Protein ID | Hirsu2|11007 |
Gene name | |
Location | Contig_944:5833..7523 |
Strand | - |
Gene length (bp) | 1690 |
Transcript length (bp) | 1623 |
Coding sequence length (bp) | 1623 |
Protein length (aa) | 541 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00251 | Glyco_hydro_32N | Glycosyl hydrolases family 32 N-terminal domain | 1.7E-83 | 43 | 355 |
PF08244 | Glyco_hydro_32C | Glycosyl hydrolases family 32 C terminal | 2.9E-06 | 425 | 503 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P10596|INV4_YEASX | Invertase 4 OS=Saccharomyces cerevisiae GN=SUC4 PE=3 SV=1 | 8 | 491 | 3.0E-103 |
sp|P00724|INV2_YEAST | Invertase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SUC2 PE=1 SV=1 | 39 | 491 | 6.0E-103 |
sp|P28999|INU1_KLUMA | Inulinase OS=Kluyveromyces marxianus GN=INU1 PE=1 SV=1 | 3 | 491 | 2.0E-102 |
sp|P10594|INV1_YEASX | Invertase 1 OS=Saccharomyces cerevisiae GN=SUC1 PE=1 SV=1 | 39 | 491 | 6.0E-101 |
sp|A5DHM6|INUE_PICGU | Extracellular exo-inulinase OS=Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN=PGUG_02777 PE=1 SV=2 | 39 | 491 | 9.0E-100 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P10596|INV4_YEASX | Invertase 4 OS=Saccharomyces cerevisiae GN=SUC4 PE=3 SV=1 | 8 | 491 | 3.0E-103 |
sp|P00724|INV2_YEAST | Invertase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SUC2 PE=1 SV=1 | 39 | 491 | 6.0E-103 |
sp|P28999|INU1_KLUMA | Inulinase OS=Kluyveromyces marxianus GN=INU1 PE=1 SV=1 | 3 | 491 | 2.0E-102 |
sp|P10594|INV1_YEASX | Invertase 1 OS=Saccharomyces cerevisiae GN=SUC1 PE=1 SV=1 | 39 | 491 | 6.0E-101 |
sp|A5DHM6|INUE_PICGU | Extracellular exo-inulinase OS=Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN=PGUG_02777 PE=1 SV=2 | 39 | 491 | 9.0E-100 |
sp|P40912|INV1_WICAO | Invertase OS=Wickerhamomyces anomalus GN=INV1 PE=3 SV=1 | 32 | 494 | 1.0E-99 |
sp|Q6BJW6|INV_DEBHA | Invertase OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=INV PE=3 SV=2 | 1 | 494 | 3.0E-99 |
sp|A8W7I5|INUE_PICGM | Extracellular exo-inulinase inuE OS=Meyerozyma guilliermondii PE=1 SV=3 | 39 | 491 | 8.0E-99 |
sp|O42878|INVX_SCHPO | Putative invertase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC8E11.01c PE=3 SV=3 | 37 | 496 | 4.0E-90 |
sp|O59852|INV1_SCHPO | Invertase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=inv1 PE=1 SV=1 | 26 | 525 | 9.0E-90 |
