Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|3575
Gene name
LocationContig_195:1955..5229
Strand-
Gene length (bp)3274
Transcript length (bp)3054
Coding sequence length (bp)3054
Protein length (aa) 1018

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF12812 PDZ_1 PDZ-like domain 8.4E-36 395 471
PF12812 PDZ_1 PDZ-like domain 1.7E-17 870 947
PF13365 Trypsin_2 Trypsin-like peptidase domain 4.2E-18 107 252

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|A5DVI0|NM111_LODEL Pro-apoptotic serine protease NMA111 OS=Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) GN=NMA111 PE=3 SV=1 74 982 0.0E+00
sp|A4RJH4|NM111_MAGO7 Pro-apoptotic serine protease NMA111 OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=NMA111 PE=3 SV=1 1 1014 0.0E+00
sp|Q6CIT6|NM111_KLULA Pro-apoptotic serine protease NMA111 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=NMA111 PE=3 SV=1 73 981 0.0E+00
sp|A7TGI3|NM111_VANPO Pro-apoptotic serine protease NMA111 OS=Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294) GN=NMA111 PE=3 SV=1 74 988 0.0E+00
sp|A6ZRW1|NM111_YEAS7 Pro-apoptotic serine protease NMA111 OS=Saccharomyces cerevisiae (strain YJM789) GN=NMA111 PE=3 SV=1 75 982 0.0E+00
[Show all]
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Swissprot ID Swissprot Description Start End E-value
sp|A5DVI0|NM111_LODEL Pro-apoptotic serine protease NMA111 OS=Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) GN=NMA111 PE=3 SV=1 74 982 0.0E+00
sp|A4RJH4|NM111_MAGO7 Pro-apoptotic serine protease NMA111 OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=NMA111 PE=3 SV=1 1 1014 0.0E+00
sp|Q6CIT6|NM111_KLULA Pro-apoptotic serine protease NMA111 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=NMA111 PE=3 SV=1 73 981 0.0E+00
sp|A7TGI3|NM111_VANPO Pro-apoptotic serine protease NMA111 OS=Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294) GN=NMA111 PE=3 SV=1 74 988 0.0E+00
sp|A6ZRW1|NM111_YEAS7 Pro-apoptotic serine protease NMA111 OS=Saccharomyces cerevisiae (strain YJM789) GN=NMA111 PE=3 SV=1 75 982 0.0E+00
sp|P53920|NM111_YEAST Pro-apoptotic serine protease NMA111 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NMA111 PE=1 SV=1 75 982 0.0E+00
sp|Q75D90|NM111_ASHGO Pro-apoptotic serine protease NMA111 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=NMA111 PE=3 SV=2 65 988 0.0E+00
sp|A3LX99|NM111_PICST Pro-apoptotic serine protease NMA111 OS=Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) GN=NMA111 PE=3 SV=1 25 984 0.0E+00
sp|Q6FLE2|NM111_CANGA Pro-apoptotic serine protease NMA111 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=NMA111 PE=3 SV=1 50 995 0.0E+00
