Protein ID | Hirsu2|3649 |
Gene name | |
Location | Contig_1977:2128..3625 |
Strand | + |
Gene length (bp) | 1497 |
Transcript length (bp) | 1497 |
Coding sequence length (bp) | 1497 |
Protein length (aa) | 499 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00481 | PP2C | Protein phosphatase 2C | 3.6E-29 | 286 | 448 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|O14156|PP2C4_SCHPO | Protein phosphatase 2C homolog 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc4 PE=1 SV=2 | 51 | 495 | 4.0E-44 |
sp|Q8BXN7|PPM1K_MOUSE | Protein phosphatase 1K, mitochondrial OS=Mus musculus GN=Ppm1k PE=1 SV=1 | 277 | 466 | 5.0E-24 |
sp|Q6ING9|PPM1K_XENLA | Protein phosphatase 1K, mitochondrial OS=Xenopus laevis GN=ppm1k PE=2 SV=1 | 282 | 466 | 8.0E-24 |
sp|Q8N3J5|PPM1K_HUMAN | Protein phosphatase 1K, mitochondrial OS=Homo sapiens GN=PPM1K PE=1 SV=1 | 282 | 466 | 9.0E-24 |
sp|Q2PC20|PPM1K_BOVIN | Protein phosphatase 1K, mitochondrial OS=Bos taurus GN=PPM1K PE=2 SV=1 | 277 | 466 | 9.0E-24 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|O14156|PP2C4_SCHPO | Protein phosphatase 2C homolog 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc4 PE=1 SV=2 | 51 | 495 | 4.0E-44 |
sp|Q8BXN7|PPM1K_MOUSE | Protein phosphatase 1K, mitochondrial OS=Mus musculus GN=Ppm1k PE=1 SV=1 | 277 | 466 | 5.0E-24 |
sp|Q6ING9|PPM1K_XENLA | Protein phosphatase 1K, mitochondrial OS=Xenopus laevis GN=ppm1k PE=2 SV=1 | 282 | 466 | 8.0E-24 |
sp|Q8N3J5|PPM1K_HUMAN | Protein phosphatase 1K, mitochondrial OS=Homo sapiens GN=PPM1K PE=1 SV=1 | 282 | 466 | 9.0E-24 |
sp|Q2PC20|PPM1K_BOVIN | Protein phosphatase 1K, mitochondrial OS=Bos taurus GN=PPM1K PE=2 SV=1 | 277 | 466 | 9.0E-24 |
sp|P25646|PDP2_YEAST | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 2, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC6 PE=1 SV=2 | 313 | 466 | 5.0E-20 |
sp|Q8L7I4|P2C17_ARATH | Probable protein phosphatase 2C 17 OS=Arabidopsis thaliana GN=At1g78200 PE=2 SV=1 | 287 | 463 | 2.0E-15 |
sp|Q0JAA0|P2C44_ORYSJ | Probable protein phosphatase 2C 44 OS=Oryza sativa subsp. japonica GN=Os04g0609600 PE=2 SV=1 | 287 | 463 | 6.0E-15 |
sp|Q8RXV3|P2C59_ARATH | Probable protein phosphatase 2C 59 OS=Arabidopsis thaliana GN=WIN2 PE=1 SV=1 | 288 | 480 | 1.0E-14 |
