© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|10166 |
| Gene name | |
| Location | Contig_8:27772..31461 |
| Strand | + |
| Gene length (bp) | 3689 |
| Transcript length (bp) | 3570 |
| Coding sequence length (bp) | 3570 |
| Protein length (aa) | 1190 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00368 | HMG-CoA_red | Hydroxymethylglutaryl-coenzyme A reductase | 9.0E-139 | 761 | 1144 |
| PF13323 | HPIH | N-terminal domain with HPIH motif | 4.0E-48 | 30 | 174 |
| PF12349 | Sterol-sensing | Sterol-sensing domain of SREBP cleavage-activation | 5.9E-14 | 265 | 427 |
| PF02460 | Patched | Patched family | 1.4E-08 | 240 | 437 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P0CT44|HMDH_GIBFU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Gibberella fujikuroi GN=HMGR PE=3 SV=1 | 218 | 1155 | 0.0E+00 |
| sp|S0DQM8|HMDH_GIBF5 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Gibberella fujikuroi (strain CBS 195.34 / IMI 58289 / NRRL A-6831) GN=HMGR PE=3 SV=1 | 6 | 1189 | 0.0E+00 |
| sp|P12684|HMDH2_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG2 PE=1 SV=1 | 598 | 1161 | 0.0E+00 |
| sp|O74164|HMDH_CYBJA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Cyberlindnera jadinii GN=HMG PE=2 SV=1 | 224 | 1147 | 0.0E+00 |
| sp|P12683|HMDH1_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG1 PE=1 SV=1 | 216 | 1147 | 0.0E+00 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P0CT44|HMDH_GIBFU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Gibberella fujikuroi GN=HMGR PE=3 SV=1 | 218 | 1155 | 0.0E+00 |
| sp|S0DQM8|HMDH_GIBF5 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Gibberella fujikuroi (strain CBS 195.34 / IMI 58289 / NRRL A-6831) GN=HMGR PE=3 SV=1 | 6 | 1189 | 0.0E+00 |
| sp|P12684|HMDH2_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG2 PE=1 SV=1 | 598 | 1161 | 0.0E+00 |
| sp|O74164|HMDH_CYBJA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Cyberlindnera jadinii GN=HMG PE=2 SV=1 | 224 | 1147 | 0.0E+00 |
| sp|P12683|HMDH1_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG1 PE=1 SV=1 | 216 | 1147 | 0.0E+00 |
| sp|Q10283|HMDH_SCHPO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=hmg1 PE=1 SV=2 | 215 | 1151 | 0.0E+00 |
| sp|Q9Y7D2|HMDH_ASPTE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Aspergillus terreus PE=3 SV=2 | 24 | 1149 | 0.0E+00 |
| sp|Q0C8L9|HMDH_ASPTN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=ATEG_09965 PE=3 SV=1 | 19 | 1149 | 0.0E+00 |
| sp|Q12649|HMDH_PHYB8 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Phycomyces blakesleeanus (strain ATCC 8743b / FGSC 10004 / NBRC 33097 / NRRL 1555) GN=hmgA PE=3 SV=2 | 227 | 1160 | 0.0E+00 |
| sp|Q01237|HMDH_MOUSE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Mus musculus GN=Hmgcr PE=1 SV=3 | 712 | 1145 | 2.0E-155 |
| sp|Q5R6N3|HMDH_PONAB | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Pongo abelii GN=HMGCR PE=2 SV=1 | 712 | 1145 | 1.0E-154 |
| sp|A7Z064|HMDH_BOVIN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Bos taurus GN=HMGCR PE=2 SV=2 | 712 | 1145 | 1.0E-154 |