sp|Q9P7S1|YIFC_SCHPO PDZ domain-containing protein C23G3.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC23G3.12c PE=2 SV=1 74 994 0.0E+00
sp|A5DAL3|NM111_PICGU Pro-apoptotic serine protease NMA111 OS=Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN=NMA111 PE=3 SV=2 75 984 0.0E+00
sp|Q6BKM0|NM111_DEBHA Pro-apoptotic serine protease NMA111 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=NMA111 PE=3 SV=2 50 994 0.0E+00
sp|A1DP85|NM111_NEOFI Pro-apoptotic serine protease nma111 OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=nma111 PE=3 SV=2 74 1006 0.0E+00
sp|Q2H334|NM111_CHAGB Pro-apoptotic serine protease NMA111 OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=NMA111 PE=3 SV=1 1 1007 0.0E+00
sp|Q7S9D2|NM111_NEUCR Pro-apoptotic serine protease nma111 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=nma111 PE=3 SV=1 1 1007 0.0E+00
sp|Q6BZQ9|NM111_YARLI Pro-apoptotic serine protease NMA111 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=NMA111 PE=3 SV=2 70 988 0.0E+00
sp|Q0CSC0|NM111_ASPTN Pro-apoptotic serine protease nma111 OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=nma111 PE=3 SV=2 1 1006 0.0E+00
sp|Q4WLG1|NM111_ASPFU Pro-apoptotic serine protease nma111 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=nma111 PE=3 SV=1 74 1006 0.0E+00
sp|A1CUK5|NM111_ASPCL Pro-apoptotic serine protease nma111 OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=nma111 PE=3 SV=1 1 1005 0.0E+00
sp|Q2TYB1|NM111_ASPOR Pro-apoptotic serine protease nma111 OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=nma111 PE=3 SV=1 74 1006 0.0E+00
sp|A5AB13|NM111_ASPNC Pro-apoptotic serine protease nma111 OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=nma111 PE=3 SV=2 74 1006 0.0E+00
sp|Q1E3N5|NM111_COCIM Pro-apoptotic serine protease NMA111 OS=Coccidioides immitis (strain RS) GN=NMA111 PE=3 SV=2 73 994 0.0E+00
sp|Q0UY70|NM111_PHANO Pro-apoptotic serine protease NMA111 OS=Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) GN=NMA111 PE=3 SV=2 3 997 0.0E+00
sp|A6RG85|NM111_AJECN Pro-apoptotic serine protease NMA111 OS=Ajellomyces capsulatus (strain NAm1 / WU24) GN=NMA111 PE=3 SV=2 74 994 0.0E+00
sp|O74325|YH05_SCHPO PDZ domain-containing protein C1685.05 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1685.05 PE=4 SV=1 65 975 4.0E-142
sp|Q8RY22|DEGP7_ARATH Protease Do-like 7 OS=Arabidopsis thaliana GN=DEGP7 PE=2 SV=1 74 529 1.0E-106
sp|Q8RY22|DEGP7_ARATH Protease Do-like 7 OS=Arabidopsis thaliana GN=DEGP7 PE=2 SV=1 549 990 4.0E-53
sp|P72780|HHOA_SYNY3 Putative serine protease HhoA OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=hhoA PE=1 SV=1 103 394 1.0E-14