sp|Q4PSE8|P2C71_ARATH | Probable protein phosphatase 2C 71 OS=Arabidopsis thaliana GN=At5g24940 PE=2 SV=1 | 288 | 463 | 3.0E-14 |
sp|Q7XR06|P2C45_ORYSJ | Probable protein phosphatase 2C 45 OS=Oryza sativa subsp. japonica GN=Os04g0659500 PE=2 SV=2 | 288 | 463 | 1.0E-13 |
sp|Q67UX7|P2C10_ORYSJ | Probable protein phosphatase 2C 10 OS=Oryza sativa subsp. japonica GN=Os02g0149800 PE=2 SV=1 | 288 | 463 | 1.0E-13 |
sp|Q0JL75|P2C07_ORYSJ | Probable protein phosphatase 2C 7 OS=Oryza sativa subsp. japonica GN=Os01g0618200 PE=2 SV=2 | 288 | 463 | 1.0E-13 |
sp|Q8BHN0|PPM1L_MOUSE | Protein phosphatase 1L OS=Mus musculus GN=Ppm1l PE=1 SV=1 | 286 | 463 | 2.0E-13 |
sp|Q5SGD2|PPM1L_HUMAN | Protein phosphatase 1L OS=Homo sapiens GN=PPM1L PE=1 SV=1 | 286 | 463 | 2.0E-13 |
sp|Q8VZN9|P2C11_ARATH | Probable protein phosphatase 2C 11 OS=Arabidopsis thaliana GN=At1g43900 PE=2 SV=1 | 313 | 463 | 4.0E-13 |
sp|Q5Z6F5|P2C59_ORYSJ | Probable protein phosphatase 2C 59 OS=Oryza sativa subsp. japonica GN=Os06g0698300 PE=2 SV=1 | 288 | 463 | 5.0E-13 |
sp|A5PJZ2|PPM1L_BOVIN | Protein phosphatase 1L OS=Bos taurus GN=PPM1L PE=2 SV=1 | 286 | 463 | 5.0E-13 |
sp|P40371|PP2C1_SCHPO | Protein phosphatase 2C homolog 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc1 PE=2 SV=1 | 288 | 463 | 1.0E-12 |
sp|Q6L5C4|P2C52_ORYSJ | Probable protein phosphatase 2C 52 OS=Oryza sativa subsp. japonica GN=Os05g0587100 PE=2 SV=1 | 288 | 463 | 1.0E-12 |
sp|Q53Q11|P2C74_ORYSJ | Probable protein phosphatase 2C 74 OS=Oryza sativa subsp. japonica GN=Os11g0242200 PE=3 SV=1 | 286 | 463 | 2.0E-12 |
sp|Q9LDA7|P2C39_ARATH | Probable protein phosphatase 2C 39 OS=Arabidopsis thaliana GN=At3g15260 PE=2 SV=1 | 286 | 463 | 2.0E-12 |
sp|Q93YW5|P2C58_ARATH | Probable protein phosphatase 2C 58 OS=Arabidopsis thaliana GN=At4g28400 PE=2 SV=1 | 286 | 463 | 5.0E-12 |
sp|Q8LAY8|P2C69_ARATH | Probable protein phosphatase 2C 69 OS=Arabidopsis thaliana GN=At5g10740 PE=2 SV=1 | 288 | 463 | 6.0E-12 |
sp|Q6Z8B9|P2C12_ORYSJ | Probable protein phosphatase 2C 12 OS=Oryza sativa subsp. japonica GN=Os02g0224100 PE=2 SV=1 | 313 | 451 | 1.0E-11 |
sp|Q9SIU8|P2C20_ARATH | Probable protein phosphatase 2C 20 OS=Arabidopsis thaliana GN=PPC3-1.2 PE=1 SV=3 | 286 | 460 | 2.0E-11 |