| sp|P04035|HMDH_HUMAN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Homo sapiens GN=HMGCR PE=1 SV=1 | 712 | 1145 | 1.0E-154 |
| sp|P00347|HMDH_CRIGR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Cricetulus griseus GN=HMGCR PE=1 SV=1 | 711 | 1145 | 8.0E-154 |
| sp|Q9XHL5|HMDH3_ORYSJ | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 3 OS=Oryza sativa subsp. japonica GN=HMG3 PE=2 SV=2 | 733 | 1146 | 1.0E-153 |
| sp|O24594|HMDH_MAIZE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Zea mays GN=HMGR PE=3 SV=1 | 725 | 1146 | 1.0E-153 |
| sp|P20715|HMDH_XENLA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Xenopus laevis GN=hmgcr PE=2 SV=1 | 712 | 1145 | 1.0E-153 |
| sp|P09610|HMDH_MESAU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Mesocricetus auratus GN=HMGCR PE=1 SV=1 | 711 | 1145 | 3.0E-153 |
| sp|P51639|HMDH_RAT | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Rattus norvegicus GN=Hmgcr PE=1 SV=2 | 711 | 1145 | 1.0E-152 |
| sp|Q01559|HMDH_NICSY | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Nicotiana sylvestris GN=HMGR PE=2 SV=1 | 733 | 1145 | 3.0E-152 |
| sp|P54960|HMDH_BLAGE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Blattella germanica PE=2 SV=1 | 711 | 1155 | 9.0E-152 |
| sp|Q1W675|HMDH_PIG | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Sus scrofa GN=HMGCR PE=2 SV=1 | 711 | 1145 | 1.0E-151 |
| sp|Q29512|HMDH_RABIT | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Oryctolagus cuniculus GN=HMGCR PE=3 SV=1 | 712 | 1145 | 2.0E-151 |
| sp|Q9XEL8|HMDH2_CAPAN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Capsicum annuum GN=HMGR2 PE=2 SV=1 | 733 | 1145 | 7.0E-151 |
| sp|P34136|HMDH2_DICDI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Dictyostelium discoideum GN=hmgB PE=2 SV=2 | 730 | 1158 | 1.0E-150 |
| sp|P29057|HMDH1_HEVBR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Hevea brasiliensis GN=HMGR1 PE=2 SV=1 | 733 | 1146 | 2.0E-150 |
| sp|P16393|HMDH_STRPU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Strongylocentrotus purpuratus GN=HMGCR PE=2 SV=2 | 714 | 1146 | 2.0E-150 |
| sp|P48022|HMDH2_SOLLC | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Solanum lycopersicum GN=HMG2 PE=3 SV=1 | 733 | 1145 | 3.0E-150 |
| sp|O64967|HMDH2_GOSHI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Gossypium hirsutum GN=HMG2 PE=3 SV=1 | 658 | 1146 | 3.0E-150 |
| sp|O64966|HMDH1_GOSHI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Gossypium hirsutum GN=HMG1 PE=3 SV=1 | 686 | 1144 | 4.0E-150 |
| sp|Q03163|HMDH_CATRO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Catharanthus roseus GN=HMGR PE=2 SV=1 | 733 | 1146 | 5.0E-150 |
| sp|P48020|HMDH1_SOLTU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Solanum tuberosum GN=HMG1 PE=2 SV=1 | 631 | 1145 | 3.0E-149 |
| sp|P48021|HMDH_CAMAC | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Camptotheca acuminata PE=3 SV=1 | 733 | 1145 | 6.0E-148 |
| sp|Q41438|HMDH3_SOLTU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 3 OS=Solanum tuberosum GN=HMG3 PE=2 SV=1 | 723 | 1146 | 3.0E-147 |
