Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauB2|2822
Gene name
LocationContig_193:20814..22838
Strand+
Gene length (bp)2024
Transcript length (bp)1785
Coding sequence length (bp)1785
Protein length (aa) 595

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00743 FMO-like Flavin-binding monooxygenase-like 1.4E-15 49 204
PF00743 FMO-like Flavin-binding monooxygenase-like 2.4E-05 360 522
PF13738 Pyr_redox_3 Pyridine nucleotide-disulphide oxidoreductase 2.8E-08 70 201
PF07992 Pyr_redox_2 Pyridine nucleotide-disulphide oxidoreductase 3.3E-11 3 200
PF13434 Lys_Orn_oxgnase L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase 9.3E-07 75 202

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 3 527 2.0E-23
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 3 516 9.0E-23
sp|Q5REK0|FMO2_PONAB Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 3 516 2.0E-20
sp|Q99518|FMO2_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 3 497 4.0E-20
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 3 516 8.0E-20
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Swissprot ID Swissprot Description Start End E-value
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 3 527 2.0E-23
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 3 516 9.0E-23
sp|Q5REK0|FMO2_PONAB Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 3 516 2.0E-20
sp|Q99518|FMO2_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 3 497 4.0E-20
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 3 516 8.0E-20
sp|P17635|FMO2_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 3 516 6.0E-19
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 3 527 5.0E-18
sp|P36366|FMO2_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 3 527 6.0E-18
sp|Q6IRI9|FMO2_RAT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 3 527 2.0E-17
sp|Q9EQ76|FMO3_RAT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 3 516 1.0E-14
sp|P31512|FMO4_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 3 202 8.0E-13
sp|P36365|FMO1_RAT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 3 187 4.0E-12
sp|Q95LA2|FMO1_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 3 184 1.0E-11
sp|P16549|FMO1_PIG Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 3 187 1.0E-11
sp|Q8MP06|SNO1_TYRJA Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 3 361 2.0E-11
sp|Q01740|FMO1_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 3 187 7.0E-11
sp|P36367|FMO4_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 3 202 8.0E-11
sp|P50285|FMO1_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 3 187 1.0E-10
sp|P97501|FMO3_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 3 209 1.0E-10
sp|Q9SVU0|YUC8_ARATH Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 6 210 4.0E-10
sp|Q8VHG0|FMO4_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 3 202 4.0E-10
sp|O60774|FMO6_HUMAN Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 3 184 4.0E-10
sp|Q8K4B7|FMO4_RAT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 3 202 5.0E-10
sp|Q8SPQ7|FMO3_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 3 209 6.0E-10
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 3 434 1.0E-09
sp|Q9LKC0|YUC5_ARATH Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 6 210 2.0E-09
sp|Q8VZ59|YUC6_ARATH Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 6 208 2.0E-09
sp|P17636|FMO1_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 3 184 3.0E-09
sp|O49312|YUC7_ARATH Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 6 210 4.0E-09
sp|O64489|YUC9_ARATH Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 6 210 6.0E-09
sp|Q9FVQ0|YUC10_ARATH Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 4 184 1.0E-08
sp|P31513|FMO3_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 3 516 6.0E-08
sp|Q7YS44|FMO3_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 3 516 7.0E-08
sp|Q9LPL3|YUC11_ARATH Probable indole-3-pyruvate monooxygenase YUCCA11 OS=Arabidopsis thaliana GN=YUC11 PE=2 SV=1 4 200 2.0E-07
sp|P49326|FMO5_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 3 518 7.0E-07
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 3 202 7.0E-07
sp|Q95LA1|FMO3_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 3 202 2.0E-06
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GO

GO Term Description Terminal node
GO:0050661 NADP binding Yes
GO:0016491 oxidoreductase activity Yes
GO:0050660 flavin adenine dinucleotide binding Yes
GO:0004499 N,N-dimethylaniline monooxygenase activity Yes
GO:1901265 nucleoside phosphate binding No
GO:0036094 small molecule binding No
GO:0043168 anion binding No
GO:0004497 monooxygenase activity No
GO:0005488 binding No
GO:0003674 molecular_function No
GO:1901363 heterocyclic compound binding No
GO:0003824 catalytic activity No
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen No
GO:0097159 organic cyclic compound binding No
GO:0043167 ion binding 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