sp|P24133|INV_SCHOC | Invertase OS=Schwanniomyces occidentalis GN=INV PE=1 SV=1 | 1 | 521 | 2.0E-84 |
sp|P05656|SACC_BACSU | Levanase OS=Bacillus subtilis (strain 168) GN=sacC PE=1 SV=1 | 7 | 363 | 2.0E-76 |
sp|Q9Y746|INV_KLULA | Invertase OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=INV1 PE=3 SV=1 | 9 | 491 | 9.0E-75 |
sp|A2R0E0|INUE_ASPNC | Extracellular exo-inulinase inuE OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=inuE PE=2 SV=1 | 20 | 524 | 4.0E-70 |
sp|Q76HP6|INUE_ASPNG | Extracellular exo-inulinase inuE OS=Aspergillus niger GN=inuE PE=1 SV=1 | 20 | 524 | 2.0E-69 |
sp|E1ABX2|INUE_ASPFI | Extracellular exo-inulinase inuE OS=Aspergillus ficuum GN=exoI PE=1 SV=1 | 20 | 524 | 2.0E-69 |
sp|Q96TU3|INUE_ASPAW | Extracellular exo-inulinase inuE OS=Aspergillus awamori GN=inuE PE=1 SV=1 | 14 | 354 | 1.0E-65 |
sp|O31411|SACC_BACL7 | Levanase (Fragment) OS=Bacillus sp. (strain L7) PE=1 SV=2 | 34 | 523 | 6.0E-46 |
sp|O07003|LEVB_BACSU | Levanbiose-producing levanase OS=Bacillus subtilis (strain 168) GN=levB PE=1 SV=1 | 38 | 482 | 1.0E-44 |
sp|O94220|INU2_ASPFI | Extracellular endo-inulinase inu2 OS=Aspergillus ficuum GN=inu2 PE=1 SV=1 | 29 | 343 | 3.0E-43 |
sp|O74641|INUA_ASPNG | Extracellular endo-inulinase inuA OS=Aspergillus niger GN=inuA PE=1 SV=1 | 29 | 343 | 3.0E-43 |
sp|O74642|INUB_ASPNG | Extracellular endo-inulinase inuB OS=Aspergillus niger GN=inuB PE=1 SV=1 | 29 | 422 | 1.0E-42 |
sp|A5ABL2|INUA_ASPNC | Extracellular endo-inulinase inuA OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=inuA PE=1 SV=1 | 29 | 343 | 4.0E-42 |
sp|P94469|LEVB_GEOSE | Levanbiose-producing levanase (Fragment) OS=Geobacillus stearothermophilus GN=levB PE=1 SV=2 | 62 | 355 | 4.0E-41 |
sp|O33833|BFRA_THEMA | Beta-fructosidase OS=Thermotoga maritima (strain ATCC 43589 / MSB8 / DSM 3109 / JCM 10099) GN=bfrA PE=1 SV=1 | 38 | 341 | 1.0E-38 |
sp|P49174|INVA_MAIZE | Beta-fructofuranosidase, cell wall isozyme OS=Zea mays PE=2 SV=1 | 20 | 368 | 5.0E-32 |
sp|Q67XZ3|INV3_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV3 OS=Arabidopsis thaliana GN=CWINV3 PE=1 SV=2 | 8 | 346 | 4.0E-29 |
sp|Q03174|FRUA_STRMU | Fructan beta-fructosidase OS=Streptococcus mutans serotype c (strain ATCC 700610 / UA159) GN=fruA PE=2 SV=2 | 34 | 300 | 4.0E-29 |
