Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|3631
Gene name
LocationContig_197:463..2680
Strand+
Gene length (bp)2217
Transcript length (bp)1761
Coding sequence length (bp)1761
Protein length (aa) 587

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00743 FMO-like Flavin-binding monooxygenase-like 4.1E-11 61 250
PF07992 Pyr_redox_2 Pyridine nucleotide-disulphide oxidoreductase 6.0E-11 59 263
PF13450 NAD_binding_8 NAD(P)-binding Rossmann-like domain 3.6E-07 61 107
PF13738 Pyr_redox_3 Pyridine nucleotide-disulphide oxidoreductase 6.5E-08 60 243
PF13434 Lys_Orn_oxgnase L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase 6.8E-07 126 260

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|A7HU16|BVMO_PARL1 Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 40 584 1.0E-162
sp|Q8GAW0|CPMO_COMS9 Cyclopentanone 1,2-monooxygenase OS=Comamonas sp. (strain NCIMB 9872) GN=cpnB PE=1 SV=3 50 576 7.0E-143
sp|P12015|CHMO_ACISP Cyclohexanone 1,2-monooxygenase OS=Acinetobacter sp. PE=1 SV=2 55 586 6.0E-107
sp|Q47PU3|PAMO_THEFY Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 56 567 7.0E-106
sp|A3U3H1|BVMO_OCEBH Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 53 576 2.0E-102
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Swissprot ID Swissprot Description Start End E-value
sp|A7HU16|BVMO_PARL1 Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 40 584 1.0E-162
sp|Q8GAW0|CPMO_COMS9 Cyclopentanone 1,2-monooxygenase OS=Comamonas sp. (strain NCIMB 9872) GN=cpnB PE=1 SV=3 50 576 7.0E-143
sp|P12015|CHMO_ACISP Cyclohexanone 1,2-monooxygenase OS=Acinetobacter sp. PE=1 SV=2 55 586 6.0E-107
sp|Q47PU3|PAMO_THEFY Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 56 567 7.0E-106
sp|A3U3H1|BVMO_OCEBH Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 53 576 2.0E-102
sp|H3JQW0|OTEMO_PSEPU 2-oxo-Delta(3)-4,5,5-trimethylcyclopentenylacetyl-CoA monooxygenase OS=Pseudomonas putida GN=otemo PE=1 SV=1 49 583 2.0E-95
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 61 540 2.0E-42
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 61 540 2.0E-42
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 61 540 2.0E-42
sp|E3VWK3|PENE_STREX Pentalenolactone D synthase OS=Streptomyces exfoliatus GN=penE PE=1 SV=1 56 550 1.0E-39
sp|Q9RKB5|BVMO2_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 61 540 5.0E-39
sp|E3VWI7|PNTE_STRAE Pentalenolactone D synthase OS=Streptomyces arenae GN=pntE PE=1 SV=1 56 550 3.0E-38
sp|Q9RL17|BVMO1_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO0300 PE=1 SV=1 75 579 9.0E-37
sp|U5S003|BVMO4_DIESD Baeyer-Villiger monooxygenase 4 OS=Dietzia sp. (strain D5) PE=1 SV=1 83 531 3.0E-36
