Protein ID | Hirsu2|10848 |
Gene name | |
Location | Contig_913:6600..8467 |
Strand | + |
Gene length (bp) | 1867 |
Transcript length (bp) | 1551 |
Coding sequence length (bp) | 1551 |
Protein length (aa) | 517 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00282 | Pyridoxal_deC | Pyridoxal-dependent decarboxylase conserved domain | 2.7E-72 | 66 | 391 |
PF00266 | Aminotran_5 | Aminotransferase class-V | 1.9E-12 | 110 | 394 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q42472|DCE2_ARATH | Glutamate decarboxylase 2 OS=Arabidopsis thaliana GN=GAD2 PE=1 SV=1 | 28 | 479 | 2.0E-163 |
sp|Q07346|DCE_PETHY | Glutamate decarboxylase OS=Petunia hybrida GN=GAD PE=1 SV=1 | 34 | 464 | 4.0E-163 |
sp|P54767|DCE_SOLLC | Glutamate decarboxylase OS=Solanum lycopersicum PE=2 SV=1 | 29 | 483 | 3.0E-162 |
sp|Q9ZPS3|DCE4_ARATH | Glutamate decarboxylase 4 OS=Arabidopsis thaliana GN=GAD4 PE=1 SV=1 | 34 | 516 | 2.0E-161 |
sp|Q42521|DCE1_ARATH | Glutamate decarboxylase 1 OS=Arabidopsis thaliana GN=GAD1 PE=1 SV=2 | 34 | 474 | 4.0E-161 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q42472|DCE2_ARATH | Glutamate decarboxylase 2 OS=Arabidopsis thaliana GN=GAD2 PE=1 SV=1 | 28 | 479 | 2.0E-163 |
sp|Q07346|DCE_PETHY | Glutamate decarboxylase OS=Petunia hybrida GN=GAD PE=1 SV=1 | 34 | 464 | 4.0E-163 |
sp|P54767|DCE_SOLLC | Glutamate decarboxylase OS=Solanum lycopersicum PE=2 SV=1 | 29 | 483 | 3.0E-162 |
sp|Q9ZPS3|DCE4_ARATH | Glutamate decarboxylase 4 OS=Arabidopsis thaliana GN=GAD4 PE=1 SV=1 | 34 | 516 | 2.0E-161 |
sp|Q42521|DCE1_ARATH | Glutamate decarboxylase 1 OS=Arabidopsis thaliana GN=GAD1 PE=1 SV=2 | 34 | 474 | 4.0E-161 |
sp|Q9LSH2|DCE5_ARATH | Glutamate decarboxylase 5 OS=Arabidopsis thaliana GN=GAD5 PE=2 SV=1 | 29 | 464 | 3.0E-158 |
sp|Q9ZPS4|DCE3_ARATH | Glutamate decarboxylase 3 OS=Arabidopsis thaliana GN=GAD3 PE=2 SV=1 | 27 | 480 | 5.0E-151 |
sp|Q928R9|DCEB_LISIN | Glutamate decarboxylase beta OS=Listeria innocua serovar 6a (strain CLIP 11262) GN=gadB PE=3 SV=1 | 24 | 480 | 1.0E-127 |
sp|Q9EYW9|DCEB_LISMO | Glutamate decarboxylase beta OS=Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) GN=gadB PE=3 SV=2 | 24 | 480 | 2.0E-127 |
sp|O30418|DCE_LACLM | Glutamate decarboxylase OS=Lactococcus lactis subsp. cremoris (strain MG1363) GN=gadB PE=1 SV=2 | 30 | 465 | 2.0E-123 |