sp|E1V4H2|DEGPL_HALED Probable periplasmic serine endoprotease DegP-like OS=Halomonas elongata (strain ATCC 33173 / DSM 2581 / NBRC 15536 / NCIMB 2198 / 1H9) GN=mucD PE=3 SV=1 105 392 3.0E-12
sp|B1J4D7|DEGPL_PSEPW Probable periplasmic serine endoprotease DegP-like OS=Pseudomonas putida (strain W619) GN=PputW619_1070 PE=3 SV=1 105 474 8.0E-11
sp|Q2SL36|DEGPL_HAHCH Probable periplasmic serine endoprotease DegP-like OS=Hahella chejuensis (strain KCTC 2396) GN=mucD PE=3 SV=1 105 395 9.0E-11
sp|P0C0V0|DEGP_ECOLI Periplasmic serine endoprotease DegP OS=Escherichia coli (strain K12) GN=degP PE=1 SV=1 107 390 1.0E-10
sp|P0C0V1|DEGP_ECO57 Periplasmic serine endoprotease DegP OS=Escherichia coli O157:H7 GN=degP PE=3 SV=1 107 390 1.0E-10
sp|P26982|DEGP_SALTY Periplasmic serine endoprotease DegP OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=degP PE=3 SV=1 107 390 2.0E-10
sp|Q8YG32|DEGPL_BRUME Probable periplasmic serine endoprotease DegP-like OS=Brucella melitensis biotype 1 (strain 16M / ATCC 23456 / NCTC 10094) GN=htrA PE=3 SV=1 105 355 5.0E-10
sp|P0A3Z5|DEGPL_BRUSU Probable periplasmic serine endoprotease DegP-like OS=Brucella suis biovar 1 (strain 1330) GN=htrA PE=3 SV=1 105 355 5.0E-10
sp|P0C114|DEGPL_BRUAB Probable periplasmic serine endoprotease DegP-like OS=Brucella abortus biovar 1 (strain 9-941) GN=htrA PE=3 SV=1 105 355 5.0E-10
sp|Q2YMX6|DEGPL_BRUA2 Probable periplasmic serine endoprotease DegP-like OS=Brucella abortus (strain 2308) GN=htrA PE=3 SV=1 105 355 5.0E-10
sp|P54925|DEGPL_BARHE Probable periplasmic serine endoprotease DegP-like OS=Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) GN=htrA PE=3 SV=2 107 390 9.0E-10
sp|P39099|DEGQ_ECOLI Periplasmic pH-dependent serine endoprotease DegQ OS=Escherichia coli (strain K12) GN=degQ PE=1 SV=1 79 390 1.0E-09
sp|A6YFB5|HTRA1_XENLA Serine protease HTRA1 OS=Xenopus laevis GN=htra1 PE=1 SV=1 77 388 1.0E-09
sp|Q9PL97|DEGPL_CHLMU Probable periplasmic serine endoprotease DegP-like OS=Chlamydia muridarum (strain MoPn / Nigg) GN=htrA PE=3 SV=1 107 466 1.0E-09
sp|Q52894|DEGPL_RHIME Probable periplasmic serine endoprotease DegP-like OS=Rhizobium meliloti (strain 1021) GN=degP1 PE=3 SV=2 105 393 2.0E-09
sp|A4XSC0|DEGPL_PSEMY Probable periplasmic serine endoprotease DegP-like OS=Pseudomonas mendocina (strain ymp) GN=Pmen_1471 PE=3 SV=1 105 474 4.0E-09
sp|P18584|DEGPL_CHLTR Probable periplasmic serine endoprotease DegP-like OS=Chlamydia trachomatis (strain D/UW-3/Cx) GN=htrA PE=3 SV=2 107 390 4.0E-09
sp|Q9D236|HTRA3_MOUSE Serine protease HTRA3 OS=Mus musculus GN=Htra3 PE=1 SV=3 77 384 1.0E-08
