Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|3636
Gene name
LocationContig_197:15777..17581
Strand+
Gene length (bp)1804
Transcript length (bp)1488
Coding sequence length (bp)1488
Protein length (aa) 496

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00743 FMO-like Flavin-binding monooxygenase-like 6.2E-12 74 230
PF13450 NAD_binding_8 NAD(P)-binding Rossmann-like domain 6.9E-06 15 83

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|Q9RKB5|BVMO2_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 1 479 7.0E-74
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 1 473 2.0E-60
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 13 463 2.0E-57
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 13 463 2.0E-57
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 13 463 2.0E-57
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|Q9RKB5|BVMO2_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 1 479 7.0E-74
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 1 473 2.0E-60
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 13 463 2.0E-57
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 13 463 2.0E-57
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 13 463 2.0E-57
sp|P55487|Y4ID_RHISN Uncharacterized monooxygenase y4iD OS=Rhizobium sp. (strain NGR234) GN=NGR_a03290 PE=3 SV=1 7 461 3.0E-50
sp|Q93TJ5|HAPMO_PSEFL 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 12 480 1.0E-46
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 12 492 5.0E-40
sp|Q47PU3|PAMO_THEFY Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 1 472 5.0E-38
sp|P12015|CHMO_ACISP Cyclohexanone 1,2-monooxygenase OS=Acinetobacter sp. PE=1 SV=2 21 448 2.0E-36
sp|H3JQW0|OTEMO_PSEPU 2-oxo-Delta(3)-4,5,5-trimethylcyclopentenylacetyl-CoA monooxygenase OS=Pseudomonas putida GN=otemo PE=1 SV=1 15 472 4.0E-35
sp|A7HU16|BVMO_PARL1 Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 38 473 7.0E-35
sp|P9WNF8|ETHA_MYCTO FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ethA PE=3 SV=1 13 389 5.0E-29
sp|Q7TVI2|ETHA_MYCBO FAD-containing monooxygenase EthA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ethA PE=1 SV=1 13 389 5.0E-29
sp|P9WNF9|ETHA_MYCTU FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ethA PE=1 SV=1 13 389 5.0E-29
sp|E3VWK3|PENE_STREX Pentalenolactone D synthase OS=Streptomyces exfoliatus GN=penE PE=1 SV=1 13 454 8.0E-28
sp|E3VWI7|PNTE_STRAE Pentalenolactone D synthase OS=Streptomyces arenae GN=pntE PE=1 SV=1 13 387 2.0E-26
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 3 390 5.0E-26
sp|Q88J44|BVMO_PSEPK Baeyer-Villiger monooxygenase OS=Pseudomonas putida (strain KT2440) GN=PP_2805 PE=1 SV=1 13 389 1.0E-25
sp|P9WNF7|MYMA_MYCTU Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mymA PE=1 SV=1 13 389 1.0E-25
sp|P9WNF6|MYMA_MYCTO Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=mymA PE=3 SV=1 13 389 1.0E-25
sp|A0R665|ETHA_MYCS2 FAD-containing monooxygenase EthA OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=ethA PE=3 SV=1 13 432 2.0E-24
sp|Q9RL17|BVMO1_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO0300 PE=1 SV=1 31 479 8.0E-23
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 38 454 1.0E-21
sp|A3U3H1|BVMO_OCEBH Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 15 215 3.0E-21
sp|U5S003|BVMO4_DIESD Baeyer-Villiger monooxygenase 4 OS=Dietzia sp. (strain D5) PE=1 SV=1 34 210 3.0E-17
sp|Q8VZ59|YUC6_ARATH Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 16 344 1.0E-15
sp|Q9LMA1|FMO1_ARATH Probable flavin-containing monooxygenase 1 OS=Arabidopsis thaliana GN=FMO1 PE=2 SV=1 11 350 1.0E-15
sp|Q8GAW0|CPMO_COMS9 Cyclopentanone 1,2-monooxygenase OS=Comamonas sp. (strain NCIMB 9872) GN=cpnB PE=1 SV=3 47 473 1.0E-15
sp|Q9FVQ0|YUC10_ARATH Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 13 353 1.0E-13
sp|Q8K4B7|FMO4_RAT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 12 226 5.0E-12
sp|O23024|YUC3_ARATH Probable indole-3-pyruvate monooxygenase YUCCA3 OS=Arabidopsis thaliana GN=YUC3 PE=2 SV=1 16 210 1.0E-11
sp|Q8MP06|SNO1_TYRJA Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 6 206 2.0E-11
sp|O49312|YUC7_ARATH Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 16 232 2.0E-11
sp|A3U3H1|BVMO_OCEBH Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 290 391 3.0E-11
sp|Q8VHG0|FMO4_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 12 232 3.0E-11