sp|Q9CG20|DCE_LACLA | Glutamate decarboxylase OS=Lactococcus lactis subsp. lactis (strain IL1403) GN=gadB PE=1 SV=1 | 30 | 465 | 4.0E-122 |
sp|Q8Y4K4|DCEC_LISMO | Probable glutamate decarboxylase gamma OS=Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) GN=lmo2434 PE=3 SV=1 | 25 | 464 | 6.0E-121 |
sp|P58228|DCEA_ECO57 | Glutamate decarboxylase alpha OS=Escherichia coli O157:H7 GN=gadA PE=3 SV=1 | 30 | 463 | 3.0E-120 |
sp|P69908|DCEA_ECOLI | Glutamate decarboxylase alpha OS=Escherichia coli (strain K12) GN=gadA PE=1 SV=1 | 30 | 463 | 8.0E-120 |
sp|P69909|DCEA_ECOL6 | Glutamate decarboxylase alpha OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=gadA PE=1 SV=1 | 30 | 463 | 8.0E-120 |
sp|P69912|DCEB_SHIFL | Glutamate decarboxylase beta OS=Shigella flexneri GN=gadB PE=3 SV=1 | 30 | 463 | 9.0E-120 |
sp|P69910|DCEB_ECOLI | Glutamate decarboxylase beta OS=Escherichia coli (strain K12) GN=gadB PE=1 SV=1 | 30 | 463 | 9.0E-120 |
sp|P69911|DCEB_ECO57 | Glutamate decarboxylase beta OS=Escherichia coli O157:H7 GN=gadB PE=3 SV=1 | 30 | 463 | 9.0E-120 |
sp|Q83PR1|DCEA_SHIFL | Glutamate decarboxylase alpha OS=Shigella flexneri GN=gadA PE=3 SV=2 | 30 | 463 | 2.0E-119 |
sp|Q928K4|DCEC_LISIN | Probable glutamate decarboxylase gamma OS=Listeria innocua serovar 6a (strain CLIP 11262) GN=lin2528 PE=3 SV=1 | 25 | 464 | 2.0E-119 |
sp|Q8FHG5|DCEB_ECOL6 | Glutamate decarboxylase beta OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=gadB PE=3 SV=2 | 30 | 463 | 5.0E-119 |
sp|Q54VQ5|GADA_DICDI | Glutamate decarboxylase A OS=Dictyostelium discoideum GN=gadA PE=2 SV=1 | 36 | 480 | 2.0E-117 |
sp|Q54IJ3|GADB_DICDI | Glutamate decarboxylase B OS=Dictyostelium discoideum GN=gadB PE=2 SV=1 | 41 | 465 | 3.0E-114 |
sp|Q9F5P3|DCEA_LISMO | Glutamate decarboxylase alpha OS=Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) GN=gadA PE=3 SV=2 | 29 | 463 | 1.0E-109 |
sp|Q04792|DCE_YEAST | Glutamate decarboxylase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GAD1 PE=1 SV=1 | 41 | 473 | 7.0E-100 |
sp|Q8TV92|MFNA_METKA | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanopyrus kandleri (strain AV19 / DSM 6324 / JCM 9639 / NBRC 100938) GN=mfnA PE=3 SV=1 | 97 | 395 | 3.0E-31 |
sp|Q0W498|MFNA_METAR | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanocella arvoryzae (strain DSM 22066 / NBRC 105507 / MRE50) GN=mfnA PE=3 SV=1 | 95 | 374 | 2.0E-26 |