sp|Q94AT1|P2C76_ARATH | Probable protein phosphatase 2C 76 OS=Arabidopsis thaliana GN=At5g53140 PE=2 SV=1 | 288 | 463 | 3.0E-11 |
sp|Q0D673|P2C62_ORYSJ | Probable protein phosphatase 2C 62 OS=Oryza sativa subsp. japonica GN=Os07g0507000 PE=2 SV=1 | 286 | 463 | 5.0E-11 |
sp|Q653S3|P2C70_ORYSJ | Probable protein phosphatase 2C 70 OS=Oryza sativa subsp. japonica GN=Os09g0558000 PE=2 SV=2 | 288 | 463 | 7.0E-11 |
sp|Q7XQU7|P2C41_ORYSJ | Probable protein phosphatase 2C 41 OS=Oryza sativa subsp. japonica GN=Os04g0452000 PE=2 SV=2 | 286 | 463 | 1.0E-10 |
sp|Q6EN45|P2C13_ORYSJ | Probable protein phosphatase 2C 13 OS=Oryza sativa subsp. japonica GN=Os02g0255100 PE=2 SV=1 | 313 | 463 | 1.0E-10 |
sp|Q5R522|PPM1K_PONAB | Protein phosphatase 1K, mitochondrial OS=Pongo abelii GN=PPM1K PE=2 SV=1 | 282 | 425 | 2.0E-10 |
sp|Q9XGZ9|P2C72_ARATH | Probable protein phosphatase 2C 72 OS=Arabidopsis thaliana GN=At5g26010 PE=2 SV=2 | 313 | 429 | 3.0E-10 |
sp|Q2RBJ6|P2C73_ORYSJ | Probable protein phosphatase 2C 73 OS=Oryza sativa subsp. japonica GN=Os11g0109000 PE=2 SV=1 | 313 | 451 | 4.0E-10 |
sp|P49444|PP2C1_PARTE | Protein phosphatase 2C 1 OS=Paramecium tetraurelia GN=GSPATT00029903001 PE=1 SV=2 | 288 | 448 | 6.0E-10 |
sp|Q9XEE8|P2C30_ARATH | Probable protein phosphatase 2C 30 OS=Arabidopsis thaliana GN=PP2C5 PE=2 SV=1 | 286 | 430 | 6.0E-10 |
sp|Q2R637|P2C75_ORYSJ | Probable protein phosphatase 2C 75 OS=Oryza sativa subsp. japonica GN=Os11g0417400 PE=2 SV=1 | 313 | 451 | 7.0E-10 |
sp|Q0IIF0|ILKAP_BOVIN | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Bos taurus GN=ILKAP PE=2 SV=1 | 285 | 464 | 9.0E-10 |
sp|P35182|PP2C1_YEAST | Protein phosphatase 2C homolog 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC1 PE=1 SV=1 | 286 | 463 | 1.0E-09 |
sp|Q9H0C8|ILKAP_HUMAN | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Homo sapiens GN=ILKAP PE=1 SV=1 | 303 | 464 | 2.0E-09 |
sp|Q8H4S6|P2C64_ORYSJ | Probable protein phosphatase 2C 64 OS=Oryza sativa subsp. japonica GN=Os07g0566200 PE=2 SV=2 | 311 | 447 | 3.0E-09 |
sp|Q8R0F6|ILKAP_MOUSE | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Mus musculus GN=Ilkap PE=1 SV=1 | 303 | 464 | 3.0E-09 |