sp|Q0JDC6|INV3_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 3 OS=Oryza sativa subsp. japonica GN=CIN3 PE=2 SV=1 | 36 | 342 | 9.0E-28 |
sp|Q01IS8|INV3_ORYSI | Beta-fructofuranosidase, insoluble isoenzyme 3 OS=Oryza sativa subsp. indica GN=CIN3 PE=2 SV=2 | 36 | 342 | 9.0E-28 |
sp|Q43866|INV1_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV1 OS=Arabidopsis thaliana GN=CWINV1 PE=1 SV=1 | 37 | 346 | 1.0E-27 |
sp|P0DJA7|SCR_ZYMMO | Sucrose-6-phosphate hydrolase OS=Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) GN=sacA PE=1 SV=1 | 40 | 370 | 3.0E-27 |
sp|P16553|RAFD_ECOLX | Raffinose invertase OS=Escherichia coli GN=rafD PE=3 SV=1 | 20 | 391 | 1.0E-26 |
sp|F8DVG5|SCR_ZYMMA | Sucrose-6-phosphate hydrolase OS=Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) GN=sacA PE=3 SV=1 | 40 | 370 | 2.0E-26 |
sp|Q9LIB9|INV5_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV5 OS=Arabidopsis thaliana GN=CWINV5 PE=2 SV=2 | 6 | 355 | 3.0E-26 |
sp|Q0JDC5|INV2_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 2 OS=Oryza sativa subsp. japonica GN=CIN2 PE=1 SV=1 | 22 | 381 | 3.0E-26 |
sp|Q01IS7|INV2_ORYSI | Beta-fructofuranosidase, insoluble isoenzyme 2 OS=Oryza sativa subsp. indica GN=CIN2 PE=2 SV=2 | 22 | 381 | 4.0E-26 |
sp|P80065|INVB_DAUCA | Beta-fructofuranosidase, soluble isoenzyme I OS=Daucus carota GN=INV*DC4 PE=1 SV=2 | 39 | 529 | 7.0E-26 |
sp|Q43089|INV1_PEA | Beta-fructofuranosidase, cell wall isozyme OS=Pisum sativum GN=BFRUCT1 PE=2 SV=1 | 37 | 381 | 1.0E-25 |
sp|Q70XE6|6FEH_BETVU | Fructan 6-exohydrolase OS=Beta vulgaris GN=6-FEH PE=1 SV=1 | 37 | 480 | 1.0E-25 |
sp|P40714|CSCA_ECOLX | Sucrose-6-phosphate hydrolase OS=Escherichia coli GN=cscA PE=3 SV=1 | 35 | 355 | 1.0E-24 |
sp|A1STJ9|SCRB_PSYIN | Probable sucrose-6-phosphate hydrolase OS=Psychromonas ingrahamii (strain 37) GN=Ping_0974 PE=3 SV=1 | 11 | 230 | 2.0E-24 |
sp|P26792|INV1_DAUCA | Beta-fructofuranosidase, insoluble isoenzyme 1 OS=Daucus carota GN=INV1 PE=1 SV=1 | 38 | 382 | 5.0E-24 |
sp|Q0E0P0|INV1_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 1 OS=Oryza sativa subsp. japonica GN=CIN1 PE=2 SV=1 | 22 | 368 | 8.0E-24 |
sp|Q39693|INV3_DAUCA | Beta-fructofuranosidase, insoluble isoenzyme 3 OS=Daucus carota GN=INV3 PE=3 SV=1 | 27 | 422 | 2.0E-23 |