sp|D3ZA76|HTRA3_RAT Serine protease HTRA3 OS=Rattus norvegicus GN=Htra3 PE=2 SV=1 77 384 1.0E-08
sp|P45129|HTOA_HAEIN Probable periplasmic serine protease do/HhoA-like OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=HI_1259 PE=3 SV=1 107 392 1.0E-08
sp|Q9R9I1|HTRB_BACSU Serine protease Do-like HtrB OS=Bacillus subtilis (strain 168) GN=htrB PE=2 SV=1 110 382 2.0E-08
sp|Q48EU9|DEGPL_PSE14 Probable periplasmic serine endoprotease DegP-like OS=Pseudomonas savastanoi pv. phaseolicola (strain 1448A / Race 6) GN=mucD PE=3 SV=1 105 469 3.0E-08
sp|A4IHA1|HTRA1_XENTR Serine protease HTRA1 OS=Xenopus tropicalis GN=htra1 PE=2 SV=2 77 388 5.0E-08
sp|Q89AP5|DEGPL_BUCBP Probable periplasmic serine endoprotease DegP-like OS=Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) GN=htrA PE=3 SV=1 74 469 6.0E-08
sp|A9JRB3|HTR1B_DANRE Serine protease HTRA1B OS=Danio rerio GN=htra1b PE=2 SV=1 77 384 6.0E-08
sp|P39668|YYXA_BACSU Uncharacterized serine protease YyxA OS=Bacillus subtilis (strain 168) GN=yyxA PE=3 SV=2 76 390 9.0E-08
sp|P05676|Y938_SYNP6 Uncharacterized serine protease syc0938_d OS=Synechococcus sp. (strain ATCC 27144 / PCC 6301 / SAUG 1402/1) GN=syc0938_d PE=3 SV=2 106 395 1.0E-07
sp|Q9Z6T0|DEGPL_CHLPN Probable periplasmic serine endoprotease DegP-like OS=Chlamydia pneumoniae GN=htrA PE=3 SV=1 107 466 3.0E-07
sp|Q9Z4H7|HTRA_LACHE Serine protease Do-like HtrA OS=Lactobacillus helveticus GN=htrA PE=3 SV=2 105 390 3.0E-07
sp|P83105|HTRA4_HUMAN Serine protease HTRA4 OS=Homo sapiens GN=HTRA4 PE=2 SV=1 79 367 3.0E-06
sp|Q9JIY5|HTRA2_MOUSE Serine protease HTRA2, mitochondrial OS=Mus musculus GN=Htra2 PE=1 SV=2 77 357 3.0E-06
sp|A2RT60|HTRA4_MOUSE Serine protease HTRA4 OS=Mus musculus GN=Htra4 PE=2 SV=1 79 356 4.0E-06
sp|A0JNK3|HTRA2_BOVIN Serine protease HTRA2, mitochondrial OS=Bos taurus GN=HTRA2 PE=2 SV=1 77 355 6.0E-06
sp|D3ZKF5|HTRA4_RAT Serine protease HTR4 OS=Rattus norvegicus GN=Htra4 PE=3 SV=1 79 356 8.0E-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
Nucleus Nuclear localization signal 0.4331 0.7196 0.1994 0.0845 0.0836 0.0622 0.1771 0.055 0.139 0.0033

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
Orthogroup2476
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|5807
Ophiocordyceps australis map64 (Brazil) OphauB2|2740
Ophiocordyceps camponoti-floridani Ophcf2|04028
Ophiocordyceps camponoti-rufipedis Ophun1|474
Ophiocordyceps kimflemingae Ophio5|3961
Ophiocordyceps subramaniannii Hirsu2|3575 (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|3575
MNGSRPANAGKRKAPASPAPAPPAKRSVNGKLPPADDDDDSVEYDDDDGGDSCLSDDLHGHDALYIGTPGSLGEW
QDTIQKVVRNVVAIRFCQTCSFDTDPALTSEATGFVVDSERGYIMTNRHVVGAGPFWGHCVFDNHEEVDCYPVYR