sp|Q9V7Y2|SGPL_DROME | Sphingosine-1-phosphate lyase OS=Drosophila melanogaster GN=Sply PE=2 SV=1 | 93 | 479 | 5.0E-26 |
sp|Q9UZD5|MFNA_PYRAB | Probable L-aspartate decarboxylase OS=Pyrococcus abyssi (strain GE5 / Orsay) GN=mfnA PE=3 SV=1 | 48 | 372 | 3.0E-25 |
sp|O58679|MFNA_PYRHO | L-aspartate/L-glutamate decarboxylase OS=Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) GN=mfnA PE=1 SV=1 | 98 | 457 | 6.0E-25 |
sp|Q8U1P6|MFNA_PYRFU | Probable L-aspartate decarboxylase OS=Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) GN=mfnA PE=3 SV=1 | 98 | 371 | 1.0E-24 |
sp|A0B9M9|MFNA_METTP | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanosaeta thermophila (strain DSM 6194 / JCM 14653 / NBRC 101360 / PT) GN=mfnA PE=3 SV=2 | 98 | 436 | 1.0E-24 |
sp|C5A2X8|MFNA_THEGJ | Probable L-aspartate decarboxylase OS=Thermococcus gammatolerans (strain DSM 15229 / JCM 11827 / EJ3) GN=mfnA PE=3 SV=1 | 65 | 457 | 2.0E-24 |
sp|Q8TUQ9|MFNA_METAC | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanosarcina acetivorans (strain ATCC 35395 / DSM 2834 / JCM 12185 / C2A) GN=mfnA PE=3 SV=1 | 88 | 460 | 7.0E-24 |
sp|Q5JJ82|MFNA_THEKO | L-aspartate decarboxylase OS=Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) GN=mfnA PE=1 SV=1 | 65 | 463 | 9.0E-24 |
sp|Q8PXA5|MFNA_METMA | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) GN=mfnA PE=3 SV=1 | 89 | 464 | 1.0E-23 |
sp|O28275|MFNA_ARCFU | Probable L-aspartate decarboxylase OS=Archaeoglobus fulgidus (strain ATCC 49558 / VC-16 / DSM 4304 / JCM 9628 / NBRC 100126) GN=mfnA PE=3 SV=1 | 98 | 374 | 2.0E-23 |
sp|A2STQ3|MFNA_METLZ | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanocorpusculum labreanum (strain ATCC 43576 / DSM 4855 / Z) GN=mfnA PE=3 SV=1 | 99 | 374 | 1.0E-22 |
sp|Q12VA2|MFNA_METBU | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanococcoides burtonii (strain DSM 6242 / NBRC 107633 / OCM 468 / ACE-M) GN=mfnA PE=3 SV=1 | 84 | 396 | 1.0E-22 |
sp|Q46DU3|MFNA_METBF | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanosarcina barkeri (strain Fusaro / DSM 804) GN=mfnA PE=3 SV=1 | 88 | 463 | 1.0E-22 |
sp|B8GDM7|MFNA_METPE | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanosphaerula palustris (strain ATCC BAA-1556 / DSM 19958 / E1-9c) GN=mfnA PE=3 SV=1 | 98 | 374 | 1.0E-22 |