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 35 0.45

Transmembrane Domains

Domain # Start End Length
1 541 563 22

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 >OphauB2|2822
MLKVAVIGGGPAGLATLKFLATAHHFFPIPPVEARLFEAECQIGGTFLVSSKYLTAFSDFRLPLDAPDFVTPQVY
VQYLMDYVARFELEPMIECQAKVTRVSRGEGGLGHLVQVSKPSGQCFDFVCDAVAICSGINVNPIIPKIEGINRV
ATVLHSSKLKKRQQFGQGTHVVVCGAGETGMDIAHLAVTSPTASVTLCHRDGFFCAPKIIPTPVHRSQKGAVRPN
KPVDASVASLFDTAYAHPVLQRSQLLWTAYDQWVKKMHLAVSGTEEGPDQWVGQISRERKYLDSIFLCKSDKALP
YISEGHRSQSLWNRMRSSLLNVPIKKTFGRRIHVRKWPTKIDKHGWMHFADSDVKCVRPNVIVFATGYKSQFDFL
DADYPLLGQADVRGIYKTDHVSVGYIGFVRPSIGAIPPLAELQAQLWVLRLLQASFPSQVPQTPGPNAVEAYQLD
YALHARQGYDFFANKRGVDHESYAYQLALDMGSAPTISYVATKGWKLFFTWAMGSNFNPKFRLVGPWRDEACAEH
VMRGELYGVVKRSGGFIYLVTYSIIPMIIFGLLSILLYAVTGIKAAFVSAVGTPASKVPRLFKSSKTRF*
Coding >OphauB2|2822
ATGCTCAAGGTTGCCGTCATTGGTGGCGGCCCAGCTGGGCTTGCAACGCTCAAGTTTCTCGCCACTGCCCACCAC
TTCTTCCCTATCCCCCCTGTTGAGGCTCGTCTCTTTGAGGCCGAGTGTCAAATCGGCGGCACTTTTCTCGTCTCA
TCCAAATATCTCACGGCCTTTTCTGATTTTCGTCTGCCGCTCGACGCCCCAGATTTTGTCACGCCGCAGGTATAT
GTGCAGTATCTGATGGACTATGTTGCCAGGTTTGAGCTCGAGCCCATGATTGAATGCCAGGCCAAGGTAACTCGC
GTCAGCCGCGGTGAGGGTGGCCTAGGCCATCTTGTCCAAGTCAGCAAGCCCTCAGGCCAGTGTTTTGATTTCGTC
TGCGACGCTGTAGCCATCTGCTCCGGCATCAACGTCAACCCTATAATCCCCAAGATCGAGGGCATCAACAGGGTG
GCCACTGTGCTTCACTCATCCAAGCTCAAGAAGCGTCAGCAGTTTGGCCAAGGCACTCATGTTGTTGTCTGTGGT
GCCGGCGAGACAGGCATGGACATTGCCCATCTGGCTGTCACGTCGCCCACTGCTTCTGTCACGCTCTGCCATCGA
GACGGCTTCTTTTGTGCTCCCAAGATCATCCCGACGCCGGTGCACCGGAGCCAAAAGGGGGCCGTCAGACCCAAC
AAGCCTGTCGACGCCTCGGTTGCAAGTCTCTTCGACACGGCGTATGCCCACCCTGTCCTGCAGCGAAGCCAGCTC
CTCTGGACGGCCTACGACCAATGGGTCAAGAAGATGCACCTTGCCGTGTCCGGGACTGAGGAGGGACCGGATCAG
TGGGTTGGCCAGATCAGCCGCGAGCGCAAGTATCTCGACTCGATATTCCTCTGCAAGTCGGACAAGGCTCTGCCC
TATATATCTGAAGGCCATCGCTCGCAGTCGCTCTGGAACCGCATGCGGTCGTCCTTGCTCAACGTGCCCATCAAG
AAGACTTTTGGTCGCCGCATCCATGTGCGCAAGTGGCCAACCAAGATCGACAAGCATGGCTGGATGCACTTTGCC
GACAGCGACGTCAAGTGCGTGCGCCCCAACGTCATTGTCTTTGCCACGGGCTACAAGAGCCAGTTTGACTTTCTC
GACGCCGACTACCCGCTGCTAGGCCAGGCCGATGTTCGGGGCATCTACAAGACGGACCATGTCTCCGTCGGCTAC
ATTGGCTTTGTGCGCCCGTCCATTGGCGCCATTCCACCGCTGGCTGAGCTCCAAGCCCAACTCTGGGTCTTGCGG
CTGCTCCAGGCCAGCTTTCCAAGCCAGGTGCCGCAGACGCCAGGGCCAAATGCCGTCGAGGCCTACCAGCTAGAC