DPVHDFGILRYDPKAIKYMHVDGLDIRPEQAKVGVEIRVVGNDAGEKLSILSGVISRLDRNAPEYGEGYCDFNTC
YYQANAAACGGSSGSPVVSKDGSAIALQAGGRSDGASTDYFLPLDRPLRALQCIQQGQPITRGDIQCQFLLKPFD
ECRRLGLSPHWEAATREAFPNETNMLVAEIVLPSGPSHNKMEEGDVLIKVNGELITQFIRLDEILDSSVGKPVKL
QLQRGGQDVEVEVEVGDLHAITPDRFVSVAGASFHNLSYQQARLYAVQLKGVYVCESAGSFRFDTTDNGWIIQTV
DHKKVPDLDTFIDVMKKIPDKARVVVTYKHLRDLHTLNTTVIYVDRHWSSKMKLAVRNDATGLWDFSDLGDPLPP
VPPVRRSASFIELDHMPHPGIADLIRSFVHVNCTMPVKLDGFPKNRRWGMGLVIDAEKGLVLISRAIVPYDLCDI
TVTIADSVIVEAKVVFLHPLQNYVIIKYDPSLVDAPVKSARMSDEHLTQGAKTYFLGYNRIGRVVHGATTVTEIT
AVAIPANSGAPRYRAVNVDAITIDSNLGSSCNSGVLVSPDGTVQALWLSYLGERSPCSQRDEEYYLGLGTPTLLP
VIAAVQRGETPQLRMLSVEFRSVQMSQARVMGVSDEWIKKVTQANRSHHQLFMVSKRTFERGEHPVSLLEGDIVL
TLNGKICTTISDFDVMYTSEVLDAVIVRECEELQLQLPTVAANDMETDHAVSFCGAVLHRPHQAVRQQISKLHSE
VYVSSRIRGSPAYQYGVAPTNFITHVNGQPTPDLNSFIAATRRIPDNTYFRLKAVTFDSVPWVITMKKNDHYFPT
MEWIKDGSEACGWRRVTYEGMDVFQGEAPDGLPPVVEDAEME*
Coding >Hirsu2|3575
ATGAACGGCTCTCGACCCGCCAACGCCGGCAAGAGAAAAGCCCCGGCGTCGCCGGCCCCGGCACCGCCCGCCAAG
CGCTCCGTCAATGGCAAGCTCCCCCCCGCCGACGATGACGACGACAGCGTCGAGTACGACGACGACGACGGCGGC
GACTCCTGTCTCTCCGACGACCTCCACGGCCACGACGCCCTGTATATCGGCACGCCAGGCAGCCTGGGAGAGTGG
CAAGATACCATCCAGAAGGTGGTCCGCAATGTCGTCGCCATCCGCTTCTGCCAGACCTGTTCCTTCGACACCGAT
CCCGCCTTGACGAGCGAGGCGACCGGCTTCGTCGTCGACTCCGAACGGGGCTACATCATGACGAATCGACACGTC
GTCGGCGCCGGTCCCTTTTGGGGTCACTGCGTCTTCGACAACCACGAGGAGGTCGACTGCTATCCCGTCTACCGC
GACCCCGTCCACGATTTCGGCATCCTCCGCTACGACCCCAAAGCAATCAAGTATATGCACGTCGATGGCCTGGAC
ATCCGGCCGGAGCAGGCCAAGGTCGGCGTCGAGATTCGCGTCGTGGGAAACGACGCCGGCGAGAAGCTCAGCATC
TTGTCGGGCGTCATCAGCCGCCTCGACCGAAACGCCCCCGAGTACGGCGAAGGCTACTGCGATTTCAACACGTGC
TACTACCAGGCAAACGCCGCCGCATGTGGCGGTAGCTCCGGCAGTCCGGTCGTGAGCAAGGACGGCTCCGCCATC
GCCCTGCAGGCTGGCGGCCGCTCGGACGGGGCCTCGACCGACTACTTCCTCCCCCTCGATCGCCCCTTGCGCGCC
CTGCAGTGCATCCAGCAGGGACAGCCCATCACCCGCGGCGACATCCAGTGCCAGTTCCTGCTCAAGCCGTTCGAC
GAATGCCGTAGGCTCGGCCTCTCCCCCCACTGGGAGGCCGCCACGCGCGAGGCCTTTCCGAACGAGACAAACATG
CTCGTCGCCGAGATCGTCCTGCCCTCGGGCCCCTCGCACAACAAGATGGAGGAGGGAGACGTCCTCATCAAGGTC
AACGGCGAGCTCATCACCCAATTCATCCGCTTGGACGAGATCCTCGACTCGAGCGTCGGCAAGCCCGTCAAGCTC
CAGCTGCAGCGAGGCGGCCAGGACGTCGAGGTGGAGGTGGAGGTCGGCGACCTGCACGCCATCACGCCCGACCGC
TTCGTCTCCGTCGCGGGCGCCAGCTTCCACAACCTCTCCTACCAGCAGGCCAGGCTGTACGCGGTCCAGCTCAAG
GGCGTCTACGTCTGCGAGTCGGCCGGCTCCTTCAGGTTCGACACGACCGACAACGGGTGGATCATACAGACCGTC
GACCACAAGAAGGTGCCCGATCTCGACACCTTCATCGACGTCATGAAGAAGATACCGGACAAGGCCCGCGTCGTC
GTCACCTACAAGCACCTGCGGGACCTGCACACCCTCAACACGACCGTCATCTACGTCGACCGCCACTGGTCCTCC
AAGATGAAGCTGGCGGTGCGCAACGACGCGACGGGCCTGTGGGACTTTTCCGACCTGGGCGACCCGCTGCCGCCC
GTGCCGCCCGTCCGCCGCTCGGCCTCGTTCATCGAGCTCGACCACATGCCGCATCCGGGCATCGCCGACCTGATC
CGAAGCTTCGTCCACGTCAACTGCACCATGCCCGTCAAGCTCGACGGCTTCCCCAAGAACCGGCGCTGGGGCATG