sp|A2X5P7|INV1_ORYSI | Beta-fructofuranosidase, insoluble isoenzyme 1 OS=Oryza sativa subsp. indica GN=CIN1 PE=2 SV=2 | 22 | 370 | 3.0E-23 |
sp|P07819|SCRB_BACSU | Sucrose-6-phosphate hydrolase OS=Bacillus subtilis (strain 168) GN=sacA PE=3 SV=2 | 27 | 491 | 5.0E-23 |
sp|Q5JJV0|INV4_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 4 OS=Oryza sativa subsp. japonica GN=CIN4 PE=2 SV=1 | 11 | 341 | 1.0E-22 |
sp|Q39692|INV2_DAUCA | Beta-fructofuranosidase, insoluble isoenzyme 2 OS=Daucus carota GN=INV2 PE=3 SV=1 | 38 | 365 | 5.0E-22 |
sp|P29000|INVA_SOLLC | Acid beta-fructofuranosidase OS=Solanum lycopersicum GN=TIV1 PE=2 SV=1 | 39 | 522 | 6.0E-22 |
sp|Q39041|INVA4_ARATH | Acid beta-fructofuranosidase 4, vacuolar OS=Arabidopsis thaliana GN=BFRUCT4 PE=2 SV=2 | 39 | 357 | 1.0E-21 |
sp|Q1PEF8|INV2_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV2 OS=Arabidopsis thaliana GN=CWINV2 PE=2 SV=1 | 3 | 346 | 6.0E-21 |
sp|Q43348|INVA3_ARATH | Acid beta-fructofuranosidase 3, vacuolar OS=Arabidopsis thaliana GN=BFRUCT3 PE=2 SV=1 | 39 | 341 | 6.0E-21 |
sp|Q84LA1|1FEH2_WHEAT | Fructan 1-exohydrolase w2 OS=Triticum aestivum GN=1-FEHw2 PE=1 SV=1 | 38 | 341 | 1.0E-20 |
sp|B6DZD2|1FEH_AEGTA | Fructan 1-exohydrolase OS=Aegilops tauschii GN=1-FEH PE=3 SV=1 | 38 | 341 | 1.0E-20 |
sp|P93761|INV1_CAPAN | Acid beta-fructofuranosidase AIV-18 OS=Capsicum annuum PE=2 SV=1 | 39 | 355 | 2.0E-20 |
sp|B6DZD0|1FEH_TRIUA | Fructan 1-exohydrolase OS=Triticum urartu GN=1-FEH PE=3 SV=1 | 38 | 341 | 2.0E-20 |
sp|Q8W413|INV4_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV4 OS=Arabidopsis thaliana GN=CWINV4 PE=2 SV=1 | 38 | 380 | 3.0E-20 |
sp|Q43857|INVA_VICFA | Acid beta-fructofuranosidase OS=Vicia faba GN=VCINV PE=2 SV=1 | 39 | 355 | 4.0E-20 |
sp|B6DZD1|1FEH_AEGSP | Fructan 1-exohydrolase OS=Aegilops speltoides GN=1-FEH PE=3 SV=1 | 16 | 341 | 5.0E-20 |
sp|O24509|INVA_PHAVU | Acid beta-fructofuranosidase OS=Phaseolus vulgaris PE=2 SV=1 | 39 | 355 | 1.0E-19 |
sp|Q2UXF7|6FEH_WHEAT | Fructan 6-exohydrolase OS=Triticum aestivum GN=6-FEH PE=1 SV=1 | 4 | 346 | 1.0E-19 |
sp|B6DZC8|1FEH3_WHEAT | Fructan 1-exohydrolase w3 OS=Triticum aestivum GN=1-FEHw3 PE=1 SV=1 | 18 | 341 | 1.0E-19 |