| sp|Q41437|HMDH2_SOLTU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Solanum tuberosum GN=HMG2 PE=2 SV=1 | 733 | 1149 | 7.0E-147 |
| sp|P14891|HMDH1_ARATH | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Arabidopsis thaliana GN=HMG1 PE=1 SV=1 | 733 | 1146 | 3.0E-146 |
| sp|P34135|HMDH1_DICDI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Dictyostelium discoideum GN=hmgA PE=2 SV=1 | 730 | 1145 | 8.0E-146 |
| sp|Q00583|HMDH3_HEVBR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 3 OS=Hevea brasiliensis GN=HMGR3 PE=2 SV=1 | 734 | 1146 | 8.0E-145 |
| sp|P43256|HMDH2_ARATH | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Arabidopsis thaliana GN=HMG2 PE=2 SV=1 | 725 | 1146 | 1.0E-144 |
| sp|Q0DY59|HMDH1_ORYSJ | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Oryza sativa subsp. japonica GN=HMG1 PE=2 SV=2 | 733 | 1146 | 2.0E-139 |
| sp|A2X8W3|HMDH1_ORYSI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Oryza sativa subsp. indica GN=HMG1 PE=2 SV=2 | 733 | 1146 | 4.0E-139 |
| sp|P14773|HMDH_DROME | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Drosophila melanogaster GN=Hmgcr PE=2 SV=2 | 731 | 1154 | 3.0E-135 |
| sp|O76819|HMDH_AGRIP | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Agrotis ipsilon GN=HMGR PE=2 SV=1 | 699 | 1145 | 2.0E-130 |
| sp|P16237|HMDH_SCHMA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Schistosoma mansoni PE=2 SV=1 | 718 | 1160 | 1.0E-110 |
| sp|O59469|HMDH_PYRHO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) GN=hmgA PE=3 SV=2 | 730 | 1144 | 5.0E-99 |
| sp|Q9V1R3|HMDH_PYRAB | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Pyrococcus abyssi (strain GE5 / Orsay) GN=hmgA PE=3 SV=2 | 731 | 1144 | 2.0E-97 |
| sp|O26662|HMDH_METTH | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) GN=hmgA PE=3 SV=1 | 741 | 1144 | 6.0E-91 |
| sp|Q59468|HMDH_HALVD | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Haloferax volcanii (strain ATCC 29605 / DSM 3757 / JCM 8879 / NBRC 14742 / NCIMB 2012 / VKM B-1768 / DS2) GN=hmgA PE=1 SV=2 | 731 | 1144 | 5.0E-87 |
| sp|Q9YAS4|HMDH_AERPE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) GN=hmgA PE=3 SV=1 | 734 | 1139 | 2.0E-81 |
| sp|O08424|HMDH_SULSO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Sulfolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) GN=hmgA PE=1 SV=2 | 731 | 1145 | 3.0E-81 |
| sp|Q58116|HMDH_METJA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=hmgA PE=3 SV=1 | 735 | 1144 | 8.0E-80 |
| sp|P29058|HMDH2_HEVBR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 (Fragment) OS=Hevea brasiliensis GN=HMGR2 PE=2 SV=1 | 948 | 1146 | 2.0E-77 |
| sp|B0R6J9|HMDH_HALS3 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) GN=hmgA PE=1 SV=1 | 802 | 1144 | 2.0E-76 |
| sp|P12684|HMDH2_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG2 PE=1 SV=1 | 39 | 452 | 2.0E-28 |
| sp|P14773|HMDH_DROME | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Drosophila melanogaster GN=Hmgcr PE=2 SV=2 | 223 | 493 | 1.0E-08 |