sp|Q9Z1Z6|ILKAP_RAT | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Rattus norvegicus GN=Ilkap PE=2 SV=1 | 295 | 464 | 3.0E-09 |
sp|O82637|P2C61_ARATH | Probable protein phosphatase 2C 61 OS=Arabidopsis thaliana GN=At4g32950 PE=3 SV=1 | 313 | 448 | 5.0E-09 |
sp|Q54WS9|Y9461_DICDI | Probable protein phosphatase DDB_G0279461 OS=Dictyostelium discoideum GN=DDB_G0279461 PE=3 SV=2 | 288 | 463 | 5.0E-09 |
sp|O64583|P2C28_ARATH | Probable protein phosphatase 2C 28 OS=Arabidopsis thaliana GN=At2g34740 PE=2 SV=2 | 286 | 466 | 8.0E-09 |
sp|O80871|P2C25_ARATH | Probable protein phosphatase 2C 25 OS=Arabidopsis thaliana GN=At2g30020 PE=1 SV=1 | 286 | 430 | 1.0E-08 |
sp|Q2QWE3|P2C77_ORYSJ | Probable protein phosphatase 2C 77 OS=Oryza sativa subsp. japonica GN=Os12g0198200 PE=3 SV=1 | 285 | 424 | 1.0E-08 |
sp|Q9S9Z7|P2C10_ARATH | Probable protein phosphatase 2C 10 OS=Arabidopsis thaliana GN=At1g34750 PE=2 SV=1 | 286 | 463 | 1.0E-08 |
sp|P39966|PP2C2_YEAST | Protein phosphatase 2C homolog 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC2 PE=1 SV=1 | 288 | 487 | 2.0E-08 |
sp|Q8RXZ4|P2C18_ARATH | Probable protein phosphatase 2C 18 OS=Arabidopsis thaliana GN=At1g79630 PE=2 SV=1 | 313 | 463 | 2.0E-08 |
sp|Q7XW27|P2C38_ORYSJ | Probable protein phosphatase 2C 38 OS=Oryza sativa subsp. japonica GN=Os04g0321800 PE=2 SV=2 | 313 | 451 | 2.0E-08 |
sp|Q3EAF9|P2C49_ARATH | Probable protein phosphatase 2C 49 OS=Arabidopsis thaliana GN=At3g62260 PE=2 SV=1 | 313 | 468 | 3.0E-08 |
sp|F1LNI5|PPM1G_RAT | Protein phosphatase 1G OS=Rattus norvegicus GN=Ppm1g PE=1 SV=2 | 288 | 461 | 3.0E-08 |
sp|O15355|PPM1G_HUMAN | Protein phosphatase 1G OS=Homo sapiens GN=PPM1G PE=1 SV=1 | 288 | 461 | 3.0E-08 |
sp|Q9SA22|P2C06_ARATH | Probable protein phosphatase 2C 6 OS=Arabidopsis thaliana GN=At1g16220 PE=2 SV=1 | 313 | 463 | 3.0E-08 |
sp|Q4R4V2|PPM1G_MACFA | Protein phosphatase 1G OS=Macaca fascicularis GN=PPM1G PE=2 SV=1 | 288 | 461 | 3.0E-08 |
sp|Q0WRB2|P2C73_ARATH | Probable protein phosphatase 2C 73 OS=Arabidopsis thaliana GN=PPC6-7 PE=2 SV=1 | 312 | 447 | 3.0E-08 |
sp|Q61074|PPM1G_MOUSE | Protein phosphatase 1G OS=Mus musculus GN=Ppm1g PE=1 SV=3 | 288 | 461 | 4.0E-08 |
sp|P79126|PPM1G_BOVIN | Protein phosphatase 1G OS=Bos taurus GN=PPM1G PE=2 SV=2 | 288 | 461 | 4.0E-08 |
