTTTCTATCTACCCTCTCTCTCCCTCTCTCCCTAG
TCGTCAAGTTTCCCCCCTACCCTGTCCGGAATGGTGCCGGACGTCGTGACGAGAGGAAAGCGAGCGAGCTGACGA
GGACGGCGGCAGGCTACTGCGGCAACTCGCTGTCGTCGAGCAGCCAGAAGGCGCCGCTGGGCGAGTGCAACATGG
CGTGCGGCGGCAACGGCAGCGACTACTGCGGAGCGGGCAACCGGCTGGAGCTGTACTCGACGACGTCGGCGCCGG
CGACGCCGACGCCGACGGCGACGCTGATCCACAAGCCGACGGTGGCGCCGTACACGCTGGTCGGGTGCTGGACCG
AGGGCCAGGGGGCGCGGGCGCTGGGGCAGAAGGCGACGATCGACGGCAAGGGCATGAGCAACGAGGCGTGCGCGG
CCTTCTGCAAGGAGTACAAGTACTTCGGGACCGAGTACGGCAGCGAGTGCTACTGCGGCAGCTACCTGGCCGGGG
GCAGCCAGACGGCGCCGCTGGGCGAGTGCAACATGGCGTGCGCGGGCGACGCGTACGAGTACTGCGGGGCCAGCA
GCCGGCTGGAGCTGTACATGAACCCGAACGCGACGGGCGGGCGGCCGGAGCAGCCGGCGGCGGTGGGCGACTACG
TGCTGGCCGGGTGCCGGACCGAGGGCAACGGGACGCGGGCGCTGCCGGACCGGACGACGGCGGCCGAGGACATGA
CCAACGCCAAGTGCGCCGACTTCTGCAAGGGGGCGGCCTACTTCGGGACCGAGTACGGGCGCGAGTGCTACTGCG
GCGGCGCGCTCGACGCGTCGAGCAAGGAGGCGCCGGCGGGCGAGTGCGGCATGCTGTGCGGCGGCAACGCGGCCG
AGTTCTGCGGCGCCTCGAACCGGCTGTCGGTGTACAAGAAGAAGGCGGCGATTCCTCCGCCGCCGCCGCCGCCGC
CGCCGCCGGCCAGGCGCGACGCCCGCCGGGGCACGGTAGCGGTGTGA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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