GGCCTGGTCATCGACGCCGAGAAGGGCCTGGTGCTCATCTCGCGGGCCATCGTGCCCTACGACCTGTGCGACATC
ACCGTCACCATCGCCGACTCCGTCATCGTCGAGGCCAAGGTCGTCTTCCTGCACCCGCTGCAAAACTACGTCATC
ATCAAGTACGACCCGTCGCTCGTGGACGCGCCCGTCAAGAGCGCCAGGATGAGCGACGAGCACCTCACCCAGGGC
GCCAAGACGTACTTCCTCGGCTACAATAGGATCGGCCGCGTCGTCCACGGCGCCACCACCGTGACCGAGATCACG
GCCGTCGCCATCCCGGCCAACTCGGGGGCGCCGCGATACCGGGCCGTCAACGTCGACGCCATCACCATCGACAGC
AACCTCGGCTCCTCGTGCAACAGCGGCGTCCTCGTGTCCCCCGACGGGACCGTGCAGGCGCTCTGGCTCTCGTAC
CTGGGCGAGCGGTCGCCGTGCAGCCAGCGAGACGAGGAGTACTACCTGGGCCTGGGCACGCCGACGCTGCTGCCC
GTCATCGCGGCCGTCCAGAGGGGCGAGACGCCGCAGCTGCGCATGCTGTCCGTCGAGTTCCGGTCCGTGCAGATG
TCGCAGGCCCGCGTCATGGGCGTGTCGGACGAGTGGATCAAGAAGGTGACGCAGGCGAACCGGTCGCACCACCAG
CTCTTCATGGTCAGCAAGCGGACGTTTGAGCGCGGCGAACACCCGGTGTCCCTCCTCGAGGGCGACATCGTGCTG
ACGCTCAACGGCAAGATTTGCACCACCATCTCCGACTTCGATGTCATGTACACCAGCGAGGTGTTGGATGCCGTC
ATCGTCCGCGAGTGCGAGGAGCTGCAGCTGCAGCTGCCGACGGTCGCCGCCAACGACATGGAGACGGACCACGCC
GTCTCCTTTTGCGGCGCCGTCCTCCACCGCCCGCACCAAGCGGTGCGCCAGCAGATCAGCAAGCTGCACAGCGAG
GTTTACGTGTCCAGCCGGATCCGCGGCTCGCCGGCCTATCAGTATGGCGTTGCGCCAACTAACTTCATCACGCAC
GTCAACGGCCAGCCGACGCCGGACCTCAACTCGTTCATCGCCGCGACGCGGAGGATCCCGGATAACACCTATTTT
CGCCTCAAGGCGGTCACGTTCGACAGCGTGCCGTGGGTGATTACGATGAAGAAGAACGACCACTACTTCCCCACC
ATGGAATGGATCAAGGACGGCAGCGAAGCCTGCGGGTGGCGGCGCGTGACGTACGAGGGCATGGACGTGTTCCAG
GGCGAGGCCCCCGACGGGCTGCCACCGGTGGTGGAGGACGCGGAGATGGAGTAG
Transcript >Hirsu2|3575
ATGAACGGCTCTCGACCCGCCAACGCCGGCAAGAGAAAAGCCCCGGCGTCGCCGGCCCCGGCACCGCCCGCCAAG
CGCTCCGTCAATGGCAAGCTCCCCCCCGCCGACGATGACGACGACAGCGTCGAGTACGACGACGACGACGGCGGC
GACTCCTGTCTCTCCGACGACCTCCACGGCCACGACGCCCTGTATATCGGCACGCCAGGCAGCCTGGGAGAGTGG
CAAGATACCATCCAGAAGGTGGTCCGCAATGTCGTCGCCATCCGCTTCTGCCAGACCTGTTCCTTCGACACCGAT
CCCGCCTTGACGAGCGAGGCGACCGGCTTCGTCGTCGACTCCGAACGGGGCTACATCATGACGAATCGACACGTC
GTCGGCGCCGGTCCCTTTTGGGGTCACTGCGTCTTCGACAACCACGAGGAGGTCGACTGCTATCCCGTCTACCGC
GACCCCGTCCACGATTTCGGCATCCTCCGCTACGACCCCAAAGCAATCAAGTATATGCACGTCGATGGCCTGGAC
ATCCGGCCGGAGCAGGCCAAGGTCGGCGTCGAGATTCGCGTCGTGGGAAACGACGCCGGCGAGAAGCTCAGCATC
TTGTCGGGCGTCATCAGCCGCCTCGACCGAAACGCCCCCGAGTACGGCGAAGGCTACTGCGATTTCAACACGTGC
TACTACCAGGCAAACGCCGCCGCATGTGGCGGTAGCTCCGGCAGTCCGGTCGTGAGCAAGGACGGCTCCGCCATC
GCCCTGCAGGCTGGCGGCCGCTCGGACGGGGCCTCGACCGACTACTTCCTCCCCCTCGATCGCCCCTTGCGCGCC
CTGCAGTGCATCCAGCAGGGACAGCCCATCACCCGCGGCGACATCCAGTGCCAGTTCCTGCTCAAGCCGTTCGAC
GAATGCCGTAGGCTCGGCCTCTCCCCCCACTGGGAGGCCGCCACGCGCGAGGCCTTTCCGAACGAGACAAACATG
CTCGTCGCCGAGATCGTCCTGCCCTCGGGCCCCTCGCACAACAAGATGGAGGAGGGAGACGTCCTCATCAAGGTC
AACGGCGAGCTCATCACCCAATTCATCCGCTTGGACGAGATCCTCGACTCGAGCGTCGGCAAGCCCGTCAAGCTC
CAGCTGCAGCGAGGCGGCCAGGACGTCGAGGTGGAGGTGGAGGTCGGCGACCTGCACGCCATCACGCCCGACCGC
TTCGTCTCCGTCGCGGGCGCCAGCTTCCACAACCTCTCCTACCAGCAGGCCAGGCTGTACGCGGTCCAGCTCAAG
