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TRY gene, located at Chromosome 11.q23, is the most sever form of albinism caused by mutation in the tyrosinase gene . Variation is this gene can causes OCA type 1
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| >NM_000372.5 Homo sapiens tyrosinase (TYR), mRNA | ||
| ACTGTAGTAGTAGCTGGAAAGAGAAATCTGTGACTCCAATTAGCCAGTTCCTGCAGACCT | ||
| TGTGAGGACTAGAGGAAGAATGCTCCTGGCTGTTTTGTACTGCCTGCTGTGGAGTTTCCA | ||
| GACCTCCGCTGGCCATTTCCCTAGAGCCTGTGTCTCCTCTAAGAACCTGATGGAGAAGGA | ||
| ATGCTGTCCACCGTGGAGCGGGGACAGGAGTCCCTGTGGCCAGCTTTCAGGCAGAGGTTC | ||
| CTGTCAGAATATCCTTCTGTCCAATGCACCACTTGGGCCTCAATTTCCCTTCACAGGGGT | ||
| GGATGACCGGGAGTCGTGGCCTTCCGTCTTTTATAATAGGACCTGCCAGTGCTCTGGCAA | ||
| CTTCATGGGATTCAACTGTGGAAACTGCAAGTTTGGCTTTTGGGGACCAAACTGCACAGA | ||
| GAGACGACTCTTGGTGAGAAGAAACATCTTCGATTTGAGTGCCCCAGAGAAGGACAAATT | ||
| TTTTGCCTACCTCACTTTAGCAAAGCATACCATCAGCTCAGACTATGTCATCCCCATAGG | ||
| GACCTATGGCCAAATGAAAAATGGATCAACACCCATGTTTAACGACATCAATATTTATGA | ||
| CCTCTTTGTCTGGATGCATTATTATGTGTCAATGGATGCACTGCTTGGGGGATCTGAAAT | ||
| CTGGAGAGACATTGATTTTGCCCATGAAGCACCAGCTTTTCTGCCTTGGCATAGACTCTT | ||
| CTTGTTGCGGTGGGAACAAGAAATCCAGAAGCTGACAGGAGATGAAAACTTCACTATTCC | ||
| ATATTGGGACTGGCGGGATGCAGAAAAGTGTGACATTTGCACAGATGAGTACATGGGAGG | ||
| TCAGCACCCCACAAATCCTAACTTACTCAGCCCAGCATCATTCTTCTCCTCTTGGCAGAT | ||
| TGTCTGTAGCCGATTGGAGGAGTACAACAGCCATCAGTCTTTATGCAATGGAACGCCCGA | ||
| GGGACCTTTACGGCGTAATCCTGGAAACCATGACAAATCCAGAACCCCAAGGCTCCCCTC | ||
| TTCAGCTGATGTAGAATTTTGCCTGAGTTTGACCCAATATGAATCTGGTTCCATGGATAA | ||
| AGCTGCCAATTTCAGCTTTAGAAATACACTGGAAGGATTTGCTAGTCCACTTACTGGGAT | ||
| AGCGGATGCCTCTCAAAGCAGCATGCACAATGCCTTGCACATCTATATGAATGGAACAAT | ||
| GTCCCAGGTACAGGGATCTGCCAACGATCCTATCTTCCTTCTTCACCATGCATTTGTTGA | ||
| CAGTATTTTTGAGCAGTGGCTCCGAAGGCACCGTCCTCTTCAAGAAGTTTATCCAGAAGC | ||
| CAATGCACCCATTGGACATAACCGGGAATCCTACATGGTTCCTTTTATACCACTGTACAG | ||
| AAATGGTGATTTCTTTATTTCATCCAAAGATCTGGGCTATGACTATAGCTATCTACAAGA | ||
| TTCAGACCCAGACTCTTTTCAAGACTACATTAAGTCCTATTTGGAACAAGCGAGTCGGAT | ||
| CTGGTCATGGCTCCTTGGGGCGGCGATGGTAGGGGCCGTCCTCACTGCCCTGCTGGCAGG | ||
| GCTTGTGAGCTTGCTGTGTCGTCACAAGAGAAAGCAGCTTCCTGAAGAAAAGCAGCCACT | ||
| CCTCATGGAGAAAGAGGATTACCACAGCTTGTATCAGAGCCATTTATAAAAGGCTTAGGC | ||
| AATAGAGTAGGGCCAAAAAGCCTGACCTCACTCTAACTCAAAGTAATGTCCAGGTTCCCA | ||
| GAGAATATCTGCTGGTATTTTTCTGTAAAGACCATTTGCAAAATTGTAACCTAATACAAA | ||
| GTGTAGCCTTCTTCCAACTCAGGTAGAACACACCTGTCTTTGTCTTGCTGTTTTCACTCA | ||
| GCCCTTTTAACATTTTCCCCTAAGCCCATATGTCTAAGGAAAGGATGCTATTTGGTAATG | ||
| AGGAACTGTTATTTGTATGTGAATTAAAGTGCTCTTATTTTAAAAAATTGAAATAATTTT | ||
| GATTTTTGCCTTCTGATTATTTAAAGATCTATATATGTTTTATTGGCCCCTTCTTTATTT | ||
| TAATAAAACAGTGAGAAATCTA | ||
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| >XM_054369815.1 PREDICTED: Homo sapiens tyrosinase (TYR), transcript variant X1, mRNA | ||