sp|O27188|MFNA_METTH | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) GN=mfnA PE=3 SV=1 | 98 | 457 | 2.0E-22 |
sp|Q2NHY7|MFNA_METST | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanosphaera stadtmanae (strain ATCC 43021 / DSM 3091 / JCM 11832 / MCB-3) GN=mfnA PE=3 SV=1 | 101 | 461 | 3.0E-21 |
sp|A5ULW4|MFNA_METS3 | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanobrevibacter smithii (strain PS / ATCC 35061 / DSM 861) GN=mfnA PE=3 SV=1 | 86 | 456 | 5.0E-20 |
sp|Q2FSD2|MFNA_METHJ | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanospirillum hungatei JF-1 (strain ATCC 27890 / DSM 864 / NBRC 100397 / JF-1) GN=mfnA PE=3 SV=1 | 95 | 373 | 9.0E-20 |
sp|A7IAB9|MFNA_METB6 | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanoregula boonei (strain 6A8) GN=mfnA PE=3 SV=1 | 98 | 374 | 2.0E-19 |
sp|Q05567|SGPL_YEAST | Sphingosine-1-phosphate lyase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DPL1 PE=1 SV=1 | 108 | 375 | 3.0E-19 |
sp|Q54RV9|SGPL_DICDI | Sphingosine-1-phosphate lyase OS=Dictyostelium discoideum GN=sglA PE=2 SV=1 | 87 | 351 | 7.0E-18 |
sp|A3CWM4|MFNA_METMJ | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanoculleus marisnigri (strain ATCC 35101 / DSM 1498 / JR1) GN=mfnA PE=3 SV=1 | 98 | 374 | 2.0E-17 |
sp|Q52RG7|SGPL_ORYSJ | Sphingosine-1-phosphate lyase OS=Oryza sativa subsp. japonica GN=SPL PE=2 SV=2 | 87 | 452 | 2.0E-17 |
sp|Q9C509|SGPL_ARATH | Sphingosine-1-phosphate lyase OS=Arabidopsis thaliana GN=DPL1 PE=1 SV=1 | 93 | 446 | 6.0E-17 |
sp|A6URB4|MFNA_METVS | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanococcus vannielii (strain SB / ATCC 35089 / DSM 1224) GN=mfnA PE=3 SV=1 | 108 | 374 | 2.0E-16 |
sp|Q3IT46|MFNA_NATPD | Probable L-aspartate decarboxylase OS=Natronomonas pharaonis (strain ATCC 35678 / DSM 2160) GN=mfnA PE=3 SV=1 | 82 | 456 | 4.0E-16 |
sp|Q9Y194|SGPL_CAEEL | Sphingosine-1-phosphate lyase OS=Caenorhabditis elegans GN=spl-1 PE=1 SV=1 | 108 | 394 | 7.0E-16 |
sp|Q5V1B4|MFNA_HALMA | Probable L-aspartate decarboxylase OS=Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) GN=mfnA PE=3 SV=1 | 167 | 456 | 6.0E-15 |
sp|Q6M0Y7|MFNA_METMP | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanococcus maripaludis (strain S2 / LL) GN=mfnA PE=3 SV=1 | 108 | 374 | 2.0E-14 |