sp|P49175|INV1_MAIZE | Beta-fructofuranosidase 1 OS=Zea mays GN=IVR1 PE=3 SV=1 | 39 | 491 | 1.0E-19 |
sp|Q84PN8|1FEH1_WHEAT | Fructan 1-exohydrolase w1 OS=Triticum aestivum GN=1-FEHw1 PE=1 SV=1 | 38 | 346 | 2.0E-19 |
sp|P29001|INVA_VIGRR | Acid beta-fructofuranosidase OS=Vigna radiata var. radiata GN=INVA PE=1 SV=1 | 39 | 357 | 3.0E-19 |
sp|P37075|SCRB_SALTM | Sucrose-6-phosphate hydrolase OS=Salmonella typhimurium GN=scrB PE=3 SV=1 | 20 | 234 | 4.0E-19 |
sp|D2IGW7|1FEH_BROPI | Fructan 1-exohydrolase OS=Bromus pictus GN=1-FEHa PE=1 SV=1 | 23 | 341 | 8.0E-19 |
sp|A5EZZ8|SCRB_VIBC3 | Probable sucrose-6-phosphate hydrolase OS=Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) GN=cscA PE=3 SV=1 | 14 | 230 | 1.0E-18 |
sp|B6DXP5|1FEH_LEYCH | Fructan 1-exohydrolase OS=Leymus chinensis GN=1-FEH PE=2 SV=1 | 16 | 357 | 1.0E-18 |
sp|P27217|SCRB_KLEPN | Sucrose-6-phosphate hydrolase OS=Klebsiella pneumoniae GN=scrB PE=1 SV=3 | 20 | 234 | 2.0E-18 |
sp|Q70AT7|1FEH_HORVU | Fructan 1-exohydrolase OS=Hordeum vulgare GN=1-FEH PE=2 SV=1 | 38 | 341 | 4.0E-18 |
sp|Q9FSV7|SST_FESAR | Sucrose:sucrose 1-fructosyltransferase OS=Festuca arundinacea GN=1-SST PE=1 SV=1 | 16 | 347 | 8.0E-18 |
sp|Q9KLT6|SCRB_VIBCH | Probable sucrose-6-phosphate hydrolase OS=Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) GN=VC_A0655 PE=3 SV=1 | 1 | 230 | 2.0E-17 |
sp|Q56UD0|INV6_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 6 OS=Oryza sativa subsp. japonica GN=CIN6 PE=2 SV=1 | 29 | 357 | 3.0E-17 |
sp|Q56660|SCRB_VIBCL | Probable sucrose-6-phosphate hydrolase OS=Vibrio cholerae PE=3 SV=1 | 37 | 230 | 4.0E-17 |
sp|Q5FC15|GFT_ASPOF | 6(G)-fructosyltransferase OS=Asparagus officinalis GN=FT1 PE=1 SV=1 | 39 | 357 | 5.0E-17 |
sp|P13394|SCRB_VIBAL | Sucrose-6-phosphate hydrolase OS=Vibrio alginolyticus GN=scrB PE=2 SV=1 | 40 | 494 | 4.0E-16 |
sp|Q8W4S6|INV6_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV6 OS=Arabidopsis thaliana GN=CWINV6 PE=2 SV=1 | 39 | 357 | 1.0E-14 |
sp|Q05936|SCRB_STAXY | Sucrose-6-phosphate hydrolase OS=Staphylococcus xylosus GN=scrB PE=3 SV=1 | 38 | 504 | 2.0E-12 |
sp|P43471|SCRB_PEDPE | Sucrose-6-phosphate hydrolase OS=Pediococcus pentosaceus GN=scrB PE=3 SV=2 | 38 | 341 | 2.0E-12 |
sp|Q04937|SCRB_LACLL | Sucrose-6-phosphate hydrolase OS=Lactococcus lactis subsp. lactis GN=scrB PE=1 SV=1 | 20 | 389 | 3.0E-12 |