sp|P49596|PP2C2_CAEEL | Probable protein phosphatase 2C T23F11.1 OS=Caenorhabditis elegans GN=ppm-2 PE=3 SV=2 | 288 | 431 | 5.0E-08 |
sp|Q67UP9|P2C58_ORYSJ | Probable protein phosphatase 2C 58 OS=Oryza sativa subsp. japonica GN=Os06g0651600 PE=2 SV=1 | 288 | 431 | 6.0E-08 |
sp|Q5JJY4|P2C04_ORYSJ | Protein kinase and PP2C-like domain-containing protein OS=Oryza sativa subsp. japonica GN=Os01g0541900 PE=2 SV=1 | 305 | 463 | 6.0E-08 |
sp|Q8GY60|P2C52_ARATH | Probable protein phosphatase 2C 52 OS=Arabidopsis thaliana GN=At4g03415 PE=2 SV=1 | 311 | 446 | 6.0E-08 |
sp|Q84JI0|P2C30_ORYSJ | Probable protein phosphatase 2C 30 OS=Oryza sativa subsp. japonica GN=Os03g0268600 PE=2 SV=1 | 313 | 430 | 7.0E-08 |
sp|Q9LNW3|P2C03_ARATH | Protein phosphatase 2C 3 OS=Arabidopsis thaliana GN=AIP1 PE=1 SV=1 | 288 | 430 | 8.0E-08 |
sp|A3CCP9|P2C76_ORYSJ | Putative protein phosphatase 2C 76 OS=Oryza sativa subsp. japonica GN=Os11g0586001 PE=3 SV=2 | 283 | 464 | 1.0E-07 |
sp|Q9FXE4|P2C14_ARATH | Probable protein phosphatase 2C 14 OS=Arabidopsis thaliana GN=At1g67820 PE=2 SV=2 | 313 | 437 | 1.0E-07 |
sp|Q7XU84|P2C42_ORYSJ | Probable protein phosphatase 2C 42 OS=Oryza sativa subsp. japonica GN=Os04g0500900 PE=3 SV=4 | 288 | 430 | 2.0E-07 |
sp|P49443|PPM1A_MOUSE | Protein phosphatase 1A OS=Mus musculus GN=Ppm1a PE=1 SV=1 | 286 | 430 | 2.0E-07 |
sp|P35813|PPM1A_HUMAN | Protein phosphatase 1A OS=Homo sapiens GN=PPM1A PE=1 SV=1 | 286 | 430 | 2.0E-07 |
sp|P35814|PPM1A_RABIT | Protein phosphatase 1A OS=Oryctolagus cuniculus GN=PPM1A PE=2 SV=1 | 286 | 430 | 2.0E-07 |
sp|P20650|PPM1A_RAT | Protein phosphatase 1A OS=Rattus norvegicus GN=Ppm1a PE=1 SV=1 | 286 | 430 | 2.0E-07 |
sp|Q9FG61|P2C74_ARATH | Probable protein phosphatase 2C 74 OS=Arabidopsis thaliana GN=At5g36250 PE=1 SV=1 | 313 | 447 | 2.0E-07 |
sp|Q9M9W9|P2C34_ARATH | Probable protein phosphatase 2C 34 OS=Arabidopsis thaliana GN=At3g05640 PE=2 SV=1 | 312 | 447 | 3.0E-07 |
sp|O62829|PPM1A_BOVIN | Protein phosphatase 1A OS=Bos taurus GN=PPM1A PE=2 SV=1 | 286 | 430 | 3.0E-07 |
sp|Q65XK7|P2C51_ORYSJ | Probable protein phosphatase 2C 51 OS=Oryza sativa subsp. japonica GN=Os05g0572700 PE=2 SV=1 | 288 | 423 | 3.0E-07 |