TATGCTCTGCATGCGCGTCAGGGCTACGATTTCTTCGCCAACAAGCGAGGCGTTGATCACGAGTCGTATGCCTAC
CAGCTTGCCCTCGATATGGGATCAGCTCCCACCATCTCCTACGTTGCCACCAAGGGCTGGAAACTCTTCTTCACC
TGGGCCATGGGCTCCAACTTCAATCCCAAGTTCCGCCTCGTCGGGCCATGGAGGGACGAAGCCTGCGCCGAGCAC
GTTATGCGTGGCGAGCTGTATGGAGTCGTCAAGCGGTCGGGGGGCTTCATCTATCTCGTCACCTACTCCATTATC
CCAATGATCATTTTTGGTCTTTTGAGCATTCTGCTCTATGCCGTGACGGGAATCAAGGCGGCATTCGTCTCTGCT
GTTGGCACGCCAGCCTCCAAGGTCCCGCGACTTTTCAAGAGCTCCAAGACGCGCTTTTAA
Transcript >OphauB2|2822
ATGCTCAAGGTTGCCGTCATTGGTGGCGGCCCAGCTGGGCTTGCAACGCTCAAGTTTCTCGCCACTGCCCACCAC
TTCTTCCCTATCCCCCCTGTTGAGGCTCGTCTCTTTGAGGCCGAGTGTCAAATCGGCGGCACTTTTCTCGTCTCA
TCCAAATATCTCACGGCCTTTTCTGATTTTCGTCTGCCGCTCGACGCCCCAGATTTTGTCACGCCGCAGGTATAT
GTGCAGTATCTGATGGACTATGTTGCCAGGTTTGAGCTCGAGCCCATGATTGAATGCCAGGCCAAGGTAACTCGC
GTCAGCCGCGGTGAGGGTGGCCTAGGCCATCTTGTCCAAGTCAGCAAGCCCTCAGGCCAGTGTTTTGATTTCGTC
TGCGACGCTGTAGCCATCTGCTCCGGCATCAACGTCAACCCTATAATCCCCAAGATCGAGGGCATCAACAGGGTG
GCCACTGTGCTTCACTCATCCAAGCTCAAGAAGCGTCAGCAGTTTGGCCAAGGCACTCATGTTGTTGTCTGTGGT
GCCGGCGAGACAGGCATGGACATTGCCCATCTGGCTGTCACGTCGCCCACTGCTTCTGTCACGCTCTGCCATCGA
GACGGCTTCTTTTGTGCTCCCAAGATCATCCCGACGCCGGTGCACCGGAGCCAAAAGGGGGCCGTCAGACCCAAC
AAGCCTGTCGACGCCTCGGTTGCAAGTCTCTTCGACACGGCGTATGCCCACCCTGTCCTGCAGCGAAGCCAGCTC
CTCTGGACGGCCTACGACCAATGGGTCAAGAAGATGCACCTTGCCGTGTCCGGGACTGAGGAGGGACCGGATCAG
TGGGTTGGCCAGATCAGCCGCGAGCGCAAGTATCTCGACTCGATATTCCTCTGCAAGTCGGACAAGGCTCTGCCC
TATATATCTGAAGGCCATCGCTCGCAGTCGCTCTGGAACCGCATGCGGTCGTCCTTGCTCAACGTGCCCATCAAG
AAGACTTTTGGTCGCCGCATCCATGTGCGCAAGTGGCCAACCAAGATCGACAAGCATGGCTGGATGCACTTTGCC
GACAGCGACGTCAAGTGCGTGCGCCCCAACGTCATTGTCTTTGCCACGGGCTACAAGAGCCAGTTTGACTTTCTC
GACGCCGACTACCCGCTGCTAGGCCAGGCCGATGTTCGGGGCATCTACAAGACGGACCATGTCTCCGTCGGCTAC
ATTGGCTTTGTGCGCCCGTCCATTGGCGCCATTCCACCGCTGGCTGAGCTCCAAGCCCAACTCTGGGTCTTGCGG
CTGCTCCAGGCCAGCTTTCCAAGCCAGGTGCCGCAGACGCCAGGGCCAAATGCCGTCGAGGCCTACCAGCTAGAC
TATGCTCTGCATGCGCGTCAGGGCTACGATTTCTTCGCCAACAAGCGAGGCGTTGATCACGAGTCGTATGCCTAC
CAGCTTGCCCTCGATATGGGATCAGCTCCCACCATCTCCTACGTTGCCACCAAGGGCTGGAAACTCTTCTTCACC
TGGGCCATGGGCTCCAACTTCAATCCCAAGTTCCGCCTCGTCGGGCCATGGAGGGACGAAGCCTGCGCCGAGCAC
GTTATGCGTGGCGAGCTGTATGGAGTCGTCAAGCGGTCGGGGGGCTTCATCTATCTCGTCACCTACTCCATTATC
CCAATGATCATTTTTGGTCTTTTGAGCATTCTGCTCTATGCCGTGACGGGAATCAAGGCGGCATTCGTCTCTGCT