sp|Q56UD1|INV5_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 5 OS=Oryza sativa subsp. japonica GN=CIN5 PE=2 SV=3 | 39 | 357 | 6.0E-12 |
sp|P92916|GFT_ALLCE | Bifunctional 6(G)-fructosyltransferase/2,1-fructan:2,1-fructan 1-fructosyltransferase OS=Allium cepa PE=1 SV=1 | 39 | 380 | 2.0E-11 |
sp|P07635|INV7_YEASX | Invertase 7 (Fragments) OS=Saccharomyces cerevisiae GN=SUC7 PE=3 SV=1 | 8 | 79 | 1.0E-09 |
sp|P10597|INV5_YEASX | Invertase 5 (Fragment) OS=Saccharomyces cerevisiae GN=SUC5 PE=3 SV=1 | 8 | 79 | 1.0E-09 |
sp|P10595|INV3_YEASX | Invertase 3 (Fragment) OS=Saccharomyces cerevisiae GN=SUC3 PE=3 SV=1 | 8 | 79 | 1.0E-09 |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Extracellular|Lysosome/Vacuole | Signal peptide | 0.1891 | 0.0969 | 0.9176 | 0.1226 | 0.0843 | 0.0908 | 0.3794 | 0.7091 | 0.3485 | 0.0375 |
SignalP signal predicted | Location | Score |
---|---|---|
Yes | 1 - 23 | 0.999719 |
CAZyme category | E-value | Start | End |
---|---|---|---|
GH32 | 8.9E-93 | 43 | 355 |
Orthofinder run ID | 4 |
Orthogroup | 4861 |
Change Orthofinder run |
Type of sequence | Sequence |
---|---|
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|11007 MTRFAAVVLLQLLLAGASTAVSASASEGVPPADYGGPYRPQVHFSPPQHFMNDPNGLFRDARGIWHLYYQYNPTG LVAGNQHWGHATSRDLYRWVNQPIALFPPADEVSVFSGSVVVDRNNTSGFFPDQKDGVVAIYTLAGPERQSQAIA YSRDGGYSFTPYPGNPVIPGNSTQFRDPKVIWHGSRWVMVVAYAVDFAVGIFTSRNLIDWTPASNFSHHGLLGLQ WECPNLVPVPYIDDQGARHHDMWLMVVSVNPGGPLGGSVTQYFPGTFDGTHFRAVDRAARILDFGKDNYAGQFFY DVDNEDPVFMAWASNWQYTQTVPTDREGWRGAMSLPRHVYLTKAPKTGWKLVSRPYDLSPVMGGELLSKSGFANA DLRVGFAEIRSNALYWEAHVTGLPGGGLSDKATLNFTFQSGRSGESLGGGFFFAAGSFYLDRGAARGFDDAFFTD KFSVDTAWSGRSSWSMSGVMDRSILEVFVDGGVESATITFFTEEPLTQMVFATSELPPEALVSVRVNALQSAWSI PGSTDDYLGAGVQEA* |
Coding | >Hirsu2|11007 ATGACACGCTTCGCCGCCGTTGTTCTGCTCCAGCTTCTTCTCGCCGGAGCCTCCACGGCGGTGTCGGCATCCGCA TCCGAGGGCGTTCCGCCCGCCGACTACGGCGGCCCGTACCGGCCCCAGGTCCACTTTTCTCCTCCGCAGCACTTC ATGAACGATCCCAACGGCCTGTTCCGCGACGCACGGGGCATTTGGCATCTCTACTACCAGTACAACCCTACCGGC CTCGTTGCCGGCAACCAGCACTGGGGACACGCCACCTCGCGGGACCTGTATCGCTGGGTCAACCAGCCGATCGCC CTGTTCCCCCCGGCCGATGAGGTCTCCGTCTTCTCCGGGAGCGTCGTCGTGGATCGCAACAACACGTCGGGCTTC TTCCCGGACCAGAAAGACGGCGTCGTGGCCATCTACACTCTGGCCGGCCCCGAGCGTCAGTCGCAGGCAATCGCC TATTCCCGCGATGGCGGCTACAGCTTCACGCCATACCCCGGGAACCCCGTCATCCCGGGCAACTCAACCCAGTTC