sp|Q9FLI3|P2C75_ARATH | Probable protein phosphatase 2C 75 OS=Arabidopsis thaliana GN=AHG1 PE=2 SV=1 | 313 | 430 | 9.0E-07 |
sp|Q9LR65|P2C01_ARATH | Probable protein phosphatase 2C 1 OS=Arabidopsis thaliana GN=PPC6-6 PE=1 SV=1 | 311 | 447 | 2.0E-06 |
sp|Q5SN75|P2C08_ORYSJ | Probable protein phosphatase 2C 8 OS=Oryza sativa subsp. japonica GN=Os01g0656200 PE=2 SV=1 | 313 | 422 | 2.0E-06 |
sp|Q9ZW21|P2C24_ARATH | Probable protein phosphatase 2C 24 OS=Arabidopsis thaliana GN=At2g29380 PE=2 SV=1 | 289 | 430 | 3.0E-06 |
sp|Q8H2T0|P2C65_ORYSJ | Probable protein phosphatase 2C 65 OS=Oryza sativa subsp. japonica GN=Os07g0646100 PE=2 SV=1 | 315 | 457 | 4.0E-06 |
sp|Q84JD5|P2C68_ARATH | Probable protein phosphatase 2C 68 OS=Arabidopsis thaliana GN=At5g06750 PE=2 SV=1 | 310 | 450 | 6.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0004722 | protein serine/threonine phosphatase activity | Yes |
GO:0140096 | catalytic activity, acting on a protein | No |
GO:0003824 | catalytic activity | No |
GO:0016791 | phosphatase activity | No |
GO:0016787 | hydrolase activity | No |
GO:0016788 | hydrolase activity, acting on ester bonds | No |
GO:0042578 | phosphoric ester hydrolase activity | No |
GO:0003674 | molecular_function | No |
GO:0004721 | phosphoprotein phosphatase activity | No |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Cytoplasm | 0.5079 | 0.3485 | 0.0662 | 0.1083 | 0.2049 | 0.0058 | 0.1961 | 0.1378 | 0.1481 | 0.0614 |
Orthofinder run ID | 4 |
Orthogroup | 2505 |
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|3649 LPSSSLHPDSRISVGPSHKLPRDASTPHTPGPGSSLAVSLPNMPGRELTVVRIPLRRAKHHFGSYTSRGSRPYNE DTDQAGIVEIPAFAKRAPMSVKQKPGEATPADGASGDPQVFYFALFDGHGGSQCSHFLRDELHGYIEEAVAEFGL QSSLRKTKPGREARAFPSDAARGAAESPVAGDAQDRAKAMRLERELVEAYRNTIGGYFKRFVPEHFALQEGAERS ACAVESSLVYAFLRADLDFVSAQARKRDPDDSDMPLNNDEILGAPHAPPSGHGIGGATRFKGGSTASVALISTPT PAPFWHPGAQSTLLVAHVGDSRVLLCETATGRAQPLTSDHHPTTPTESRRLRRYAPAGSLVTGDSFGEERIAGLA NSRPFGDIRSKRIGVSAEPELARVDMGPAQYAFLVLVSDGVSGTLSDQEIVDVVKEARTPDQGARALVDYATEVS RDGDNATCQVVRLGGWERRSEGGLGSLGTKEVRDARRAEAQDPRRGKR* |