sp|A1CLY7|CCSB_ASPCL Ketocytochalasin monooxygenase OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=ccsB PE=1 SV=1 40 477 2.0E-35
sp|Q9I3H5|BVMO_PSEAE Baeyer-Villiger monooxygenase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=PA1538 PE=1 SV=1 41 518 4.0E-34
sp|Q82IY8|PTLE_STRAW Neopentalenolactone D synthase OS=Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) GN=ptlE PE=1 SV=1 82 584 3.0E-33
sp|P55487|Y4ID_RHISN Uncharacterized monooxygenase y4iD OS=Rhizobium sp. (strain NGR234) GN=NGR_a03290 PE=3 SV=1 29 538 9.0E-32
sp|Q00730|STCW_EMENI Putative sterigmatocystin biosynthesis monooxygenase stcW OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=stcW PE=3 SV=2 57 585 6.0E-28
sp|Q93TJ5|HAPMO_PSEFL 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 56 263 7.0E-26
sp|P9WNF9|ETHA_MYCTU FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ethA PE=1 SV=1 57 479 3.0E-22
sp|P9WNF8|ETHA_MYCTO FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ethA PE=3 SV=1 57 479 3.0E-22
sp|Q7TVI2|ETHA_MYCBO FAD-containing monooxygenase EthA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ethA PE=1 SV=1 57 479 3.0E-22
sp|A0R665|ETHA_MYCS2 FAD-containing monooxygenase EthA OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=ethA PE=3 SV=1 57 479 4.0E-20
sp|P9WNF7|MYMA_MYCTU Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mymA PE=1 SV=1 57 524 3.0E-19
sp|P9WNF6|MYMA_MYCTO Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=mymA PE=3 SV=1 57 524 3.0E-19
sp|Q88J44|BVMO_PSEPK Baeyer-Villiger monooxygenase OS=Pseudomonas putida (strain KT2440) GN=PP_2805 PE=1 SV=1 48 262 1.0E-16
sp|Q9SVQ1|YUC2_ARATH Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 60 262 1.0E-12
sp|Q9LFM5|YUC4_ARATH Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 60 240 2.0E-12
sp|Q9SZY8|YUC1_ARATH Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 60 240 3.0E-12
sp|Q01740|FMO1_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 61 257 3.0E-12
sp|Q9SVU0|YUC8_ARATH Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 60 240 3.0E-11
sp|P16549|FMO1_PIG Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 61 257 7.0E-11
sp|Q95LA2|FMO1_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 61 266 2.0E-10
sp|P17636|FMO1_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 61 257 3.0E-10
sp|O64489|YUC9_ARATH Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 60 240 8.0E-10
sp|Q95LA1|FMO3_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 61 257 4.0E-09
sp|O23024|YUC3_ARATH Probable indole-3-pyruvate monooxygenase YUCCA3 OS=Arabidopsis thaliana GN=YUC3 PE=2 SV=1 60 240 5.0E-09