GGCGTCTACGTCTGCGAGTCGGCCGGCTCCTTCAGGTTCGACACGACCGACAACGGGTGGATCATACAGACCGTC
GACCACAAGAAGGTGCCCGATCTCGACACCTTCATCGACGTCATGAAGAAGATACCGGACAAGGCCCGCGTCGTC
GTCACCTACAAGCACCTGCGGGACCTGCACACCCTCAACACGACCGTCATCTACGTCGACCGCCACTGGTCCTCC
AAGATGAAGCTGGCGGTGCGCAACGACGCGACGGGCCTGTGGGACTTTTCCGACCTGGGCGACCCGCTGCCGCCC
GTGCCGCCCGTCCGCCGCTCGGCCTCGTTCATCGAGCTCGACCACATGCCGCATCCGGGCATCGCCGACCTGATC
CGAAGCTTCGTCCACGTCAACTGCACCATGCCCGTCAAGCTCGACGGCTTCCCCAAGAACCGGCGCTGGGGCATG
GGCCTGGTCATCGACGCCGAGAAGGGCCTGGTGCTCATCTCGCGGGCCATCGTGCCCTACGACCTGTGCGACATC
ACCGTCACCATCGCCGACTCCGTCATCGTCGAGGCCAAGGTCGTCTTCCTGCACCCGCTGCAAAACTACGTCATC
ATCAAGTACGACCCGTCGCTCGTGGACGCGCCCGTCAAGAGCGCCAGGATGAGCGACGAGCACCTCACCCAGGGC
GCCAAGACGTACTTCCTCGGCTACAATAGGATCGGCCGCGTCGTCCACGGCGCCACCACCGTGACCGAGATCACG
GCCGTCGCCATCCCGGCCAACTCGGGGGCGCCGCGATACCGGGCCGTCAACGTCGACGCCATCACCATCGACAGC
AACCTCGGCTCCTCGTGCAACAGCGGCGTCCTCGTGTCCCCCGACGGGACCGTGCAGGCGCTCTGGCTCTCGTAC
CTGGGCGAGCGGTCGCCGTGCAGCCAGCGAGACGAGGAGTACTACCTGGGCCTGGGCACGCCGACGCTGCTGCCC
GTCATCGCGGCCGTCCAGAGGGGCGAGACGCCGCAGCTGCGCATGCTGTCCGTCGAGTTCCGGTCCGTGCAGATG
TCGCAGGCCCGCGTCATGGGCGTGTCGGACGAGTGGATCAAGAAGGTGACGCAGGCGAACCGGTCGCACCACCAG
CTCTTCATGGTCAGCAAGCGGACGTTTGAGCGCGGCGAACACCCGGTGTCCCTCCTCGAGGGCGACATCGTGCTG
ACGCTCAACGGCAAGATTTGCACCACCATCTCCGACTTCGATGTCATGTACACCAGCGAGGTGTTGGATGCCGTC
ATCGTCCGCGAGTGCGAGGAGCTGCAGCTGCAGCTGCCGACGGTCGCCGCCAACGACATGGAGACGGACCACGCC
GTCTCCTTTTGCGGCGCCGTCCTCCACCGCCCGCACCAAGCGGTGCGCCAGCAGATCAGCAAGCTGCACAGCGAG
GTTTACGTGTCCAGCCGGATCCGCGGCTCGCCGGCCTATCAGTATGGCGTTGCGCCAACTAACTTCATCACGCAC
GTCAACGGCCAGCCGACGCCGGACCTCAACTCGTTCATCGCCGCGACGCGGAGGATCCCGGATAACACCTATTTT
CGCCTCAAGGCGGTCACGTTCGACAGCGTGCCGTGGGTGATTACGATGAAGAAGAACGACCACTACTTCCCCACC
ATGGAATGGATCAAGGACGGCAGCGAAGCCTGCGGGTGGCGGCGCGTGACGTACGAGGGCATGGACGTGTTCCAG
GGCGAGGCCCCCGACGGGCTGCCACCGGTGGTGGAGGACGCGGAGATGGAGTAG
Gene >Hirsu2|3575
ATGAACGGCTCTCGACCCGCCAACGCCGGCAAGAGAAAAGCCCCGGCGTCGCCGGCCCCGGCACCGCCCGCCAAG
CGCTCCGTCAATGGCAAGCTCCCCCCCGCCGACGATGACGACGACAGCGTCGAGTACGACGACGACGACGGCGGC
GACTCCTGTCTCTCCGACGACCTCCACGGCCACGACGCCCTGTATATCGGCACGCCAGGCAGCCTGGGAGAGTGG
CAAGATACCATCCAGAAGGTGGTCCGCAATGTCGTCGCCATCCGCTTCTGCCAGACCTGTTCCTTCGACACCGAT
CCCGCCTTGACGAGCGAGGCGACCGGCTTCGTCGTCGACTCCGAACGGGGGTAAGTGGCCTCCCCCCCCCCTTGT
CTCCGACCTATGCCGGGCTGGACGACGTGCTGACCTGCTTGCAGCTACATCATGACGAATCGACACGTCGTCGGC
GCCGGTCCCTTTTGGGGTCACTGCGTCTTCGACAACCACGAGGAGGTCGACTGCTATCCCGTCTACCGCGACCCC
GTCCACGATTTCGGCATCCTCCGCTACGACCCCAAAGCAATCAAGTATATGCACGTCGATGGCCTGGACATCCGG
CCGGAGCAGGCCAAGGGTACGCCTCCAACCCCCCCCCCCCCCCCCCCCCCCCCCTTCTCCCTCCTCCGTCTTGGC
CGGACCTCGCAGCTGACGCATAGTCATCAGTCGGCGTCGAGATTCGCGTCGTGGGAAACGACGCCGGCGAGAAGC