CGCGACCCAAAAGTCATCTGGCACGGGAGCCGCTGGGTCATGGTCGTAGCCTACGCCGTCGACTTCGCCGTCGGC ATCTTCACCTCTCGCAACCTCATTGACTGGACCCCTGCCAGCAACTTCTCCCACCACGGGCTCCTCGGCCTGCAG TGGGAATGCCCCAACCTGGTGCCCGTTCCGTACATCGACGACCAGGGCGCCAGGCACCACGACATGTGGCTCATG GTCGTCTCCGTCAACCCCGGCGGTCCGCTTGGGGGCTCCGTGACCCAGTACTTCCCTGGTACGTTTGATGGGACT CATTTCCGGGCCGTTGACCGGGCCGCGCGCATCCTCGACTTTGGCAAGGACAACTACGCGGGGCAGTTCTTCTAT GACGTTGACAACGAAGATCCCGTTTTCATGGCCTGGGCCTCCAACTGGCAGTACACACAGACCGTCCCGACCGAT CGCGAAGGTTGGAGGGGGGCCATGAGCCTCCCTCGCCACGTGTATCTGACTAAAGCCCCCAAGACGGGCTGGAAG CTCGTCTCTCGTCCCTACGACCTCAGTCCGGTCATGGGAGGAGAGCTCTTGTCCAAGAGCGGTTTTGCAAACGCT GACTTGAGGGTCGGCTTTGCCGAGATACGCTCCAACGCCCTGTATTGGGAAGCACACGTGACGGGCTTGCCCGGA GGTGGCCTGTCGGATAAAGCCACACTGAATTTCACCTTCCAGAGTGGTCGTTCGGGCGAAAGCCTTGGGGGAGGA TTCTTCTTCGCCGCAGGCTCCTTCTACCTTGACCGCGGTGCTGCGCGAGGCTTCGATGACGCTTTCTTTACAGAC AAGTTCTCCGTCGACACAGCGTGGTCGGGAAGAAGCTCGTGGAGCATGAGCGGTGTCATGGATCGGTCCATTCTC GAAGTTTTTGTGGACGGAGGCGTCGAAAGCGCCACGATAACTTTCTTCACCGAGGAGCCGTTGACTCAAATGGTG TTTGCCACCTCGGAACTCCCCCCGGAGGCCCTTGTTAGTGTTCGCGTGAATGCCCTGCAGAGCGCTTGGAGCATC CCGGGGAGCACGGACGATTACTTGGGTGCCGGAGTGCAGGAGGCGTAG |
Transcript | >Hirsu2|11007 ATGACACGCTTCGCCGCCGTTGTTCTGCTCCAGCTTCTTCTCGCCGGAGCCTCCACGGCGGTGTCGGCATCCGCA TCCGAGGGCGTTCCGCCCGCCGACTACGGCGGCCCGTACCGGCCCCAGGTCCACTTTTCTCCTCCGCAGCACTTC ATGAACGATCCCAACGGCCTGTTCCGCGACGCACGGGGCATTTGGCATCTCTACTACCAGTACAACCCTACCGGC CTCGTTGCCGGCAACCAGCACTGGGGACACGCCACCTCGCGGGACCTGTATCGCTGGGTCAACCAGCCGATCGCC CTGTTCCCCCCGGCCGATGAGGTCTCCGTCTTCTCCGGGAGCGTCGTCGTGGATCGCAACAACACGTCGGGCTTC TTCCCGGACCAGAAAGACGGCGTCGTGGCCATCTACACTCTGGCCGGCCCCGAGCGTCAGTCGCAGGCAATCGCC TATTCCCGCGATGGCGGCTACAGCTTCACGCCATACCCCGGGAACCCCGTCATCCCGGGCAACTCAACCCAGTTC CGCGACCCAAAAGTCATCTGGCACGGGAGCCGCTGGGTCATGGTCGTAGCCTACGCCGTCGACTTCGCCGTCGGC ATCTTCACCTCTCGCAACCTCATTGACTGGACCCCTGCCAGCAACTTCTCCCACCACGGGCTCCTCGGCCTGCAG TGGGAATGCCCCAACCTGGTGCCCGTTCCGTACATCGACGACCAGGGCGCCAGGCACCACGACATGTGGCTCATG GTCGTCTCCGTCAACCCCGGCGGTCCGCTTGGGGGCTCCGTGACCCAGTACTTCCCTGGTACGTTTGATGGGACT CATTTCCGGGCCGTTGACCGGGCCGCGCGCATCCTCGACTTTGGCAAGGACAACTACGCGGGGCAGTTCTTCTAT GACGTTGACAACGAAGATCCCGTTTTCATGGCCTGGGCCTCCAACTGGCAGTACACACAGACCGTCCCGACCGAT CGCGAAGGTTGGAGGGGGGCCATGAGCCTCCCTCGCCACGTGTATCTGACTAAAGCCCCCAAGACGGGCTGGAAG CTCGTCTCTCGTCCCTACGACCTCAGTCCGGTCATGGGAGGAGAGCTCTTGTCCAAGAGCGGTTTTGCAAACGCT