sp|P50285|FMO1_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 61 257 8.0E-09
sp|Q9LKC0|YUC5_ARATH Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 60 240 9.0E-09
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 61 251 1.0E-08
sp|P36365|FMO1_RAT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 61 257 1.0E-08
sp|Q8HYJ9|FMO3_BOVIN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 61 257 2.0E-08
sp|P97501|FMO3_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 61 257 4.0E-08
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 61 256 4.0E-08
sp|Q8K4B7|FMO4_RAT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 61 237 5.0E-08
sp|Q8SPQ7|FMO3_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 61 257 5.0E-08
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 61 256 7.0E-08
sp|P36366|FMO2_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 61 276 8.0E-08
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 61 256 8.0E-08
sp|Q99518|FMO2_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 61 256 9.0E-08
sp|O49312|YUC7_ARATH Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 60 240 9.0E-08
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 61 256 1.0E-07
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 61 251 1.0E-07
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 61 256 2.0E-07
sp|Q9EQ76|FMO3_RAT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 61 257 2.0E-07
sp|P31512|FMO4_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 61 257 2.0E-07
sp|Q5REK0|FMO2_PONAB Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 61 256 3.0E-07
sp|Q8VHG0|FMO4_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 61 257 3.0E-07
sp|P31513|FMO3_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 61 257 4.0E-07
sp|Q7YS44|FMO3_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 61 257 4.0E-07
sp|P32417|FMO3_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 61 257 5.0E-07
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 59 256 1.0E-06
sp|Q93TJ5|HAPMO_PSEFL 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 404 507 2.0E-06
sp|Q9FKE7|FMO2_ARATH Putative flavin-containing monooxygenase 2 OS=Arabidopsis thaliana GN=FMO2 PE=3 SV=2 61 299 5.0E-06
sp|P64766|Y968_MYCBO Uncharacterized protein Mb0968c OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0968c PE=4 SV=1 405 508 8.0E-06
sp|P9WKN7|Y943_MYCTU Uncharacterized protein Rv0943c OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0943c PE=4 SV=1 405 508 8.0E-06
sp|P9WKN6|Y943_MYCTO Uncharacterized protein MT0969 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0969 PE=4 SV=1 405 508 8.0E-06
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GO