sp|Q9LFM5|YUC4_ARATH Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 16 344 6.0E-11
sp|U5S003|BVMO4_DIESD Baeyer-Villiger monooxygenase 4 OS=Dietzia sp. (strain D5) PE=1 SV=1 280 480 3.0E-10
sp|Q9LKC0|YUC5_ARATH Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 16 232 3.0E-10
sp|Q9SXE1|GSOX3_ARATH Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 1 206 3.0E-10
sp|P17636|FMO1_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 12 209 4.0E-10
sp|Q9SVQ1|YUC2_ARATH Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 16 344 6.0E-10
sp|O64489|YUC9_ARATH Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 16 232 7.0E-10
sp|P36367|FMO4_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 12 209 9.0E-10
sp|P31512|FMO4_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 12 209 1.0E-09
sp|P17635|FMO2_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 12 275 2.0E-09
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 12 231 2.0E-09
sp|Q9FWW6|GSXL1_ARATH Flavin-containing monooxygenase FMO GS-OX-like 1 OS=Arabidopsis thaliana GN=At1g12160 PE=2 SV=1 13 198 3.0E-09
sp|Q9SVU0|YUC8_ARATH Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 16 239 6.0E-09
sp|P97501|FMO3_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 12 209 8.0E-09
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 12 231 1.0E-08
sp|Q9FWW3|GSXL6_ARATH Flavin-containing monooxygenase FMO GS-OX-like 6 OS=Arabidopsis thaliana GN=At1g12130 PE=2 SV=1 38 198 1.0E-08
sp|A8MRX0|GSOX5_ARATH Flavin-containing monooxygenase FMO GS-OX5 OS=Arabidopsis thaliana GN=FMOGS-OX5 PE=2 SV=2 38 204 2.0E-08
sp|Q9EQ76|FMO3_RAT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 12 209 2.0E-08
sp|Q5REK0|FMO2_PONAB Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 12 213 2.0E-08
sp|Q9SS04|GSOX1_ARATH Flavin-containing monooxygenase FMO GS-OX1 OS=Arabidopsis thaliana GN=FMOGS-OX1 PE=2 SV=1 1 198 2.0E-08
sp|Q01740|FMO1_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 12 202 3.0E-08
sp|Q6IRI9|FMO2_RAT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 12 209 3.0E-08
sp|Q95LA2|FMO1_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 12 209 4.0E-08
sp|P36366|FMO2_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 12 209 5.0E-08
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 12 213 5.0E-08
sp|Q9FKE7|FMO2_ARATH Putative flavin-containing monooxygenase 2 OS=Arabidopsis thaliana GN=FMO2 PE=3 SV=2 11 350 5.0E-08
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 12 231 5.0E-08
sp|P16549|FMO1_PIG Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 12 209 6.0E-08
sp|Q9FWW9|GSXL2_ARATH Flavin-containing monooxygenase FMO GS-OX-like 2 OS=Arabidopsis thaliana GN=At1g12200 PE=2 SV=1 63 204 6.0E-08
sp|Q9LPL3|YUC11_ARATH Probable indole-3-pyruvate monooxygenase YUCCA11 OS=Arabidopsis thaliana GN=YUC11 PE=2 SV=1 13 344 7.0E-08
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 12 213 8.0E-08
sp|Q99518|FMO2_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 12 213 9.0E-08
sp|Q94K43|GSOX2_ARATH Flavin-containing monooxygenase FMO GS-OX2 OS=Arabidopsis thaliana GN=FMOGS-OX2 PE=2 SV=1 56 198 1.0E-07
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 12 209 1.0E-07
sp|Q9FF12|GSXL9_ARATH Flavin-containing monooxygenase FMO GS-OX-like 9 OS=Arabidopsis thaliana GN=At5g07800 PE=2 SV=1 70 198 2.0E-07
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 12 262 3.0E-07
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 12 209 5.0E-07
sp|Q8SPQ7|FMO3_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 12 209 5.0E-07
sp|P32417|FMO3_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 12 209 7.0E-07
sp|Q8HYJ9|FMO3_BOVIN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 12 228 9.0E-07
sp|Q93Y23|GSOX4_ARATH Flavin-containing monooxygenase FMO GS-OX4 OS=Arabidopsis thaliana GN=FMOGS-OX4 PE=2 SV=1 60 198 9.0E-07
sp|P36365|FMO1_RAT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 12 209 2.0E-06
sp|P50285|FMO1_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 12 209 3.0E-06
sp|P31513|FMO3_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 12 209 5.0E-06
sp|Q7YS44|FMO3_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 12 209 6.0E-06
sp|Q95LA1|FMO3_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 12 231 8.0E-06
sp|Q9SXD9|GSXL7_ARATH Flavin-containing monooxygenase FMO GS-OX-like 7 OS=Arabidopsis thaliana GN=At1g62580 PE=3 SV=2 7 173 8.0E-06
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GO