| ACTGTAGTAGTAGCTGGAAAGAGAAATCTGTGACTCCAATTAGCCAGTTCCTGCAGACCT | ||
| TGTGAGGACTAGAGGAAGAATGCTCCTGGCTGTTTTGTACTGCCTGCTGTGGAGTTTCCA | ||
| GACCTCCGCTGGCCATTTCCCTAGAGCCTGTGTCTCCTCTAAGAACCTGATGGAGAAGGA | ||
| ATGCTGTCCACCGTGGAGCGGGGACAGGAGTCCCTGTGGCCAGCTTTCAGGCAGAGGTTC | ||
| CTGTCAGAATATCCTTCTGTCCAATGCACCACTTGGGCCTCAATTTCCCTTCACAGGGGT | ||
| GGATGACCGGGAGTCGTGGCCTTCCGTCTTTTATAATAGGACCTGCCAGTGCTCTGGCAA | ||
| CTTCATGGGATTCAACTGTGGAAACTGCAAGTTTGGCTTTTGGGGACCAAACTGCACAGA | ||
| GAGACGACTCTTGGTGAGAAGAAACATCTTCGATTTGAGTGCCCCAGAGAAGGACAAATT | ||
| TTTTGCCTACCTCACTTTAGCAAAGCATACCATCAGCTCAGACTATGTCATCCCCATAGG | ||
| GACCTATGGCCAAATGAAAAATGGATCAACACCCATGTTTAACGACATCAATATTTATGA | ||
| CCTCTTTGTCTGGATGCATTATTATGTGTCAATGGATGCACTGCTTGGGGGATATGAAAT | ||
| CTGGAGAGACATTGATTTTGCCCATGAAGCACCAGCTTTTCTGCCTTGGCATAGACTCTT | ||
| CTTGTTGCGGTGGGAACAAGAAATCCAGAAGCTGACAGGAGATGAAAACTTCACTATTCC | ||
| ATATTGGGACTGGCGGGATGCAGAAAAGTGTGACATTTGCACAGATGAGTACATGGGAGG | ||
| TCAGCACCCCACAAATCCTAACTTACTCAGCCCAGCATCATTCTTCTCCTCTTGGCAGAT | ||
| TGTCTGTAGCCGATTGGAGGAGTACAACAGCCATCAGTCTTTATGCAATGGAACGCCCGA | ||
| GGGACCTTTACGGCGTAATCCTGGAAACCATGACAAATCCAGAACCCCAAGGCTCCCCTC | ||
| TTCAGCTGATGTAGAATTTTGCCTGAGTTTGACCCAATATGAATCTGGTTCCATGGATAA | ||
| AGCTGCCAATTTCAGCTTTAGAAATACACTGGAAGGATTTGCTAGTCCACTTACTGGGAT | ||
| AGCGGATGCCTCTCAAAGCAGCATGCACAATGCCTTGCACATCTATATGAATGGAACAAT | ||
| GTCCCAGGTACAGGGATCTGCCAACGATCCTATCTTCCTTCTTCACCATGCATTTGTTGA | ||
| CAGTATTTTTGAGCAGTGGCTCCGAAGGCACCGTCCTCTTCAAGAAGTTTATCCAGAAGC | ||
| CAATGCACCCATTGGACATAACCGGGAATCCTACATGGTTCCTTTTATACCACTGTACAG | ||
| AAATGGTGATTTCTTTATTTCATCCAAAGATCTGGGCTATGACTATAGCTATCTACAAGA | ||
| TTCAGTGTCCCAATGGATACTTTTTACTACAAAGGCAACAAAATTTCCTGGATGAGCCAG | ||
| GGGAGAAGAGGCTCAATGAGTCATATTAGAAGCTTGAAGACCCAGACTCTTTTCAAGACT | ||
| ACATTAAGTCCTATTTGGAACAAGCGAGTCGGATCTGGTCATGGCTCCTTGGGGCGGCGA | ||
| TGGTAGGGGCCGTCCTCACTGCCCTGCTGGCAGGGCTTGTGAGCTTGCTGTGTCGTCACA | ||
| AGAGAAAGCAGCTTCCTGAAGAAAAGCAGCCACTCCTCATGGAGAAAGAGGATTACCACA | ||
| GCTTGTATCAGAGCCATTTATAAAAGGCTTAGGCAATAGAGTAGGGCCAAAAAGCCTGAC | ||
| CTCACTCTAACTCAAAGTAATGTCCAGGTTCCCAGAGAATATCTGCTGGTATTTTTCTGT | ||
| AAAGACCATTTGCAAAATTGTAACCTAATACAAAGTGTAGCCTTCTTCCAACTCAGGTAG | ||
| AACACACCTGTCTTTGTCTTGCTGTTTTCACTCAGCCCTTTTAACATTTTCCCCTAAGCC | ||
| CATATGTCTAAGGAAAGGATGCTATTTGGTAATGAGGAACTGTTATTTGTATGTGAATTA | ||
| AAGTGCTCTTATTTTAAAAAATTGAAATAATTTTGATTTTTGCCTTCTGATTATTTAAAG | ||
| ATCTATATATGTTTTATTGGCCCCTTCTTTATTTTAATAAAACAGTGAGAAATCTA |
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TRY gene, located at Chromosome 11.q23, is the gene associated with the most severe form of albinism caused by mutation in the tyrosinase gene . Variation in this gene can causes OCA type 1.