GO Term Description Terminal node
GO:0016491 oxidoreductase activity Yes
GO:0004499 N,N-dimethylaniline monooxygenase activity Yes
GO:0050661 NADP binding Yes
GO:0050660 flavin adenine dinucleotide binding Yes
GO:0003674 molecular_function No
GO:0036094 small molecule binding No
GO:0043167 ion binding No
GO:1901363 heterocyclic compound binding No
GO:0005488 binding No
GO:0097159 organic cyclic compound binding No
GO:0003824 catalytic activity No
GO:0016709 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen No
GO:0000166 nucleotide binding No
GO:1901265 nucleoside phosphate binding No
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen No
GO:0004497 monooxygenase activity No
GO:0043168 anion binding 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
Cytoplasm 0.695 0.3322 0.3618 0.1006 0.0616 0.0352 0.0172 0.0829 0.0559 0.0299

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
Orthogroup418
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|1203
Ophiocordyceps australis 1348a (Ghana) OphauG2|5874
Ophiocordyceps australis map64 (Brazil) OphauB2|78
Ophiocordyceps camponoti-floridani Ophcf2|00015
Ophiocordyceps camponoti-rufipedis Ophun1|2799
Ophiocordyceps kimflemingae Ophio5|1784
Ophiocordyceps kimflemingae Ophio5|4092
Ophiocordyceps subramaniannii Hirsu2|3631 (this protein)
Ophiocordyceps subramaniannii Hirsu2|7961

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|3631
MNGGSASQNGGGQNGGPVPQNGGGQNGGPPPPSVRLRRELRSSSCAANSDSAVDVDLDALVVGAGFAGVFMLKTL
RERGLRVRIYEAGTDLGGTWRWNSYPGAAVDSETPEYEFSWPEVWKSWNWTTNYPQFKELRAYFDHVDKVLHIKK
DCSFNTVVTGAEFDIQMGRWRVRTDDGRLTTAKYLILGTGFSAKRYVPEWPGINDFKGIIHHSSFWPDENIAVGG
KKCAVIGTGASGVQIVQAWGPEAKELKVFQRTPNLAVPMRRRQLTAEDQEPGKKWYGELFRFREKTFGGFLYDWY
EKNTFDETAEQRQACYEEAWKAGGFRFWLSIYKDNLFNAEANRESYRFWAEKTRERIDDDRNKDLLAPLEMPHFF
GIKRPCLEHDYYEQFNRPSVHVLDIKDDPIERFTETGITLRSGAHHDFDVVAVATGFDVVTGAMTQLGLKSIDNQ
MLEEQWATGANTYLGVSVSGYPNMFHMYGAHGPTLLSNGPPCIEIQGRWIADCIEKMELNKIKVLNPKPEASVAW
KKQINQLYSTTLFPTTQSTYMGGSIPGKVSEPICFGGGLPAYATALRSALESMDGFEIEYE*
Coding >Hirsu2|3631
ATGAACGGCGGGTCGGCATCGCAGAACGGCGGGGGACAGAACGGAGGGCCGGTGCCGCAGAACGGCGGGGGACAG
AACGGCGGACCACCGCCGCCGAGCGTCCGGCTTCGCAGGGAGCTGCGCAGCTCTTCGTGCGCCGCCAACTCTGAC
TCCGCCGTCGACGTTGACCTCGATGCCCTCGTTGTCGGGGCCGGCTTCGCCGGCGTCTTCATGCTCAAGACGCTG
CGGGAGCGCGGCCTCCGCGTCCGCATCTACGAGGCCGGTACCGACCTCGGCGGCACCTGGCGCTGGAACTCATAT
CCTGGCGCGGCCGTCGACAGCGAGACGCCCGAGTACGAGTTCTCCTGGCCCGAGGTTTGGAAGAGCTGGAACTGG
ACGACCAACTATCCGCAGTTCAAGGAGCTCCGGGCCTACTTCGACCACGTCGACAAGGTGCTTCACATCAAGAAG
GACTGCTCCTTCAACACCGTCGTCACCGGCGCCGAGTTTGACATCCAAATGGGCCGCTGGAGGGTCCGGACTGAC
GACGGGAGACTCACGACGGCAAAGTATCTGATCTTGGGAACCGGCTTCTCCGCCAAGCGATATGTGCCGGAATGG