GO Term Description Terminal node
GO:0004499 N,N-dimethylaniline monooxygenase activity Yes
GO:0050661 NADP binding Yes
GO:0050660 flavin adenine dinucleotide binding Yes
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:0003674 molecular_function 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:0036094 small molecule binding 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
GO:0016491 oxidoreductase activity No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 27 0.45

Transmembrane Domains

(None)

Transcription Factor Class

(None)

Expression data

No expression data available for this genome

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 >Hirsu2|3636
MEKSQQPSSFSKVACIGSGISAIAVGATLKRWYGITDVCFFERHNHLGGTWFINQYPGIYSFHPNSTGPKTLASQ
RQLWGYLNDVAEEYDLTSKIRFKSTVKRCEWVESIRRWRIHVLNGVTGDVFVHECQFLFSGTGQLTEPRKPDKPG
IETFKGTVIYACRWKQDADLRNKNVVVVGNGCTATQIVPAISPQAKHLTQFVRSKHWVLPPLTIPFLPLFTFLSR
WIPGFLVLFRFLVFLLTENNVRGLYDTESAALYRERRRKQAESYMRKTAPEEYHDILIPDFEFGCKRRIFDSGYL
DALNYTNVSLTNNPIVEFVPEGVRTEQGITKADVIVLANGYSTNNYLPGVEVIGRGGQTAEEHWQKMGGPGAYNT
TLLSGFPNFFMVLGPNTLSGHTSAFMAVENSVNYSLRVMEPVLKGVADAVDVKHDAELDYVDDMQKASKRTVFMS
GGCSTWYTQTKDGEKPRNAMVYPYSQAWFWYQCLFPHYKDLDYLN*
Coding >Hirsu2|3636
ATGGAGAAGTCGCAACAGCCCTCCAGCTTCAGCAAGGTGGCCTGCATCGGCTCGGGCATCTCTGCCATTGCTGTG
GGAGCCACACTGAAGCGCTGGTATGGCATCACCGACGTGTGCTTCTTCGAGAGGCACAACCACCTCGGAGGGACG
TGGTTCATCAACCAGTACCCTGGTATCTATTCCTTCCACCCGAACTCGACCGGCCCCAAGACGCTGGCCTCGCAG
CGTCAGCTCTGGGGGTACCTCAACGACGTTGCGGAAGAGTATGACCTCACGTCCAAGATACGGTTCAAGTCGACT
GTCAAGCGCTGCGAGTGGGTGGAGAGCATCCGCCGCTGGCGCATCCACGTGCTGAACGGCGTCACGGGAGACGTG
TTCGTTCACGAATGCCAGTTTCTTTTCAGCGGCACCGGCCAGCTGACGGAGCCCCGAAAGCCGGACAAGCCTGGT
ATCGAGACTTTCAAGGGTACCGTCATCTACGCCTGCAGATGGAAGCAGGACGCCGACCTCCGGAACAAGAACGTC
GTCGTCGTCGGCAACGGCTGCACGGCTACCCAGATCGTGCCGGCCATCTCGCCGCAGGCCAAGCATCTAACGCAG
TTTGTGCGGTCGAAGCATTGGGTGCTGCCGCCGCTGACAATTCCCTTTCTTCCCCTGTTCACCTTCCTGTCCCGA
TGGATTCCCGGCTTCTTAGTCCTGTTCCGGTTCCTCGTCTTCCTCCTTACGGAGAACAACGTGCGCGGCCTGTAC
GACACTGAGTCGGCAGCGCTCTACAGAGAGAGACGCCGTAAGCAGGCTGAGAGTTACATGCGGAAGACAGCGCCG