| sp|O28538|HMDH_ARCFU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Archaeoglobus fulgidus (strain ATCC 49558 / VC-16 / DSM 4304 / JCM 9628 / NBRC 100126) GN=hmgA PE=3 SV=1 | 802 | 1147 | 5.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0004420 | hydroxymethylglutaryl-CoA reductase (NADPH) activity | Yes |
| GO:0015936 | coenzyme A metabolic process | Yes |
| GO:0016021 | integral component of membrane | Yes |
| GO:0008152 | metabolic process | No |
| GO:1901360 | organic cyclic compound metabolic process | No |
| GO:0009987 | cellular process | No |
| GO:0019693 | ribose phosphate metabolic process | No |
| GO:0006139 | nucleobase-containing compound metabolic process | No |
| GO:0019637 | organophosphate metabolic process | No |
| GO:0031224 | intrinsic component of membrane | No |
| GO:0034641 | cellular nitrogen compound metabolic process | No |
| GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | No |
| GO:1901135 | carbohydrate derivative metabolic process | No |
| GO:0009259 | ribonucleotide metabolic process | No |
| GO:0033875 | ribonucleoside bisphosphate metabolic process | No |
| GO:0071704 | organic substance metabolic process | No |
| GO:0006753 | nucleoside phosphate metabolic process | No |
| GO:0006793 | phosphorus metabolic process | No |
| GO:0003824 | catalytic activity | No |
| GO:0008150 | biological_process | No |
| GO:0046483 | heterocycle metabolic process | No |
| GO:0009117 | nucleotide metabolic process | No |
| GO:0034032 | purine nucleoside bisphosphate metabolic process | No |
| GO:0033865 | nucleoside bisphosphate metabolic process | No |
| GO:0044237 | cellular metabolic process | No |
| GO:0005575 | cellular_component | No |
| GO:0006725 | cellular aromatic compound metabolic process | No |
| GO:0003674 | molecular_function | No |
| GO:0044281 | small molecule metabolic process | No |
| GO:0006796 | phosphate-containing compound metabolic process | No |
| GO:0110165 | cellular anatomical entity | No |
| GO:0055086 | nucleobase-containing small molecule metabolic process | No |
| GO:1901564 | organonitrogen compound metabolic process | No |
| GO:0044238 | primary metabolic process | No |
| GO:0009150 | purine ribonucleotide metabolic process | No |
| GO:0006807 | nitrogen compound metabolic process | No |
| GO:0016491 | oxidoreductase activity | No |
| GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | No |
| GO:0006163 | purine nucleotide metabolic process | No |
| GO:0072521 | purine-containing compound metabolic process | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 44 | 0.5 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 237 | 259 | 22 |
| 2 | 266 | 288 | 22 |
| 3 | 292 | 314 | 22 |
| 4 | 371 | 390 | 19 |
| 5 | 395 | 417 | 22 |
| 6 | 482 | 504 | 22 |
| Type of sequence | Sequence |
|---|---|