GACTTGAGGGTCGGCTTTGCCGAGATACGCTCCAACGCCCTGTATTGGGAAGCACACGTGACGGGCTTGCCCGGA GGTGGCCTGTCGGATAAAGCCACACTGAATTTCACCTTCCAGAGTGGTCGTTCGGGCGAAAGCCTTGGGGGAGGA TTCTTCTTCGCCGCAGGCTCCTTCTACCTTGACCGCGGTGCTGCGCGAGGCTTCGATGACGCTTTCTTTACAGAC AAGTTCTCCGTCGACACAGCGTGGTCGGGAAGAAGCTCGTGGAGCATGAGCGGTGTCATGGATCGGTCCATTCTC GAAGTTTTTGTGGACGGAGGCGTCGAAAGCGCCACGATAACTTTCTTCACCGAGGAGCCGTTGACTCAAATGGTG TTTGCCACCTCGGAACTCCCCCCGGAGGCCCTTGTTAGTGTTCGCGTGAATGCCCTGCAGAGCGCTTGGAGCATC CCGGGGAGCACGGACGATTACTTGGGTGCCGGAGTGCAGGAGGCGTAG |
Gene | >Hirsu2|11007 ATGACACGCTTCGCCGCCGTTGTTCTGCTCCAGCTTCTTCTCGCCGGAGCCTCCACGGCGGTGTCGGCATCCGCA TCCGAGGGCGTTCCGCCCGCCGACTACGGCGGCCCGTACCGGCCCCAGGTCCACTTTTCTCCTCCGCAGCACTTC ATGAACGATCCCAACGGCCTGTTCCGCGACGCACGGGGCATTTGGCATCTCTACTACCAGTACAACCCTACCGGC CTCGTTGCCGGCAACCAGCACTGGGGACACGCCACCTCGCGGGACCTGTATCGCTGGGTCAACCAGCCGATCGCC CTGTTCCCCCCGGCCGATGAGGTCTCCGTCTTCTCCGGGAGCGTCGTCGTGGATCGCAACAACACGTCGGGCTTC TTCCCGGACCAGAAAGACGGCGTCGTGGCCATCTACGTGAGTCGGCGGCGACCAGCGCACGAGGATCGTCGTCGT CGGCCTTGCTCACCATGGGTTATGATAGACTCTGGCCGGCCCCGAGCGTCAGTCGCAGGCAATCGCCTATTCCCG CGATGGCGGCTACAGCTTCACGCCATACCCCGGGAACCCCGTCATCCCGGGCAACTCAACCCAGTTCCGCGACCC AAAAGTCATCTGGCACGGGAGCCGCTGGGTCATGGTCGTAGCCTACGCCGTCGACTTCGCCGTCGGCATCTTCAC CTCTCGCAACCTCATTGACTGGACCCCTGCCAGCAACTTCTCCCACCACGGGCTCCTCGGCCTGCAGTGGGAATG CCCCAACCTGGTGCCCGTTCCGTACATCGACGACCAGGGCGCCAGGCACCACGACATGTGGCTCATGGTCGTCTC CGTCAACCCCGGCGGTCCGCTTGGGGGCTCCGTGACCCAGTACTTCCCTGGTACGTTTGATGGGACTCATTTCCG GGCCGTTGACCGGGCCGCGCGCATCCTCGACTTTGGCAAGGACAACTACGCGGGGCAGTTCTTCTATGACGTTGA CAACGAAGATCCCGTTTTCATGGCCTGGGCCTCCAACTGGCAGTACACACAGACCGTCCCGACCGATCGCGAAGG TTGGAGGGGGGCCATGAGCCTCCCTCGCCACGTGTATCTGACTAAAGCCCCCAAGACGGGCTGGAAGCTCGTCTC TCGTCCCTACGACCTCAGTCCGGTCATGGGAGGAGAGCTCTTGTCCAAGAGCGGTTTTGCAAACGCTGACTTGAG GGTCGGCTTTGCCGAGATACGCTCCAACGCCCTGTATTGGGAAGCACACGTGACGGGCTTGCCCGGAGGTGGCCT GTCGGATAAAGCCACACTGAATTTCACCTTCCAGAGTGGTCGTTCGGGCGAAAGCCTTGGGGGAGGATTCTTCTT CGCCGCAGGCTCCTTCTACCTTGACCGCGGTGCTGCGCGAGGCTTCGATGACGCTTTCTTTACAGACAAGTTCTC CGTCGACACAGCGTGGTCGGGAAGAAGCTCGTGGAGCATGAGCGGTGTCATGGATCGGTCCATTCTCGAAGTTTT TGTGGACGGAGGCGTCGAAAGCGCCACGATAACTTTCTTCACCGAGGAGCCGTTGACTCAAATGGTGTTTGCCAC CTCGGAACTCCCCCCGGAGGCCCTTGTTAGTGTTCGCGTGAATGCCCTGCAGAGCGCTTGGAGCATCCCGGGGAG CACGGACGATTACTTGGGTGCCGGAGTGCAGGAGGCGTAG |