GTTGGCACGCCAGCCTCCAAGGTCCCGCGACTTTTCAAGAGCTCCAAGACGCGCTTTTAA
Gene >OphauB2|2822
ATGCTCAAGGTTGCCGTCATTGGTGGCGGCCCAGCTGGGCTTGCAACGCTCAAGTTTCTCGCCACTGCCCACCAC
TTCTTCCCTATCCCCCCTGTTGAGGCTCGTCTCTTTGAGGCCGAGTGTCAAATCGGCGGCACTTTTGTCCATCGT
ATATATGAAGACGCCGAGGCGAGTCCTCCCCCGGTGTTGGCTGGTGGCTCCACGTCATGCTTATGCAAAGCAGCT
CGTCTCATCCAAATATCTCACGGCCTTTTCTGATTTTCGTCTGCCGCTCGACGCCCCAGATTTTGTCACGCCGCA
GGTATATGTGCAGTATCTGATGGACTATGTTGCCAGGTTTGAGCTCGAGCCCATGATTGAATGCCAGGCCAAGGT
AACTCGCGTCAGCCGCGGTGAGGGTGGCCTAGGCCATCTTGTCCAAGTCAGCAAGCCCTCAGGCCAGTGTTTTGA
TTTCGTCTGCGACGCTGTAGCCATCTGCTCCGGCATCAACGTCAACCCTATAATCCCCAAGATCGAGGGCATCAA
CAGGGTGGCCACTGTGCTTCACTCATCCAAGCTCAAGAAGCGTCAGCAGTTTGGCCAAGGCACTCATGTTGTTGT
CTGTGGTGCCGGCGAGACAGGCATGGACATTGCCCATCTGGCTGTCACGTCGCCCACTGCTTCTGTCACGCTCTG
CCATCGAGACGGCTTCTTTTGTGCTCCCAAGGCAAGTCGCCCAAAAGAAAAGCTCAAGCCCAACGCCTTGTTCCG
TGTGCTCATGGTCAATGCTAGATCATCCCGACGCCGGTGCACCGGAGCCAAAAGGGGGCCGTCAGACCCAACAAG
CCTGTCGACGCCTCGGTTGCAAGTCTCTTCGACACGGCGTATGCCCACCCTGTCCTGCAGCGAAGCCAGCTCCTC
TGGACGGCCTACGACCAATGGGTCAAGAAGATGCACCTTGCCGTGTCCGGGACTGAGGAGGGACCGGATCAGTGG
GTTGGCCAGATCAGCCGCGAGCGCAAGTATCTCGACTCGATATTCCTCTGCAAGTCGGACAAGGCTCTGCCCTAT
ATATCTGAAGGCCATCGCTCGCAGTCGCTCTGGAACCGCATGCGGTCGTCCTTGCTCAACGTGCCCATCAAGAAG
ACTTTTGGTCGCCGCATCCATGTGCGCAAGTGGCCAACCAAGATCGACAAGCATGGCTGGATGCACTTTGCCGAC
AGCGACGTCAAGTGCGTGCGCCCCAACGTCATTGTCTTTGCCACGGGCTACAAGAGCCAGTTTGACTTTCTCGAC
GCCGACTACCCGCTGCTAGGCCAGGCCGATGTTCGGGGCATCTACAAGACGGACCATGTCTCCGTCGGCTACATT
GGCTTTGTGCGCCCGTCCATTGGCGCCATTCCACCGCTGGCTGAGCTCCAAGCCCAACTCTGGGTCTTGCGGCTG
CTCCAGGCCAGCTTTCCAAGCCAGGTGCCGCAGACGCCAGGGCCAAATGCCGTCGAGGCCTACCAGCTAGACTAT
GCTCTGCATGCGCGTCAGGGCTACGATTTCTTCGCCAACAAGCGAGGCGTTGATCACGAGTCGTATGCCTACCAG
CTTGCCCTCGATATGGGATCAGCTCCCACCATCTCCTACGTTGCCACCAAGGGCTGGAAACTCTTCTTCACCTGG
GCCATGGGCTCCAACTTCAATCCCAAGTTCCGCCTCGTCGGGCCATGGAGGGACGAAGCCTGCGCCGAGCACGTT
ATGCGTGGCGAGCTGTATGGAGTCGTCAAGCGGTCGGGGGGCTTCATCTGTGAGTTGTTTCCCTCTTGAATTTCC
CTCTTGAATTTCCCTCTTGAATTTCCCTCTTGGAGCCGTGCCAAGGACTGGCTGACGGCTTTGCAGATCTCGTCA
CCTACTCCATTATCCCAATGATCATTTTTGGTCTTTTGAGCATTCTGCTCTATGCCGTGACGGGAATCAAGGCGG
CATTCGTCTCTGCTGTTGGCACGCCAGCCTCCAAGGTCCCGCGACTTTTCAAGAGCTCCAAGACGCGCTTTTAA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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