| 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|10166 MISTSLLPTRFRGEPDRAQQPSAPSRVGKKIAPLLQLLSRVACQHPIQTVVVVALLASTSYVGLLQESLFDRSTA VGKADWSSLVDGSRDLLAGPDTAWKWHSVEHGAADVDHVALLTLVFPDTLSTDSPSSAPPSHAVPTPRNLSITPL PSTENPLTAYSQDSILAYSLPYKEAPEFVSAIQEIPNEGAEETVTRHGRERKTWIMKAAKVDTRSTLAQWLSNAW SEFLDLLKNAETLDIVIMILGYLSMHLTFVSLFLSMRRMGSNFWLATSTLFSSVFAFLFGLAVTAHIGVPVSFIL LSEGLPFLVVTIGFEKNIVLTRAVLSHAVEHRRTQAQASPKSTHESPPQNVIQYAIQAAIKDKGYEILRDYAVEI VILVLGAASGVQGGLQQFCFLAAWILLFDCILLFTFYTAILSIKLEINRIKRHVEMRMALEADGVSRRVAENVAT GEDWLRTGGKGSDDISLFGPKMKSSSVPKFKVLMISGFILINVINICTIPFRSATSLSTLRSWAGGLGGVVSSLP VDPFKVASNGLDAILMAAKASGKPTLVTILTPIKYELEYPSVHYALSSPACDGTADLCPEMSQLDSYGVGGRMVG SLLKSLEDPILSKWIVVALALSVGLNGYLFNVARWGIKDPNVPDRNIDRKELARAQRFNETESATLPLGEYVPPT PQRQDSVTATDDEVDALSLAKLKPTSSSSSVAAAAAEHRSLEELDRMLAEKRAHDMTDEEVVSMSMRGKIPGYAL EKTLKDFTRAVKVRRMIISRTKATAGLTNGLARSKLPYQSYNWERVFGACCENVVGYLPLPVGVAGPLVIDGQSY FIPMATTEGVLVASTSRGCKAINSGGGAITVLTADGMTRGPCVSFETLERAGAAKIWLDSEAGQSVMKKAFNSTS RFARLQTMKTAMAGTNLYIRFKTTTGDAMGMNMISKGVEHALSVMATEGGFEDMSIVSLSGNFCIDKKPAAINWI DGRGKSVVAEAIIPAEVVKGVLKSDVDSLVELNVSKNLIGSAMAGSIGGFNAHAANIVAAIFLATGQDPAQVVES CNCITTMKNLHGSLQISVSMPSLEVGTLGGGTILEPQSAMLDLLGVRGSHPTNPGDNARRLARIIAAGVLAGELS LCSALAAGHLVKAHMQHNRSAATSRAGTPAPAPMTPVSLAMTSAQEKSSTQQPLSAAAQQRSKR* |
| Coding | >Hirsu2|10166 ATGATATCCACTTCCTTGCTTCCAACCCGCTTCCGCGGCGAGCCCGACCGCGCTCAGCAGCCCTCGGCGCCGTCG CGCGTGGGCAAGAAGATAGCGCCTCTGCTCCAGCTCCTGTCCAGGGTGGCGTGCCAGCATCCCATCCAGACCGTC GTCGTCGTCGCCCTCCTCGCCAGCACCTCATACGTCGGCCTCCTCCAAGAAAGCCTCTTCGACCGCTCCACGGCG GTCGGCAAGGCCGACTGGTCCTCGCTCGTCGACGGCAGCCGGGACTTGCTCGCCGGCCCCGACACGGCGTGGAAG TGGCATAGCGTGGAGCACGGCGCCGCCGACGTCGACCATGTCGCCCTGCTGACGCTCGTCTTCCCCGACACCCTC TCCACCGACTCGCCCAGCAGCGCGCCGCCCTCCCACGCCGTCCCGACCCCGCGCAACCTCTCCATCACGCCCCTC CCGTCCACCGAGAACCCCCTGACCGCCTACTCCCAGGACAGCATCCTCGCCTACTCGCTGCCCTACAAGGAGGCC CCCGAGTTCGTCTCCGCCATCCAGGAGATCCCCAACGAGGGCGCCGAGGAGACGGTCACGCGCCACGGCCGCGAG AGGAAGACGTGGATCATGAAGGCCGCCAAGGTCGACACCCGGAGCACCCTGGCCCAGTGGCTCAGCAATGCCTGG TCCGAGTTCCTCGACCTGCTCAAGAACGCCGAGACGCTCGACATCGTCATCATGATCCTCGGCTACCTCTCCATG CACCTGACCTTCGTCTCCCTCTTCCTCTCCATGCGTCGCATGGGCTCCAACTTCTGGCTCGCCACCAGCACCCTC TTCTCCTCCGTCTTCGCCTTCCTCTTCGGCCTCGCCGTCACCGCCCACATCGGCGTGCCCGTCAGCTTCATCCTC CTGTCCGAGGGCCTGCCCTTCCTCGTCGTCACCATCGGCTTCGAAAAGAACATCGTCCTCACTCGCGCCGTTCTC TCGCACGCCGTCGAGCACCGTCGCACCCAGGCCCAGGCCTCGCCCAAGTCGACCCACGAGTCGCCACCGCAAAAC GTCATCCAGTATGCCATACAGGCTGCCATCAAGGACAAGGGCTACGAGATCCTCCGCGACTACGCTGTCGAGATT GTCATCCTCGTCCTTGGGGCGGCCTCCGGGGTCCAGGGCGGGCTTCAGCAATTCTGCTTCCTGGCCGCCTGGATC CTCCTCTTCGACTGCATCCTGCTCTTCACCTTCTACACCGCCATCCTCAGCATCAAGCTCGAGATCAACCGCATC AAGCGCCACGTCGAGATGCGCATGGCGCTCGAGGCCGACGGCGTCAGTCGCCGAGTCGCCGAGAACGTGGCCACG GGCGAAGACTGGTTGCGGACCGGCGGCAAGGGCTCCGACGACATCTCCCTCTTCGGCCCCAAGATGAAGAGCAGC AGCGTGCCCAAGTTCAAGGTGCTCATGATCTCGGGCTTCATCCTCATCAACGTCATCAACATCTGCACCATCCCC TTCCGCAGTGCCACCTCCCTGTCGACCCTCCGCTCCTGGGCCGGCGGCCTCGGCGGCGTAGTGTCCAGCCTGCCC GTCGACCCCTTCAAGGTCGCGTCCAACGGCCTCGACGCCATCCTGATGGCGGCCAAGGCCAGCGGCAAGCCGACC CTGGTGACCATCCTCACTCCCATCAAGTACGAGCTCGAGTACCCCTCGGTCCACTACGCCCTATCGTCCCCGGCC TGTGACGGCACCGCGGACTTGTGCCCTGAGATGAGCCAGCTGGACAGCTACGGCGTCGGCGGCCGCATGGTCGGA AGCCTGCTCAAGAGCCTTGAGGACCCCATCCTGTCCAAGTGGATCGTGGTGGCCCTGGCGTTGAGCGTCGGCCTC