sp|Q8R0X7|SGPL1_MOUSE | Sphingosine-1-phosphate lyase 1 OS=Mus musculus GN=Sgpl1 PE=1 SV=1 | 108 | 419 | 2.0E-14 |
sp|O95470|SGPL1_HUMAN | Sphingosine-1-phosphate lyase 1 OS=Homo sapiens GN=SGPL1 PE=1 SV=3 | 108 | 419 | 3.0E-14 |
sp|Q60358|MFNA_METJA | L-tyrosine/L-aspartate decarboxylase OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=mfnA PE=1 SV=1 | 98 | 454 | 3.0E-14 |
sp|Q8CHN6|SGPL1_RAT | Sphingosine-1-phosphate lyase 1 OS=Rattus norvegicus GN=Sgpl1 PE=2 SV=1 | 108 | 419 | 5.0E-14 |
sp|A6UVR4|MFNA_META3 | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanococcus aeolicus (strain Nankai-3 / ATCC BAA-1280) GN=mfnA PE=3 SV=1 | 135 | 453 | 1.0E-13 |
sp|A4G060|MFNA_METM5 | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanococcus maripaludis (strain C5 / ATCC BAA-1333) GN=mfnA PE=3 SV=1 | 108 | 374 | 2.0E-13 |
sp|Q5WUR6|SGPL_LEGPL | Probable sphingosine-1-phosphate lyase OS=Legionella pneumophila (strain Lens) GN=lpl2102 PE=3 SV=1 | 105 | 372 | 3.0E-13 |
sp|Q5R4G0|SGPL1_PONAB | Sphingosine-1-phosphate lyase 1 OS=Pongo abelii GN=SGPL1 PE=2 SV=1 | 108 | 419 | 3.0E-13 |
sp|Q5ZTI6|SGPL_LEGPH | Probable sphingosine-1-phosphate lyase OS=Legionella pneumophila subsp. pneumophila (strain Philadelphia 1 / ATCC 33152 / DSM 7513) GN=lpg2176 PE=3 SV=2 | 105 | 372 | 3.0E-13 |
sp|A6VIC0|MFNA_METM7 | Probable L-tyrosine/L-aspartate decarboxylase OS=Methanococcus maripaludis (strain C7 / ATCC BAA-1331) GN=mfnA PE=3 SV=1 | 108 | 374 | 1.0E-12 |
sp|Q5X3A8|SGPL_LEGPA | Probable sphingosine-1-phosphate lyase OS=Legionella pneumophila (strain Paris) GN=lpp2128 PE=1 SV=1 | 105 | 372 | 1.0E-12 |
sp|Q9HSA3|MFNA_HALSA | Probable L-aspartate decarboxylase OS=Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) GN=mfnA PE=3 SV=1 | 171 | 442 | 5.0E-12 |
sp|B0R349|MFNA_HALS3 | Probable L-aspartate decarboxylase OS=Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) GN=mfnA PE=3 SV=1 | 171 | 442 | 5.0E-12 |
sp|Q9MA74|SDC1_ARATH | Serine decarboxylase OS=Arabidopsis thaliana GN=SDC PE=1 SV=1 | 184 | 449 | 3.0E-08 |
sp|Q8RV06|SDC2_ORYSJ | Serine decarboxylase 2 OS=Oryza sativa subsp. japonica GN=Os10g0105700 PE=2 SV=1 | 122 | 397 | 4.0E-08 |
sp|P54772|DCHS_SOLLC | Histidine decarboxylase OS=Solanum lycopersicum GN=HDC PE=2 SV=1 | 122 | 377 | 3.0E-07 |
sp|Q6ESZ9|SDC1_ORYSJ | Serine decarboxylase 1 OS=Oryza sativa subsp. japonica GN=SDC1 PE=3 SV=1 | 184 | 426 | 3.0E-07 |