Coding | >Hirsu2|3649 CTGCCGTCGTCGTCGCTCCACCCCGACTCGCGCATCTCCGTCGGTCCAAGCCACAAGCTGCCCCGCGATGCCTCG ACGCCTCACACGCCGGGGCCCGGATCCTCTCTCGCCGTCTCCCTGCCCAACATGCCGGGCCGGGAGCTGACGGTC GTGAGGATCCCGCTGAGGCGGGCCAAGCATCACTTCGGCTCGTACACGAGCAGAGGCAGCCGGCCCTACAACGAG GACACGGACCAGGCCGGCATCGTCGAGATCCCGGCCTTTGCCAAGAGGGCGCCCATGAGCGTCAAGCAGAAGCCC GGAGAGGCGACGCCGGCCGACGGCGCCAGCGGCGACCCCCAGGTCTTCTACTTCGCCCTCTTCGACGGGCACGGC GGGTCGCAGTGCTCGCACTTCCTGCGCGACGAACTGCACGGCTACATCGAGGAGGCCGTGGCCGAGTTCGGCCTG CAGAGCAGTCTGCGCAAGACGAAGCCCGGACGCGAGGCGCGCGCCTTCCCCTCGGACGCCGCCCGCGGCGCCGCC GAGAGCCCCGTAGCGGGCGACGCGCAGGACCGCGCCAAGGCGATGCGGCTGGAGAGGGAGCTGGTCGAGGCGTAC CGGAACACCATCGGCGGCTACTTCAAGCGCTTCGTGCCCGAGCACTTCGCGCTGCAGGAGGGGGCGGAGAGGTCG GCGTGCGCGGTGGAGTCGAGCCTGGTGTACGCCTTCCTGCGGGCCGACCTGGACTTCGTGTCGGCGCAGGCGCGC AAGCGGGACCCGGACGACTCGGACATGCCGCTCAACAACGACGAGATCCTGGGGGCGCCGCACGCGCCGCCGTCG GGCCACGGCATCGGCGGCGCGACGCGCTTCAAGGGCGGGTCGACGGCGTCGGTGGCGCTCATCTCGACGCCGACG CCGGCGCCCTTCTGGCACCCGGGCGCGCAGTCGACGCTGCTGGTGGCGCACGTGGGCGACAGCCGGGTGCTGCTG TGCGAGACGGCGACGGGGCGCGCGCAGCCGCTGACGTCGGACCACCACCCGACGACGCCGACGGAGAGCCGGCGC CTGCGCCGCTACGCGCCCGCCGGCTCGCTCGTCACGGGCGACAGCTTCGGCGAGGAGCGCATCGCCGGCCTGGCC AACAGCCGCCCCTTCGGCGACATCCGCAGCAAGCGCATCGGCGTCTCGGCCGAGCCCGAGCTGGCCCGCGTCGAC ATGGGCCCGGCCCAGTACGCCTTCCTCGTCCTCGTCAGCGACGGCGTCTCCGGCACCCTCAGCGACCAGGAGATC GTCGACGTCGTCAAGGAGGCCCGCACCCCGGACCAGGGCGCCCGCGCCCTCGTCGACTACGCCACCGAGGTCTCG CGCGACGGCGACAACGCCACCTGCCAGGTCGTCCGCCTCGGCGGCTGGGAGCGCCGCTCCGAGGGCGGCCTCGGC AGCCTCGGCACCAAGGAGGTCCGCGACGCCCGCAGGGCCGAGGCCCAGGACCCGCGCCGCGGCAAGCGCTGA |
Transcript | >Hirsu2|3649 CTGCCGTCGTCGTCGCTCCACCCCGACTCGCGCATCTCCGTCGGTCCAAGCCACAAGCTGCCCCGCGATGCCTCG ACGCCTCACACGCCGGGGCCCGGATCCTCTCTCGCCGTCTCCCTGCCCAACATGCCGGGCCGGGAGCTGACGGTC GTGAGGATCCCGCTGAGGCGGGCCAAGCATCACTTCGGCTCGTACACGAGCAGAGGCAGCCGGCCCTACAACGAG GACACGGACCAGGCCGGCATCGTCGAGATCCCGGCCTTTGCCAAGAGGGCGCCCATGAGCGTCAAGCAGAAGCCC GGAGAGGCGACGCCGGCCGACGGCGCCAGCGGCGACCCCCAGGTCTTCTACTTCGCCCTCTTCGACGGGCACGGC GGGTCGCAGTGCTCGCACTTCCTGCGCGACGAACTGCACGGCTACATCGAGGAGGCCGTGGCCGAGTTCGGCCTG CAGAGCAGTCTGCGCAAGACGAAGCCCGGACGCGAGGCGCGCGCCTTCCCCTCGGACGCCGCCCGCGGCGCCGCC GAGAGCCCCGTAGCGGGCGACGCGCAGGACCGCGCCAAGGCGATGCGGCTGGAGAGGGAGCTGGTCGAGGCGTAC CGGAACACCATCGGCGGCTACTTCAAGCGCTTCGTGCCCGAGCACTTCGCGCTGCAGGAGGGGGCGGAGAGGTCG GCGTGCGCGGTGGAGTCGAGCCTGGTGTACGCCTTCCTGCGGGCCGACCTGGACTTCGTGTCGGCGCAGGCGCGC AAGCGGGACCCGGACGACTCGGACATGCCGCTCAACAACGACGAGATCCTGGGGGCGCCGCACGCGCCGCCGTCG