CCCGGGATCAACGACTTCAAGGGCATCATCCACCACTCATCCTTCTGGCCGGACGAGAACATCGCTGTCGGCGGC
AAGAAGTGCGCCGTCATCGGCACCGGCGCCTCCGGCGTGCAAATTGTCCAGGCCTGGGGCCCCGAGGCCAAGGAA
TTGAAAGTCTTCCAACGGACTCCCAACCTCGCCGTTCCCATGCGCCGGCGCCAGCTCACGGCCGAGGATCAGGAG
CCGGGCAAGAAGTGGTACGGCGAGCTGTTTAGGTTCCGCGAAAAGACCTTTGGCGGCTTCCTGTACGACTGGTAC
GAGAAGAACACCTTCGACGAGACGGCCGAGCAGCGGCAGGCTTGCTACGAGGAGGCCTGGAAGGCCGGTGGCTTC
CGCTTCTGGCTAAGCATCTACAAGGACAACCTGTTCAACGCCGAGGCCAACCGGGAGTCCTATCGATTCTGGGCC
GAAAAGACGCGCGAAAGGATCGACGACGACCGCAACAAGGACCTGCTCGCCCCCTTGGAGATGCCTCACTTCTTC
GGAATTAAAAGGCCGTGCCTCGAACACGACTACTACGAGCAGTTCAACCGTCCGTCGGTCCATGTCCTCGACATC
AAGGACGACCCGATCGAACGGTTTACTGAGACCGGAATCACCCTCAGGAGCGGAGCACACCATGACTTCGACGTC
GTGGCCGTTGCCACAGGTTTCGACGTTGTTACAGGAGCCATGACCCAGCTGGGCCTGAAGAGCATCGACAACCAG
ATGCTGGAAGAGCAGTGGGCGACTGGGGCGAACACCTACCTAGGGGTCAGCGTCAGCGGCTATCCCAACATGTTC
CACATGTACGGCGCCCACGGGCCGACGCTGCTGAGCAACGGGCCGCCCTGCATCGAAATTCAGGGCCGCTGGATC
GCCGACTGCATCGAAAAGATGGAGCTCAACAAAATCAAGGTCCTGAACCCAAAACCGGAGGCCTCGGTCGCGTGG
AAAAAGCAAATCAATCAGCTCTACAGCACCACCCTCTTCCCGACAACACAGTCGACCTACATGGGCGGCTCCATA
CCCGGCAAAGTCTCCGAGCCCATCTGCTTCGGCGGCGGACTGCCTGCGTACGCAACCGCGCTTCGGTCTGCTCTC
GAAAGCATGGACGGTTTCGAGATCGAGTACGAGTGA
Transcript >Hirsu2|3631
ATGAACGGCGGGTCGGCATCGCAGAACGGCGGGGGACAGAACGGAGGGCCGGTGCCGCAGAACGGCGGGGGACAG
AACGGCGGACCACCGCCGCCGAGCGTCCGGCTTCGCAGGGAGCTGCGCAGCTCTTCGTGCGCCGCCAACTCTGAC
TCCGCCGTCGACGTTGACCTCGATGCCCTCGTTGTCGGGGCCGGCTTCGCCGGCGTCTTCATGCTCAAGACGCTG
CGGGAGCGCGGCCTCCGCGTCCGCATCTACGAGGCCGGTACCGACCTCGGCGGCACCTGGCGCTGGAACTCATAT
CCTGGCGCGGCCGTCGACAGCGAGACGCCCGAGTACGAGTTCTCCTGGCCCGAGGTTTGGAAGAGCTGGAACTGG
ACGACCAACTATCCGCAGTTCAAGGAGCTCCGGGCCTACTTCGACCACGTCGACAAGGTGCTTCACATCAAGAAG
GACTGCTCCTTCAACACCGTCGTCACCGGCGCCGAGTTTGACATCCAAATGGGCCGCTGGAGGGTCCGGACTGAC
GACGGGAGACTCACGACGGCAAAGTATCTGATCTTGGGAACCGGCTTCTCCGCCAAGCGATATGTGCCGGAATGG
CCCGGGATCAACGACTTCAAGGGCATCATCCACCACTCATCCTTCTGGCCGGACGAGAACATCGCTGTCGGCGGC
AAGAAGTGCGCCGTCATCGGCACCGGCGCCTCCGGCGTGCAAATTGTCCAGGCCTGGGGCCCCGAGGCCAAGGAA
TTGAAAGTCTTCCAACGGACTCCCAACCTCGCCGTTCCCATGCGCCGGCGCCAGCTCACGGCCGAGGATCAGGAG
CCGGGCAAGAAGTGGTACGGCGAGCTGTTTAGGTTCCGCGAAAAGACCTTTGGCGGCTTCCTGTACGACTGGTAC
GAGAAGAACACCTTCGACGAGACGGCCGAGCAGCGGCAGGCTTGCTACGAGGAGGCCTGGAAGGCCGGTGGCTTC
CGCTTCTGGCTAAGCATCTACAAGGACAACCTGTTCAACGCCGAGGCCAACCGGGAGTCCTATCGATTCTGGGCC
GAAAAGACGCGCGAAAGGATCGACGACGACCGCAACAAGGACCTGCTCGCCCCCTTGGAGATGCCTCACTTCTTC
GGAATTAAAAGGCCGTGCCTCGAACACGACTACTACGAGCAGTTCAACCGTCCGTCGGTCCATGTCCTCGACATC
AAGGACGACCCGATCGAACGGTTTACTGAGACCGGAATCACCCTCAGGAGCGGAGCACACCATGACTTCGACGTC
GTGGCCGTTGCCACAGGTTTCGACGTTGTTACAGGAGCCATGACCCAGCTGGGCCTGAAGAGCATCGACAACCAG
ATGCTGGAAGAGCAGTGGGCGACTGGGGCGAACACCTACCTAGGGGTCAGCGTCAGCGGCTATCCCAACATGTTC
CACATGTACGGCGCCCACGGGCCGACGCTGCTGAGCAACGGGCCGCCCTGCATCGAAATTCAGGGCCGCTGGATC