GO Term | Description | Terminal node |
---|---|---|
GO:0016831 | carboxy-lyase activity | Yes |
GO:0030170 | pyridoxal phosphate binding | Yes |
GO:0019752 | carboxylic acid metabolic process | Yes |
GO:0044237 | cellular metabolic process | No |
GO:0003674 | molecular_function | No |
GO:0008144 | drug binding | No |
GO:0036094 | small molecule binding | No |
GO:0008150 | biological_process | No |
GO:0016829 | lyase activity | No |
GO:0008152 | metabolic process | No |
GO:0043436 | oxoacid metabolic process | No |
GO:0005488 | binding | No |
GO:0071704 | organic substance metabolic process | No |
GO:0097159 | organic cyclic compound binding | No |
GO:0009987 | cellular process | No |
GO:0048037 | cofactor binding | No |
GO:0050662 | coenzyme binding | No |
GO:0006082 | organic acid metabolic process | No |
GO:0016830 | carbon-carbon lyase activity | No |
GO:0070279 | vitamin B6 binding | No |
GO:0019842 | vitamin binding | No |
GO:0003824 | catalytic activity | No |
GO:0043168 | anion binding | No |
GO:0043167 | ion binding | No |
GO:0044281 | small molecule metabolic process | No |
GO:1901363 | heterocyclic compound binding | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 25 | 0.45 |
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|10848 MAHLTPKPADAVSHIAATPRDVSARQRHEEAATSVYGSRFATQGLPGTDMPDGPMPPTVAYRLIKDELSLDNNPK LNLATFVTTYMETEAEMLMNEAMSKNFIDYEEYPQTAEIHNRCSAMIANLFHASRDKSIGTSTVGSSEAIMLAVL ALKRRWKLRREAEGKPTDKPNIIMSSAVQVCWEKAARYFEIDARYVNCTRTRFTIDPKEAADLCDENTVAVVAIL GTTFTGAYEDVKGISDQLEKKGSDVPIHVDAASGGFVAPFVVPKLEWDFRVERVASINVSGHKYGLVYPGVGWVV WRSSEYLPSDLVFNINYLGAEQSSFTLNFSKGAAQIIGQYYQLIRLGKSGYRDIMCNLTQIADYLAESLREMGFI ILSETSGKALPLVAFRFPGRDEGAEEDQDFDEFALAHYLRIRGWVIPAYTMAPETERMKMMRVVVREDFSRSRCD QLVQDIKLCTQHLEKDSQQLLKRMQAQGVHVTAAGRTKNSLANAKEDFENEQHSLQGKSGKSHAIC* |
Coding | >Hirsu2|10848 ATGGCTCACCTGACGCCCAAGCCGGCGGACGCGGTCTCGCACATCGCCGCCACGCCGCGCGACGTGTCGGCCCGC CAGCGCCACGAAGAGGCCGCGACCAGTGTCTACGGCTCGCGCTTCGCCACTCAGGGCCTCCCCGGGACCGATATG CCGGACGGGCCCATGCCGCCGACTGTGGCCTACCGTCTGATCAAGGACGAGCTCAGCCTGGACAACAACCCCAAG CTCAACCTCGCAACCTTTGTGACGACCTACATGGAGACGGAGGCCGAGATGCTTATGAACGAGGCCATGTCGAAA AACTTCATCGACTACGAGGAGTATCCGCAGACGGCCGAGATTCACAACCGGTGCTCCGCCATGATCGCCAACCTG TTCCACGCGTCGCGCGATAAGTCGATCGGCACCTCGACCGTCGGCTCCTCCGAGGCCATCATGCTGGCCGTGCTC