GGCCACGGCATCGGCGGCGCGACGCGCTTCAAGGGCGGGTCGACGGCGTCGGTGGCGCTCATCTCGACGCCGACG CCGGCGCCCTTCTGGCACCCGGGCGCGCAGTCGACGCTGCTGGTGGCGCACGTGGGCGACAGCCGGGTGCTGCTG TGCGAGACGGCGACGGGGCGCGCGCAGCCGCTGACGTCGGACCACCACCCGACGACGCCGACGGAGAGCCGGCGC CTGCGCCGCTACGCGCCCGCCGGCTCGCTCGTCACGGGCGACAGCTTCGGCGAGGAGCGCATCGCCGGCCTGGCC AACAGCCGCCCCTTCGGCGACATCCGCAGCAAGCGCATCGGCGTCTCGGCCGAGCCCGAGCTGGCCCGCGTCGAC ATGGGCCCGGCCCAGTACGCCTTCCTCGTCCTCGTCAGCGACGGCGTCTCCGGCACCCTCAGCGACCAGGAGATC GTCGACGTCGTCAAGGAGGCCCGCACCCCGGACCAGGGCGCCCGCGCCCTCGTCGACTACGCCACCGAGGTCTCG CGCGACGGCGACAACGCCACCTGCCAGGTCGTCCGCCTCGGCGGCTGGGAGCGCCGCTCCGAGGGCGGCCTCGGC AGCCTCGGCACCAAGGAGGTCCGCGACGCCCGCAGGGCCGAGGCCCAGGACCCGCGCCGCGGCAAGCGCTGA |
Gene | >Hirsu2|3649 CTGCCGTCGTCGTCGCTCCACCCCGACTCGCGCATCTCCGTCGGTCCAAGCCACAAGCTGCCCCGCGATGCCTCG ACGCCTCACACGCCGGGGCCCGGATCCTCTCTCGCCGTCTCCCTGCCCAACATGCCGGGCCGGGAGCTGACGGTC GTGAGGATCCCGCTGAGGCGGGCCAAGCATCACTTCGGCTCGTACACGAGCAGAGGCAGCCGGCCCTACAACGAG GACACGGACCAGGCCGGCATCGTCGAGATCCCGGCCTTTGCCAAGAGGGCGCCCATGAGCGTCAAGCAGAAGCCC GGAGAGGCGACGCCGGCCGACGGCGCCAGCGGCGACCCCCAGGTCTTCTACTTCGCCCTCTTCGACGGGCACGGC GGGTCGCAGTGCTCGCACTTCCTGCGCGACGAACTGCACGGCTACATCGAGGAGGCCGTGGCCGAGTTCGGCCTG CAGAGCAGTCTGCGCAAGACGAAGCCCGGACGCGAGGCGCGCGCCTTCCCCTCGGACGCCGCCCGCGGCGCCGCC GAGAGCCCCGTAGCGGGCGACGCGCAGGACCGCGCCAAGGCGATGCGGCTGGAGAGGGAGCTGGTCGAGGCGTAC CGGAACACCATCGGCGGCTACTTCAAGCGCTTCGTGCCCGAGCACTTCGCGCTGCAGGAGGGGGCGGAGAGGTCG GCGTGCGCGGTGGAGTCGAGCCTGGTGTACGCCTTCCTGCGGGCCGACCTGGACTTCGTGTCGGCGCAGGCGCGC AAGCGGGACCCGGACGACTCGGACATGCCGCTCAACAACGACGAGATCCTGGGGGCGCCGCACGCGCCGCCGTCG GGCCACGGCATCGGCGGCGCGACGCGCTTCAAGGGCGGGTCGACGGCGTCGGTGGCGCTCATCTCGACGCCGACG CCGGCGCCCTTCTGGCACCCGGGCGCGCAGTCGACGCTGCTGGTGGCGCACGTGGGCGACAGCCGGGTGCTGCTG TGCGAGACGGCGACGGGGCGCGCGCAGCCGCTGACGTCGGACCACCACCCGACGACGCCGACGGAGAGCCGGCGC CTGCGCCGCTACGCGCCCGCCGGCTCGCTCGTCACGGGCGACAGCTTCGGCGAGGAGCGCATCGCCGGCCTGGCC AACAGCCGCCCCTTCGGCGACATCCGCAGCAAGCGCATCGGCGTCTCGGCCGAGCCCGAGCTGGCCCGCGTCGAC ATGGGCCCGGCCCAGTACGCCTTCCTCGTCCTCGTCAGCGACGGCGTCTCCGGCACCCTCAGCGACCAGGAGATC GTCGACGTCGTCAAGGAGGCCCGCACCCCGGACCAGGGCGCCCGCGCCCTCGTCGACTACGCCACCGAGGTCTCG CGCGACGGCGACAACGCCACCTGCCAGGTCGTCCGCCTCGGCGGCTGGGAGCGCCGCTCCGAGGGCGGCCTCGGC AGCCTCGGCACCAAGGAGGTCCGCGACGCCCGCAGGGCCGAGGCCCAGGACCCGCGCCGCGGCAAGCGCTGA |