TCAGCATCTTGTCGGGCGTCATCAGCCGCCTCGACCGAAACGCCCCCGAGTACGGCGAAGGCTACTGCGATTTCA
ACACGTGCTACTACCAGGCAAACGCCGCCGCATGTGGCGGTAGCTCCGGCAGTCCGGTCGTGAGCAAGGACGGCT
CCGCCATCGCCCTGCAGGCTGGCGGCCGCTCGGACGGGGCCTCGACCGACTACTTCCTCCCCCTCGATCGCCCCT
TGCGCGCCCTGCAGTGCATCCAGCAGGGACAGCCCATCACCCGCGGCGACATCCAGTGCCAGTTCCTGCTCAAGC
CGTTCGACGAATGCCGTAGGCTCGGCCTCTCCCCCCACTGGGAGGCCGCCACGCGCGAGGCCTTTCCGAACGAGA
CAAACATGCTCGTCGCCGAGATCGTCCTGCCCTCGGGCCCCTCGCACAACAAGATGGAGGAGGGAGACGTCCTCA
TCAAGGTCAACGGCGAGCTCATCACCCAATTCATCCGCTTGGACGAGATCCTCGACTCGAGCGTCGGCAAGCCCG
TCAAGCTCCAGCTGCAGCGAGGCGGCCAGGACGTCGAGGTGGAGGTGGAGGTCGGCGACCTGCACGCCATCACGC
CCGACCGCTTCGTCTCCGTCGCGGGCGCCAGCTTCCACAACCTCTCCTACCAGCAGGCCAGGCTGTACGCGGTCC
AGCTCAAGGGCGTCTACGTCTGCGAGTCGGCCGGCTCCTTCAGGTTCGACACGACCGACAACGGGTGGATCATAC
AGACCGTCGACCACAAGAAGGTGCCCGATCTCGACACCTTCATCGACGTCATGAAGAAGATACCGGACAAGGCCC
GCGTCGTCGTCACCTACAAGCACCTGCGGGACCTGCACACCCTCAACACGACCGTCATCTACGTCGACCGCCACT
GGTCCTCCAAGATGAAGCTGGCGGTGCGCAACGACGCGACGGGCCTGTGGGACTTTTCCGACCTGGGCGACCCGC
TGCCGCCCGTGCCGCCCGTCCGCCGCTCGGCCTCGTTCATCGAGCTCGACCACATGCCGCATCCGGGCATCGCCG
ACCTGATCCGAAGCTTCGTCCACGTCAACTGCACCATGCCCGTCAAGCTCGACGGCTTCCCCAAGAACCGGCGCT
GGGGCATGGGCCTGGTCATCGACGCCGAGAAGGGCCTGGTGCTCATCTCGCGGGCCATCGTGCCCTACGACCTGT
GCGACATCACCGTCACCATCGCCGACTCCGTCATCGTCGAGGCCAAGGTCGTCTTCCTGCACCCGCTGCAAAACT
ACGTCATCATCAAGTACGACCCGTCGCTCGTGGACGCGCCCGTCAAGAGCGCCAGGATGAGCGACGAGCACCTCA
CCCAGGGCGCCAAGACGTACTTCCTCGGCTACAATAGGATCGGCCGCGTCGTCCACGGCGCCACCACCGTGACCG
AGATCACGGCCGTCGCCATCCCGGCCAACTCGGGGGCGCCGCGATACCGGGCCGTCAACGTCGACGCCATCACCA
TCGACAGCAACCTCGGCTCCTCGTGCAACAGCGGCGTCCTCGTGTCCCCCGACGGGACCGTGCAGGCGCTCTGGC
TCTCGTACCTGGGCGAGCGGTCGCCGTGCAGCCAGCGAGACGAGGAGTACTACCTGGGCCTGGGCACGCCGACGC
TGCTGCCCGTCATCGCGGCCGTCCAGAGGGGCGAGACGCCGCAGCTGCGCATGCTGTCCGTCGAGTTCCGGTCCG
TGCAGATGTCGCAGGCCCGCGTCATGGGCGTGTCGGACGAGTGGATCAAGAAGGTGACGCAGGCGAACCGGTCGC
ACCACCAGCTCTTCATGGTCAGCAAGCGGACGTTTGAGCGCGGCGAACACCCGGTGTCCCTCCTCGAGGGCGACA
TCGTGCTGACGCTCAACGGCAAGATTTGCACCACCATCTCCGACTTCGATGTCATGTACACCAGCGAGGTGTTGG
ATGCCGTCATCGTCCGCGAGTGCGAGGAGCTGCAGCTGCAGCTGCCGACGGTCGCCGCCAACGACATGGAGACGG
ACCACGCCGTCTCCTTTTGCGGCGCCGTCCTCCACCGCCCGCACCAAGCGGTGCGCCAGCAGATCAGCAAGCTGC
ACAGCGAGGTTTACGTGTCCAGCCGGATCCGCGGCTCGCCGGCCTATCAGTATGGCGTTGCGCCAACTAACTTCA
TCACGCACGTCAACGGCCAGCCGACGCCGGACCTCAACTCGTTCATCGCCGCGACGCGGAGGATCCCGGATAACA
CCTGTAAGTTGACACCCCGAAGCGGCAAGACGGGCGTCTCGGGAGCTGACATGAATGGCCGTCAGATTTTCGCCT
CAAGGCGGTCACGTTCGACAGCGTGCCGTGGGTGATTACGATGAAGAAGAACGACCACTACTTCCCCACCATGGA
ATGGATCAAGGACGGCAGCGAAGCCTGCGGGTGGCGGCGCGTGACGTACGAGGGCATGGACGTGTTCCAGGGCGA
GGCCCCCGACGGGCTGCCACCGGTGGTGGAGGACGCGGAGATGGAGTAG

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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