GCCCTCAAGCGGCGGTGGAAGCTGCGCCGCGAGGCCGAGGGCAAGCCGACCGATAAGCCCAACATCATCATGTCC TCGGCGGTGCAGGTCTGCTGGGAAAAGGCGGCGCGCTACTTCGAGATCGACGCCCGGTACGTCAACTGCACGCGG ACGCGCTTCACCATCGACCCCAAGGAGGCGGCGGACCTGTGCGACGAGAATACCGTGGCCGTCGTCGCCATCCTC GGCACTACCTTTACCGGCGCGTACGAGGACGTCAAGGGCATCAGTGACCAGCTCGAGAAGAAGGGGTCAGACGTG CCCATCCACGTCGACGCCGCCAGCGGCGGCTTCGTCGCCCCGTTCGTCGTCCCGAAGCTGGAATGGGACTTTCGA GTTGAGAGGGTGGCGTCGATCAACGTCTCCGGCCACAAGTACGGCCTCGTCTATCCCGGCGTCGGCTGGGTCGTG TGGCGGTCGTCCGAGTACCTGCCCTCGGACCTCGTCTTCAACATCAACTACCTCGGGGCCGAGCAGTCCTCCTTC ACGCTCAACTTCTCCAAGGGGGCGGCGCAGATCATCGGGCAGTACTACCAGCTGATCCGGCTCGGCAAGAGCGGC TACCGGGACATCATGTGCAACCTGACGCAGATCGCCGACTACCTGGCCGAGTCGCTGCGCGAGATGGGCTTCATC ATCCTGTCGGAGACGTCGGGCAAGGCGCTGCCGCTCGTCGCCTTCCGCTTCCCCGGGCGCGACGAGGGCGCCGAG GAGGACCAGGACTTTGACGAGTTCGCGCTGGCGCACTACCTGCGCATCCGCGGCTGGGTCATCCCGGCCTACACC ATGGCGCCCGAGACGGAGCGGATGAAGATGATGCGCGTCGTCGTCCGCGAGGACTTCTCGCGCAGCCGCTGCGAC CAGCTCGTCCAGGACATCAAGCTGTGCACCCAGCACCTCGAGAAGGACAGCCAGCAGCTGCTCAAGCGCATGCAG GCCCAGGGCGTCCACGTCACCGCCGCCGGCAGGACCAAGAACTCGCTGGCCAACGCCAAGGAAGACTTTGAGAAC GAACAACACTCTCTCCAGGGCAAGTCGGGCAAGAGCCACGCCATCTGCTAA |
Transcript | >Hirsu2|10848 ATGGCTCACCTGACGCCCAAGCCGGCGGACGCGGTCTCGCACATCGCCGCCACGCCGCGCGACGTGTCGGCCCGC CAGCGCCACGAAGAGGCCGCGACCAGTGTCTACGGCTCGCGCTTCGCCACTCAGGGCCTCCCCGGGACCGATATG CCGGACGGGCCCATGCCGCCGACTGTGGCCTACCGTCTGATCAAGGACGAGCTCAGCCTGGACAACAACCCCAAG CTCAACCTCGCAACCTTTGTGACGACCTACATGGAGACGGAGGCCGAGATGCTTATGAACGAGGCCATGTCGAAA AACTTCATCGACTACGAGGAGTATCCGCAGACGGCCGAGATTCACAACCGGTGCTCCGCCATGATCGCCAACCTG TTCCACGCGTCGCGCGATAAGTCGATCGGCACCTCGACCGTCGGCTCCTCCGAGGCCATCATGCTGGCCGTGCTC GCCCTCAAGCGGCGGTGGAAGCTGCGCCGCGAGGCCGAGGGCAAGCCGACCGATAAGCCCAACATCATCATGTCC TCGGCGGTGCAGGTCTGCTGGGAAAAGGCGGCGCGCTACTTCGAGATCGACGCCCGGTACGTCAACTGCACGCGG ACGCGCTTCACCATCGACCCCAAGGAGGCGGCGGACCTGTGCGACGAGAATACCGTGGCCGTCGTCGCCATCCTC GGCACTACCTTTACCGGCGCGTACGAGGACGTCAAGGGCATCAGTGACCAGCTCGAGAAGAAGGGGTCAGACGTG CCCATCCACGTCGACGCCGCCAGCGGCGGCTTCGTCGCCCCGTTCGTCGTCCCGAAGCTGGAATGGGACTTTCGA GTTGAGAGGGTGGCGTCGATCAACGTCTCCGGCCACAAGTACGGCCTCGTCTATCCCGGCGTCGGCTGGGTCGTG TGGCGGTCGTCCGAGTACCTGCCCTCGGACCTCGTCTTCAACATCAACTACCTCGGGGCCGAGCAGTCCTCCTTC ACGCTCAACTTCTCCAAGGGGGCGGCGCAGATCATCGGGCAGTACTACCAGCTGATCCGGCTCGGCAAGAGCGGC TACCGGGACATCATGTGCAACCTGACGCAGATCGCCGACTACCTGGCCGAGTCGCTGCGCGAGATGGGCTTCATC