GAGGAGTATCACGATATACTTATCCCGGATTTCGAGTTCGGGTGCAAGCGCCGCATCTTTGACTCGGGATATCTG
GACGCATTGAACTACACCAACGTCAGCCTGACCAACAACCCGATCGTCGAATTTGTCCCCGAGGGTGTACGCACA
GAGCAGGGCATCACCAAGGCCGACGTCATCGTTCTGGCGAACGGCTACTCGACAAATAACTACCTTCCGGGCGTC
GAAGTTATCGGCCGAGGAGGCCAGACGGCTGAGGAGCACTGGCAGAAGATGGGCGGGCCTGGCGCGTATAACACG
ACTCTGCTTAGCGGATTTCCTAACTTCTTTATGGTTCTCGGCCCTAACACACTAAGTGGCCATACGTCGGCCTTC
ATGGCGGTGGAGAACTCGGTTAACTACTCGCTACGAGTTATGGAGCCAGTTCTCAAGGGTGTCGCGGACGCTGTC
GATGTCAAGCACGACGCGGAGTTGGACTACGTGGACGATATGCAGAAGGCATCGAAGCGTACTGTCTTTATGTCT
GGCGGATGCTCCACCTGGTACACGCAGACCAAGGATGGTGAGAAGCCGCGTAACGCCATGGTCTATCCGTACTCG
CAGGCTTGGTTTTGGTATCAGTGCTTGTTCCCGCACTACAAGGACCTGGATTATCTGAACTAG
Transcript >Hirsu2|3636
ATGGAGAAGTCGCAACAGCCCTCCAGCTTCAGCAAGGTGGCCTGCATCGGCTCGGGCATCTCTGCCATTGCTGTG
GGAGCCACACTGAAGCGCTGGTATGGCATCACCGACGTGTGCTTCTTCGAGAGGCACAACCACCTCGGAGGGACG
TGGTTCATCAACCAGTACCCTGGTATCTATTCCTTCCACCCGAACTCGACCGGCCCCAAGACGCTGGCCTCGCAG
CGTCAGCTCTGGGGGTACCTCAACGACGTTGCGGAAGAGTATGACCTCACGTCCAAGATACGGTTCAAGTCGACT
GTCAAGCGCTGCGAGTGGGTGGAGAGCATCCGCCGCTGGCGCATCCACGTGCTGAACGGCGTCACGGGAGACGTG
TTCGTTCACGAATGCCAGTTTCTTTTCAGCGGCACCGGCCAGCTGACGGAGCCCCGAAAGCCGGACAAGCCTGGT
ATCGAGACTTTCAAGGGTACCGTCATCTACGCCTGCAGATGGAAGCAGGACGCCGACCTCCGGAACAAGAACGTC
GTCGTCGTCGGCAACGGCTGCACGGCTACCCAGATCGTGCCGGCCATCTCGCCGCAGGCCAAGCATCTAACGCAG
TTTGTGCGGTCGAAGCATTGGGTGCTGCCGCCGCTGACAATTCCCTTTCTTCCCCTGTTCACCTTCCTGTCCCGA
TGGATTCCCGGCTTCTTAGTCCTGTTCCGGTTCCTCGTCTTCCTCCTTACGGAGAACAACGTGCGCGGCCTGTAC
GACACTGAGTCGGCAGCGCTCTACAGAGAGAGACGCCGTAAGCAGGCTGAGAGTTACATGCGGAAGACAGCGCCG
GAGGAGTATCACGATATACTTATCCCGGATTTCGAGTTCGGGTGCAAGCGCCGCATCTTTGACTCGGGATATCTG
GACGCATTGAACTACACCAACGTCAGCCTGACCAACAACCCGATCGTCGAATTTGTCCCCGAGGGTGTACGCACA
GAGCAGGGCATCACCAAGGCCGACGTCATCGTTCTGGCGAACGGCTACTCGACAAATAACTACCTTCCGGGCGTC
GAAGTTATCGGCCGAGGAGGCCAGACGGCTGAGGAGCACTGGCAGAAGATGGGCGGGCCTGGCGCGTATAACACG
ACTCTGCTTAGCGGATTTCCTAACTTCTTTATGGTTCTCGGCCCTAACACACTAAGTGGCCATACGTCGGCCTTC
ATGGCGGTGGAGAACTCGGTTAACTACTCGCTACGAGTTATGGAGCCAGTTCTCAAGGGTGTCGCGGACGCTGTC
GATGTCAAGCACGACGCGGAGTTGGACTACGTGGACGATATGCAGAAGGCATCGAAGCGTACTGTCTTTATGTCT