AACGGCTATCTCTTCAATGTCGCCCGGTGGGGCATTAAGGACCCAAACGTGCCCGACCGCAACATCGACCGTAAG GAGCTGGCGCGCGCCCAGAGATTCAACGAGACCGAGTCGGCGACCTTGCCTCTGGGTGAATACGTGCCTCCCACG CCGCAGCGTCAGGATTCGGTGACGGCAACAGACGACGAGGTGGACGCGCTCTCGCTGGCCAAGCTCAAGCCAACA AGCAGCTCATCGTCGGTGGCGGCGGCGGCGGCGGAGCATCGGTCGCTGGAGGAGCTGGACAGGATGCTCGCGGAG AAGCGTGCGCACGACATGACAGACGAGGAGGTGGTGTCTATGTCGATGCGCGGCAAGATCCCCGGCTATGCGCTC GAGAAGACGCTGAAGGACTTCACGCGCGCCGTCAAGGTCAGGCGCATGATCATCTCGCGGACCAAGGCAACCGCC GGGCTGACCAACGGCCTGGCCCGGTCGAAGCTCCCATACCAGAGCTACAACTGGGAGCGTGTCTTCGGGGCGTGC TGCGAGAACGTGGTGGGCTACCTGCCGCTGCCCGTGGGCGTGGCTGGCCCCCTCGTCATCGACGGCCAGAGCTAC TTCATCCCGATGGCGACGACGGAGGGCGTGCTGGTGGCGAGCACGAGCAGGGGCTGCAAGGCCATCAACTCGGGC GGGGGCGCCATCACGGTGCTGACGGCGGACGGCATGACGCGCGGCCCGTGCGTCAGCTTCGAGACGCTGGAGCGG GCGGGCGCCGCCAAGATCTGGCTCGACTCGGAGGCGGGCCAGTCGGTGATGAAGAAGGCGTTCAACTCGACCAGC CGGTTCGCACGGCTGCAGACGATGAAGACGGCCATGGCCGGCACCAACCTGTACATCCGGTTCAAGACGACGACG GGCGACGCCATGGGCATGAACATGATCTCCAAGGGCGTCGAGCACGCGCTCAGCGTGATGGCGACGGAGGGCGGC TTTGAAGACATGTCGATCGTGTCGCTGTCAGGCAACTTCTGCATCGACAAGAAGCCGGCGGCCATCAACTGGATC GACGGCCGGGGCAAGAGCGTGGTGGCCGAGGCTATCATCCCGGCCGAGGTGGTCAAGGGCGTGCTCAAGAGCGAC GTCGACTCGCTGGTGGAGCTCAACGTGTCCAAGAACCTGATCGGGTCGGCCATGGCCGGGTCGATCGGCGGCTTC AACGCGCACGCGGCCAACATCGTGGCCGCCATTTTCCTGGCCACCGGCCAGGACCCGGCGCAGGTGGTGGAGAGC TGCAACTGCATCACAACGATGAAGAACCTGCACGGATCGCTTCAGATCTCGGTCTCGATGCCCTCGCTCGAAGTG GGCACGCTGGGGGGCGGCACGATCCTGGAGCCGCAGAGCGCGATGCTCGACCTGCTGGGGGTGCGGGGCTCGCAC CCGACGAACCCGGGCGACAACGCAAGGCGTCTGGCGCGCATAATCGCGGCCGGGGTGCTGGCGGGCGAGCTGTCG CTGTGCAGCGCGCTGGCGGCAGGGCACCTGGTGAAGGCGCACATGCAGCACAACCGGAGCGCGGCGACGTCGCGG GCGGGCACGCCGGCGCCGGCGCCGATGACTCCCGTTTCGCTGGCGATGACGAGCGCGCAGGAGAAGTCGTCGACG CAGCAGCCGCTCAGCGCGGCGGCGCAGCAGAGGTCGAAGCGGTGA |
| Transcript | >Hirsu2|10166 ATGATATCCACTTCCTTGCTTCCAACCCGCTTCCGCGGCGAGCCCGACCGCGCTCAGCAGCCCTCGGCGCCGTCG CGCGTGGGCAAGAAGATAGCGCCTCTGCTCCAGCTCCTGTCCAGGGTGGCGTGCCAGCATCCCATCCAGACCGTC GTCGTCGTCGCCCTCCTCGCCAGCACCTCATACGTCGGCCTCCTCCAAGAAAGCCTCTTCGACCGCTCCACGGCG GTCGGCAAGGCCGACTGGTCCTCGCTCGTCGACGGCAGCCGGGACTTGCTCGCCGGCCCCGACACGGCGTGGAAG TGGCATAGCGTGGAGCACGGCGCCGCCGACGTCGACCATGTCGCCCTGCTGACGCTCGTCTTCCCCGACACCCTC TCCACCGACTCGCCCAGCAGCGCGCCGCCCTCCCACGCCGTCCCGACCCCGCGCAACCTCTCCATCACGCCCCTC CCGTCCACCGAGAACCCCCTGACCGCCTACTCCCAGGACAGCATCCTCGCCTACTCGCTGCCCTACAAGGAGGCC CCCGAGTTCGTCTCCGCCATCCAGGAGATCCCCAACGAGGGCGCCGAGGAGACGGTCACGCGCCACGGCCGCGAG AGGAAGACGTGGATCATGAAGGCCGCCAAGGTCGACACCCGGAGCACCCTGGCCCAGTGGCTCAGCAATGCCTGG TCCGAGTTCCTCGACCTGCTCAAGAACGCCGAGACGCTCGACATCGTCATCATGATCCTCGGCTACCTCTCCATG CACCTGACCTTCGTCTCCCTCTTCCTCTCCATGCGTCGCATGGGCTCCAACTTCTGGCTCGCCACCAGCACCCTC TTCTCCTCCGTCTTCGCCTTCCTCTTCGGCCTCGCCGTCACCGCCCACATCGGCGTGCCCGTCAGCTTCATCCTC CTGTCCGAGGGCCTGCCCTTCCTCGTCGTCACCATCGGCTTCGAAAAGAACATCGTCCTCACTCGCGCCGTTCTC TCGCACGCCGTCGAGCACCGTCGCACCCAGGCCCAGGCCTCGCCCAAGTCGACCCACGAGTCGCCACCGCAAAAC GTCATCCAGTATGCCATACAGGCTGCCATCAAGGACAAGGGCTACGAGATCCTCCGCGACTACGCTGTCGAGATT GTCATCCTCGTCCTTGGGGCGGCCTCCGGGGTCCAGGGCGGGCTTCAGCAATTCTGCTTCCTGGCCGCCTGGATC CTCCTCTTCGACTGCATCCTGCTCTTCACCTTCTACACCGCCATCCTCAGCATCAAGCTCGAGATCAACCGCATC