ATCCTGTCGGAGACGTCGGGCAAGGCGCTGCCGCTCGTCGCCTTCCGCTTCCCCGGGCGCGACGAGGGCGCCGAG GAGGACCAGGACTTTGACGAGTTCGCGCTGGCGCACTACCTGCGCATCCGCGGCTGGGTCATCCCGGCCTACACC ATGGCGCCCGAGACGGAGCGGATGAAGATGATGCGCGTCGTCGTCCGCGAGGACTTCTCGCGCAGCCGCTGCGAC CAGCTCGTCCAGGACATCAAGCTGTGCACCCAGCACCTCGAGAAGGACAGCCAGCAGCTGCTCAAGCGCATGCAG GCCCAGGGCGTCCACGTCACCGCCGCCGGCAGGACCAAGAACTCGCTGGCCAACGCCAAGGAAGACTTTGAGAAC GAACAACACTCTCTCCAGGGCAAGTCGGGCAAGAGCCACGCCATCTGCTAA |
Gene | >Hirsu2|10848 ATGGCTCACCTGACGCCCAAGCCGGCGGACGCGGTCTCGCACATCGCCGCCACGCCGCGCGACGTGTCGGCCCGC CAGCGCCACGAAGAGGCCGCGACCAGTGTCTACGGCTCGCGCTTCGCCACTCAGGGCCTCCCCGGGACCGATATG CCGGACGGGCCCATGCCGCCGACTGTGGCCTACCGTCTGATCAAGGACGAGCTCAGCCTGGACAACAACCCCAAG CTCAAGTCCGCCTCTCCCGCCCTCTCTCTTCTCCCCTCAAGGCTGACCGTTGCTGTCTTGGCCCCTCCCCGCCTG ACCAGCCTCGCAACCTTTGTGACGACCTACATGGTACGCTTCTCCCCGAGCGCCGCGAGCCGAGCGAGGGGCGTT GGACTGACGTGGCCGTGATCCCGCGGGGCAGGAGACGGAGGCCGAGATGCTTATGAACGAGGCCATGTCGAAAAA CTTCATCGACTACGAGGAGTATCCGCAGACGGCCGAGATTCACAACCGGTGCTCCGCCATGATCGCCAACCTGTT CCACGCGTCGCGCGATAAGTCGATCGGCACCTCGACCGTCGGCTCCTCCGAGGCCATCATGCTGGCCGTGCTCGC CCTCAAGCGGCGGTGGAAGCTGCGCCGCGAGGCCGAGGGCAAGCCGACCGATAAGCCCAACATCATCATGTCCTC GGCGGTGCAGGTCTGCTGGGAAAAGGCGGCGCGCTACTTCGAGATCGACGCCCGGTACGTCAACTGCACGCGGAC GCGCTTCACCATCGACCCCAAGGAGGCGGCGGACCTGTGCGACGAGAATACCGTGGCCGTCGTCGCCATCCTCGG CACTACCTTTACCGGCGCGTACGAGGACGTCAAGGGCATCAGTGACCAGCTCGAGAAGAAGGGGTCAGACGTGCC CATCCACGTCGACGCCGCCAGCGGCGGCTTCGTCGCCCCGTTCGTCGTCCCGAAGCTGGAATGGGACTTTCGAGT TGAGAGGGTGGCGTCGATCAACGTCTCCGGCCACAAGGTATGTCGCGGCTGTCGACCCCCTTGTTCCCGATAAGG CGATGCCGAAGCCTGACCCTTGTTCTTCTCCTTCTCCTTCTTCGTCTTCTTCAGTACGGCCTCGTCTATCCCGGC GTCGGCTGGGTCGTGTGGCGGTCGTCCGAGTACCTGCCCTCGGACCTCGTCTTCAACATCAACTACCTCGGGGCC GAGCAGTCCTCCTTCACGCTCAACTTCTCCAAGGGGGCGGCGCAGATCATCGGGCAGTACTACCAGCTGATCCGG CTCGGCAAGAGCGGCTACCGGGACATCATGTGCAACCTGACGCAGATCGCCGACTACCTGGCCGAGTCGCTGCGC GAGATGGGCTTCATCATCCTGTCGGAGACGTCGGGCAAGGCGCTGCCGCTCGTCGCCTTCCGCTTCCCCGGGCGC GACGAGGGCGCCGAGGAGGACCAGGACTTTGACGAGTTCGCGCTGGCGCACTACCTGCGCATCCGCGGCTGGGTC ATCCCGGCCTACACCATGGCGCCCGAGACGGAGCGGATGAAGATGATGCGCGTCGTCGTCCGCGAGGACTTCTCG CGCAGCCGCTGCGACCAGCTCGTCCAGGACATCAAGCTGTGCACCCAGCACCTCGAGAAGGACAGCCAGCAGCTG CTCAAGCGCATGCAGGCCCAGGGCGTCCACGTCACCGCCGCCGGCAGGACCAAGAACTCGCTGGCCAACGCCAAG GAAGACTTTGAGGTATGTCTTACTCCTTCTCCGTCAGAGACGACGAGGCGGAAGCTGCTGAGCCGAGCTGACCAC GAGCTGCCGCCAGAACGAACAACACTCTCTCCAGGGCAAGTCGGGCAAGAGCCACGCCATCTGCTAA |