GGCGGATGCTCCACCTGGTACACGCAGACCAAGGATGGTGAGAAGCCGCGTAACGCCATGGTCTATCCGTACTCG
CAGGCTTGGTTTTGGTATCAGTGCTTGTTCCCGCACTACAAGGACCTGGATTATCTGAACTAG
Gene >Hirsu2|3636
ATGGAGAAGTCGCAACAGCCCTCCAGCTTCAGCAAGGTGGCCTGCATCGGCTCGGGCATCTCTGCCATTGCTGTG
GGAGCCACACTGAAGCGCTGGTATGGCATCACCGACGTGTGCTTCTTCGAGAGGCACAACCACCTCGGAGGGACG
TGGTTCATCAACCAGTACCCTGGTATGTGACCCTAGACTCGAACGAGCATATAGTCGGGCCAGAATTGTATGTGT
TGATCGTTTGGTAATGTAGGTTGTGCTTGTGACGTGCCCAGCGTCTTGTACAGCTATTCCTTCCACCCGAACTCG
ACCGGCCCCAAGACGCTGGCCTCGCAGCGTCAGCTCTGGGGGTACCTCAACGACGTTGCGGAAGAGTATGACCTC
ACGTCCAAGATACGGTTCAAGTCGACTGTCAAGCGCTGCGAGTGGGTGGAGAGCATCCGCCGCTGGCGCATCCAC
GTGCTGAACGGCGTCACGGGAGACGTGTTCGTTCACGAATGCCAGTTTCTTTTCAGCGGCACCGGCCAGCTGACG
GAGCCCCGAAAGCCGGACAAGCCTGGTATCGAGACTTTCAAGGGTACCGTCATCTACGCCTGCAGATGGAAGCAG
GACGCCGACCTCCGGAACAAGAACGTCGTCGTCGTCGGCAACGGCTGCACGGCTACCCAGATCGTGCCGGCCATC
TCGCCGCAGGCCAAGCATCTAACGCAGTTTGTGCGGTCGAAGCATTGGGTGCTGCCGCCGCTGACAATTCCCTTT
CTTCCCCTGTTCACCTTCCTGTCCCGATGGATTCCCGGCTTCTTAGTCCTGTTCCGGTTCCTCGTCTTCCTCCTT
ACGGAGAACAACGTGCGCGGCCTGTACGACACTGAGTCGGCAGCGCTCTACAGAGAGAGACGCCGTAAGCAGGCT
GAGAGTTACATGCGGAAGACAGCGCCGGAGGAGTATCACGATATACTTATCCCGGATTTCGAGTTCGGGTGCAAG
CGCCGCATCTTTGACTCGGGATATCTGGACGCATTGAACTACACCAACGTCAGCCTGACCAACAACCCGATCGTC
GAATTTGTCCCCGAGGGTGTACGCACAGAGCAGGGCATCACCAAGGCCGACGTCATCGTTCTGGCGAACGGCTAC
TCGACAAATAACTACCTTCCGGGCGTCGAAGTTATCGGCCGAGGAGGCCAGACGGCTGAGGAGCACTGGCAGAAG
ATGGGCGGGCCTGGCGCGTATAACACGACTCTGCTTAGCGGATTTCCTAACTTCTTTATGGTTCTCGGTATGAGG
TCCCCGCCGCCGGGAAACAGTAGCTCGATACTGACGGACACTACTGCAGGCCCTAACACACTAAGTGGCCATACG
TCGGCCTTCATGGCGGTGGAGAACTCGGTTAACTACTCGCTACGAGTTATGGAGCCAGTTCTCAAGGGTGTCGCG
GACGCTGTCGATGTCAAGCACGACGCGGAGTTGGACTACGTGGACGATATGCAGAAGGCATCGAAGCGTACTGTC
TTTATGTCTGGCGGATGCTCCACCTGGTACACGCAGACCAAGGATGGTGAGAAGCCGCGTAACGCCATGGTCTAT
CCGTACTCGCAGGCTTGGTTTTGGTATCAGTGCTTGTTCCCGCACTACAAGGACCTGGATTATCTGGTACGTCTT
GGCTCTCACCGTGCCGTTGTCCAGAACAGGATATGTACTAACCCAAGTCCAACAGGGTCAAAAACAATCTATCTC
GGGCTCAAGGATAAGGATGCTTCTAGGAGCGGTCATTCTCGGAGTCTGGCCCCTGTTTACGCATATGCTCTAGAA
CTAG

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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