AAGCGCCACGTCGAGATGCGCATGGCGCTCGAGGCCGACGGCGTCAGTCGCCGAGTCGCCGAGAACGTGGCCACG GGCGAAGACTGGTTGCGGACCGGCGGCAAGGGCTCCGACGACATCTCCCTCTTCGGCCCCAAGATGAAGAGCAGC AGCGTGCCCAAGTTCAAGGTGCTCATGATCTCGGGCTTCATCCTCATCAACGTCATCAACATCTGCACCATCCCC TTCCGCAGTGCCACCTCCCTGTCGACCCTCCGCTCCTGGGCCGGCGGCCTCGGCGGCGTAGTGTCCAGCCTGCCC GTCGACCCCTTCAAGGTCGCGTCCAACGGCCTCGACGCCATCCTGATGGCGGCCAAGGCCAGCGGCAAGCCGACC CTGGTGACCATCCTCACTCCCATCAAGTACGAGCTCGAGTACCCCTCGGTCCACTACGCCCTATCGTCCCCGGCC TGTGACGGCACCGCGGACTTGTGCCCTGAGATGAGCCAGCTGGACAGCTACGGCGTCGGCGGCCGCATGGTCGGA AGCCTGCTCAAGAGCCTTGAGGACCCCATCCTGTCCAAGTGGATCGTGGTGGCCCTGGCGTTGAGCGTCGGCCTC AACGGCTATCTCTTCAATGTCGCCCGGTGGGGCATTAAGGACCCAAACGTGCCCGACCGCAACATCGACCGTAAG GAGCTGGCGCGCGCCCAGAGATTCAACGAGACCGAGTCGGCGACCTTGCCTCTGGGTGAATACGTGCCTCCCACG CCGCAGCGTCAGGATTCGGTGACGGCAACAGACGACGAGGTGGACGCGCTCTCGCTGGCCAAGCTCAAGCCAACA AGCAGCTCATCGTCGGTGGCGGCGGCGGCGGCGGAGCATCGGTCGCTGGAGGAGCTGGACAGGATGCTCGCGGAG AAGCGTGCGCACGACATGACAGACGAGGAGGTGGTGTCTATGTCGATGCGCGGCAAGATCCCCGGCTATGCGCTC GAGAAGACGCTGAAGGACTTCACGCGCGCCGTCAAGGTCAGGCGCATGATCATCTCGCGGACCAAGGCAACCGCC GGGCTGACCAACGGCCTGGCCCGGTCGAAGCTCCCATACCAGAGCTACAACTGGGAGCGTGTCTTCGGGGCGTGC TGCGAGAACGTGGTGGGCTACCTGCCGCTGCCCGTGGGCGTGGCTGGCCCCCTCGTCATCGACGGCCAGAGCTAC TTCATCCCGATGGCGACGACGGAGGGCGTGCTGGTGGCGAGCACGAGCAGGGGCTGCAAGGCCATCAACTCGGGC GGGGGCGCCATCACGGTGCTGACGGCGGACGGCATGACGCGCGGCCCGTGCGTCAGCTTCGAGACGCTGGAGCGG GCGGGCGCCGCCAAGATCTGGCTCGACTCGGAGGCGGGCCAGTCGGTGATGAAGAAGGCGTTCAACTCGACCAGC CGGTTCGCACGGCTGCAGACGATGAAGACGGCCATGGCCGGCACCAACCTGTACATCCGGTTCAAGACGACGACG GGCGACGCCATGGGCATGAACATGATCTCCAAGGGCGTCGAGCACGCGCTCAGCGTGATGGCGACGGAGGGCGGC TTTGAAGACATGTCGATCGTGTCGCTGTCAGGCAACTTCTGCATCGACAAGAAGCCGGCGGCCATCAACTGGATC GACGGCCGGGGCAAGAGCGTGGTGGCCGAGGCTATCATCCCGGCCGAGGTGGTCAAGGGCGTGCTCAAGAGCGAC GTCGACTCGCTGGTGGAGCTCAACGTGTCCAAGAACCTGATCGGGTCGGCCATGGCCGGGTCGATCGGCGGCTTC AACGCGCACGCGGCCAACATCGTGGCCGCCATTTTCCTGGCCACCGGCCAGGACCCGGCGCAGGTGGTGGAGAGC TGCAACTGCATCACAACGATGAAGAACCTGCACGGATCGCTTCAGATCTCGGTCTCGATGCCCTCGCTCGAAGTG GGCACGCTGGGGGGCGGCACGATCCTGGAGCCGCAGAGCGCGATGCTCGACCTGCTGGGGGTGCGGGGCTCGCAC CCGACGAACCCGGGCGACAACGCAAGGCGTCTGGCGCGCATAATCGCGGCCGGGGTGCTGGCGGGCGAGCTGTCG CTGTGCAGCGCGCTGGCGGCAGGGCACCTGGTGAAGGCGCACATGCAGCACAACCGGAGCGCGGCGACGTCGCGG GCGGGCACGCCGGCGCCGGCGCCGATGACTCCCGTTTCGCTGGCGATGACGAGCGCGCAGGAGAAGTCGTCGACG CAGCAGCCGCTCAGCGCGGCGGCGCAGCAGAGGTCGAAGCGGTGA |
| Gene | >Hirsu2|10166 ATGATATCCACTTCCTTGCTTCCAACCCGCTTCCGCGGCGAGCCCGACCGCGCTCAGCAGCCCTCGGCGCCGTCG CGCGTGGGCAAGAAGATAGCGCCTCTGCTCCAGCTCCTGTCCAGGGTGGCGTGCCAGCATCCCATCCAGACCGTC GTCGTCGTCGCCCTCCTCGCCAGCACCTCATACGTCGGCCTCCTCCAAGAAAGCCTCTTCGACCGCTCCACGGCG GTCGGCAAGGCCGACTGGTCCTCGCTCGTCGACGGCAGCCGGGACTTGCTCGCCGGCCCCGACACGGCGTGGAAG TGGCATAGCGTGGAGCACGGCGCCGCCGACGTCGACCATGTCGCCCTGCTGACGCTCGTCTTCCCCGACACCCTC TCCACCGACTCGCCCAGCAGCGCGCCGCCCTCCCACGCCGTCCCGACCCCGCGCAACCTCTCCATCACGCCCCTC CCGTCCACCGAGAACCCCCTGACCGCCTACTCCCAGGACAGCATCCTCGCCTACTCGCTGCCCTACAAGGAGGCC CCCGAGTTCGTCTCCGCCATCCAGGAGATCCCCAACGAGGGCGCCGAGGAGACGGTCACGCGCCACGGCCGCGAG AGGAAGACGTGGATCATGAAGGCCGCCAAGGTCGACACCCGGAGCACCCTGGCCCAGTGGCTCAGCAATGCCTGG