GCCGACTGCATCGAAAAGATGGAGCTCAACAAAATCAAGGTCCTGAACCCAAAACCGGAGGCCTCGGTCGCGTGG
AAAAAGCAAATCAATCAGCTCTACAGCACCACCCTCTTCCCGACAACACAGTCGACCTACATGGGCGGCTCCATA
CCCGGCAAAGTCTCCGAGCCCATCTGCTTCGGCGGCGGACTGCCTGCGTACGCAACCGCGCTTCGGTCTGCTCTC
GAAAGCATGGACGGTTTCGAGATCGAGTACGAGTGA
Gene >Hirsu2|3631
ATGAACGGCGGGTCGGCATCGCAGAACGGCGGGGGACAGAACGGAGGGCCGGTGCCGCAGAACGGCGGGGGACAG
AACGGCGGACCACCGCCGCCGAGCGTCCGGCTTCGCAGGGAGCTGCGCAGCTCTTCGTGCGCCGCCAACTCTGAC
TCCGCCGTCGACGTTGACCTCGATGCCCTCGTTGTCGGGGCCGGCTTCGGTCCGTCCAACCCGATTTCCGAGTGA
GAGAGAAAAGGAAAGAGAGCAAGATGGGCGCGCAGGTCGCGATGCTGACCGCGCACAGCCGGCGTCTTCATGCTC
AAGACGCTGCGGGAGCGCGGCCTCCGCGTCCGCATCTACGAGGCCGGTACCGACCTCGGCGGCACCTGGCGCTGG
AACTCATATCCTGGCGCGGCCGTCGACAGCGAGACGCCCGAGTACGAGTTCTCCTGGCCCGAGGTTTGGAAGAGC
TGGAACTGGACGACCAACTATCCGCAGTTCAAGGAGCTCCGGGCCTACTTCGACCACGTCGACAAGGTGCTTCAC
ATCAAGAAGGACTGCTCCTTCAACACCGTCGTCACCGGCGCCGAGTTTGACATCCAAATGGGCCGCTGGAGGGTC
CGGACTGACGACGGGAGACTCACGACGGCAAAGTATCTGATCTTGGGAACCGGCTTCGTACGTCTCATCCTCTTC
TACATGTTATAACCCCCCCTTCCCCTCTTGTTCCGATGAAACCGTCGAATATCCCGACATCATTCAGGGAAAACC
GGAACCCCTTCTCGTCTTCATGACATCAAGGGATAACTGCCCTGTCCGCTCGCGCTCACGTCTCGAGTTGGCTCT
AGTCCGCCAAGCGATATGTGCCGGAATGGCCCGGGATCAACGACTTCAAGGGCATCATCCACCACTCATCCTTCT
GGCCGGACGAGAACATCGCTGTCGGCGGCAAGAAGTGCGCCGTCATCGGCACCGGCGCCTCCGGCGTGCAAATTG
TCCAGGCCTGGGGCCCCGAGGCCAAGGAATTGAAAGTCTTCCAACGGACTCCCAACCTCGCCGTTCCCATGCGCC
GGCGCCAGCTCACGGCCGAGGATCAGGAGCCGGGCAAGAAGTGGTACGGCGAGCTGTTTAGGTTCCGCGAAAAGA
CCTTTGGCGGCTTCCTGTACGACTGGTACGAGAAGAACACCTTCGACGAGACGGCCGAGCAGCGGCAGGCTTGCT
ACGAGGAGGCCTGGAAGGCCGGTGGCTTCCGCTTCTGGCTAAGCATCTACAAGGACAACCTGTTCAACGCCGAGG
CCAACCGGGAGTCCTATCGATTCTGGGCCGAAAAGACGCGCGAAAGGATCGACGACGACCGCAACAAGGACCTGC
TCGCCCCCTTGGAGATGCCTCACTTCTTCGGAATTAAAAGGCCGTGCCTCGAACACGACTACTACGAGCAGTTCA
ACCGTCCGTCGGTCCATGTCCTCGACATCAAGGACGACCCGATCGAACGGTTTACTGAGACCGGAATCACCCTCA
GGAGCGGAGCACACCATGACTTCGACGTCGTGGCCGTTGCCACAGGTTTCGTGAGTCCAATCCCCCCTTCCCCTC
CGACCGATGCAACCTCGTTTGCAGCAGTCCAGCCTCAGCAACCGAACCTGAAAAACTCACCATCTTGATGTTCCG
TCACGCTCCAGGACGTTGTTACAGGAGGTAAGCTTCGCATTCCTTCCGCCCCGAAGCCGCCGTCGAGAGCGCACC
GGGAACGGATATAGCTCTGGCTGACAGCTCTTCCTCGCCGCAGCCATGACCCAGCTGGGCCTGAAGAGCATCGAC
AACCAGATGCTGGAAGAGCAGTGGGCGACTGGGGCGAACACCTACCTAGGGGTCAGCGTCAGCGGCTATCCCAAC
ATGTTCCACATGTACGGCGCCCACGGGCCGACGCTGCTGAGCAACGGGCCGCCCTGCATCGAAATTCAGGGCCGC
TGGATCGCCGACTGCATCGAAAAGATGGAGCTCAACAAAATCAAGGTCCTGAACCCAAAACCGGAGGCCTCGGTC
GCGTGGAAAAAGCAAATCAATCAGCTCTACAGCACCACCCTCTTCCCGACAACACAGTCGACCTACATGGGCGGC
TCCATACCCGGCAAAGTCTCCGAGCCCATCTGCTTCGGCGGCGGACTGCCTGCGTACGCAACCGCGCTTCGGTCT
GCTCTCGAAAGCATGGACGGTTTCGAGATCGAGTACGAGTGA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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