TCCGAGTTCCTCGACCTGCTCAAGAACGCCGAGACGCTCGACATCGTCATCATGATCCTCGGCTACCTCTCCATG CACCTGACCTTCGTCTCCCTCTTCCTCTCCATGCGTCGCATGGGCTCCAACTTCTGGCTCGCCACCAGCACCCTC TTCTCCTCCGTCTTCGCCTTCCTCTTCGGCCTCGCCGTCACCGCCCACATCGGCGTGCCCGTCAGCTTCATCCTC CTGTCCGAGGGCCTGCCCTTCCTCGTCGTCACCATCGGCTTCGAAAAGAACATCGTCCTCACTCGCGCCGTTCTC TCGCACGCCGTCGAGCACCGTCGCACCCAGGCCCAGGCCTCGCCCAAGTCGACCCACGAGTCGCCACCGCAAAAC GTCATCCAGTATGCCATACAGGCTGCCATCAAGGACAAGGGCTACGAGATCCTCCGCGACTACGCTGTCGAGATT GTCATCCTCGTCCTTGGGGCGGCCTCCGGGGTCCAGGGCGGGCTTCAGCAATTCTGCTTCCTGGCCGCCTGGATC CTCCTCTTCGACTGCATCCTGCTCTTCACCTTCTACACCGCCATCCTCAGCATCAAGCTCGAGATCAACCGCATC AAGCGCCACGTCGAGATGCGCATGGCGCTCGAGGCCGACGGCGTCAGTCGCCGAGTCGCCGAGAACGTGGCCACG GGCGAAGACTGGTTGCGGACCGGCGGCAAGGGCTCCGACGACATCTCCCTCTTCGGCCCCAAGATGAAGAGCAGC AGCGTGCCCAAGTTCAAGGTGCTCATGATCTCGGGCTTCATCCTCATCAACGTCATCAACATCTGCACCATCCCC TTCCGCAGTGCCACCTCCCTGTCGACCCTCCGCTCCTGGGCCGGCGGCCTCGGCGGCGTAGTGTCCAGCCTGCCC GTCGACCCCTTCAAGGTCGCGTCCAACGGCCTCGACGCCATCCTGATGGCGGCCAAGGCCAGCGGCAAGCCGACC CTGGTGACCATCCTCACTCCCATCAAGTACGAGCTCGAGTACCCCTCGGTCCACTACGCCCTATCGTCCCCGGCC TGTGACGGCACCGCGGACTTGTGCCCTGAGATGAGCCAGCTGGACAGCTACGGCGTCGGCGGCCGCATGGTCGGA AGCCTGCTCAAGAGCCTTGAGGACCCCATCCTGTCCAAGTGGATCGTGGTGGCCCTGGCGTTGAGCGTCGGCCTC AACGGCTATCTCTTCAATGTCGCCCGGTGGGGCATTAAGGACCCAAACGTGCCCGACCGCAACATCGACCGTAAG GAGCTGGCGCGCGCCCAGAGATTCAACGAGACCGAGTCGGCGACCTTGCCTCTGGGTGAATACGTGCCTCCCACG CCGCAGCGTCAGGATTCGGTGACGGCAACAGACGACGAGGTGGACGCGCTCTCGCTGGCCAAGCTCAAGCCAACA AGCAGCTCATCGTCGGTGGCGGCGGCGGCGGCGGAGCATCGGTCGCTGGAGGAGCTGGACAGGATGCTCGCGGAG AAGCGTGCGCACGACATGACAGACGAGGAGGTGGTGTCTATGTCGATGCGCGGCAAGATCCCCGGCTATGCGCTC GAGAAGACGCTGAAGGACTTCACGCGCGCCGTCAAGGTCAGGCGCATGATCATCTCGCGGACCAAGGCAACCGCC GGGCTGACCAACGGCCTGGCCCGGTCGAAGCTCCCATACCAGAGCTACAACTGGGAGCGTGTCTTCGGGGCGTGC TGCGAGAACGTGGTGGGCTACCTGCCGCTGCCCGTGGGCGTGGCTGGCCCCCTCGTCATCGACGGCCAGAGCTAC TTCATCCCGATGGCGACGACGGAGGGCGTGCTGGTGGCGAGCACGAGCAGGGGCTGCAAGGCCATCAACTCGGGC GGGGGCGCCATCACGGTGCTGACGGCGGACGGCATGACGCGCGGCCCGTGCGTCAGCTTCGAGACGCTGGAGCGG GCGGGCGCCGCCAAGATCTGGCTCGACTCGGAGGCGGGCCAGTCGGTGATGAAGAAGGCGTTCAACTCGACCAGC CGGTTCGCACGGCTGCAGACGATGAAGACGGCCATGGCCGGCACCAACCTGTACATCCGGTTCAAGACGACGACG GGCGACGCCATGGGCATGAACATGATCTCCAAGGGCGTCGAGCACGCGCTCAGCGTGATGGCGACGGAGGGCGGC TTTGAAGACATGTCGATCGTGTCGCTGTCAGGCAACTTCTGCATCGACAAGAAGCCGGCGGCCATCAACTGGATC GACGGCCGGGGCAAGAGCGTGGTGGCCGAGGCTATCATCCCGGCCGAGGTGGTCAAGGGCGTGCTCAAGAGCGAC GTCGACTCGCTGGTGGAGCTCAACGTGTCCAAGAACCTGATCGGGTCGGCCATGGCCGGGTCGATCGGCGGCTTC AACGCGCACGCGGCCAACATCGTGGCCGCCATTTTCCTGGCCACCGGCCAGGACCCGGCGCAGGTGGTGGAGAGC TGCAACTGCATCACAACGATGAAGAAGTAAGCTCCCCCTTCTTCCCATCATCACTGTCTTTCGACCGTTTCGGAC AACAAGGATTTCCCCCGCCGTCCCCTCCCCCCTGACTCTCGAAGGCTAACCTTTCCCGCCCGCACTGCAGCCTGC ACGGATCGCTTCAGATCTCGGTCTCGATGCCCTCGCTCGAAGTGGGCACGCTGGGGGGCGGCACGATCCTGGAGC CGCAGAGCGCGATGCTCGACCTGCTGGGGGTGCGGGGCTCGCACCCGACGAACCCGGGCGACAACGCAAGGCGTC TGGCGCGCATAATCGCGGCCGGGGTGCTGGCGGGCGAGCTGTCGCTGTGCAGCGCGCTGGCGGCAGGGCACCTGG TGAAGGCGCACATGCAGCACAACCGGAGCGCGGCGACGTCGCGGGCGGGCACGCCGGCGCCGGCGCCGATGACTC CCGTTTCGCTGGCGATGACGAGCGCGCAGGAGAAGTCGTCGACGCAGCAGCCGCTCAGCGCGGCGGCGCAGCAGA GGTCGAAGCGGTGA |