| Gene Symbol | Dfna5 |
|---|---|
| Gene Name | deafness, autosomal dominant 5, transcript variant X2 |
| Entrez Gene ID | 101720023 |
For more information consult the page for NW_004624739.1 (Scaffold)
>XM_004839544.1 ATGTTTGCCAAAGCAACAAGGAATTTTCTTAAAGAAGTTGATGCTGGTGGTAACCTGATTTCAGTATCAAACTTGAATGATTCTGATAAGTTACAACCTCTAAGTCTGGTGACCAAAAGGAAGAGATACTGGTGCTGGCAGAGACCCAAGTACCAGTTTTTATCCGTCACCCTTGGAGATGTACTCACAGAGGACCAGTTTCTGAGTCCAGTGGTCGTGGAGTCAGACTTCGTGAAGTATGAGGGCAAGTTTGAAAACCACGTGAGTGGGACCATTGAGACCGTTCTGGGCAAGGTCAAGCTGAACGTGGGAGGCAAAGGCCTGGTGGAGAGCCAGTCTTCCTTTGGGACCCTGAGGAAGCAGGAGGTGGACTTGCAGCAGCTCATCAGAGACTCTGTGGAGAGAACAATAAACCTGAAAAACCCTGTGCTCCAGCAGGTGCTGGAGAGGAGGAAGGAGGTCCTGTGTGTCCTGACGCAGAAGATCGTGACGACCCAGAAGTGTGTGATATCGGAGCACGTTCAGATAGAGGAGAAGTGTGGCGGCATGGTGGGGATACAAACTAAGATAGTGCAGGTGTCGGCGATGGAGGACGGGAATGTCATCAAGGACACCAGTGTGGTGCTGGAGATCCCGGCTGCTACCACCATCGCCTATGGCATCATCGAGTTATATGTGAAACAGGATGGCCAGTTTGAATTCTGCCTCCTCCACGAGAAGCATGGTGGCTTTGAGCAGGAGCGGAGATCTGACCCTGTCTATCTGGACTACCTGGCCTGTCAGGAGTTTGGTTTCATGGATGTGCCAGATGCCAGGCATGGGACGTCTTCCCAGGATGGGCTGTTAAGTGTTTTAAATCAAGCAACTCTGCCACTGGAGAGGAATTTCCTTCCCTTCATGGAGCTGCCAGCAGGGCAGCAGACAGCTCTGTGCAACCTCTTGCAGGTGGTTCTGTTTGATGAGGAACTCCTGGTGGTCCTGGAGCAAGTGTGTGACGACATGGCTGGTGGCTTCTGGTCCCCACAGGCAGCGCTGGCAGTGGGGGAGCTGAAGCCCCCTCAGCAGCAGGACCTCATGGCCTTCCTGCAGCTGGTGGGATGCAGGATACAAGGGGAGTGTCCTGGCCCTGAGGATGAAGTCAGCAACCAGAAACTCTTTGCAACAGCCTACTTCCTGGTCAGTGCACTAGCAGAAATGCCAGATAATGCTGCAGCTCTGCTGGGCATTTGCTGTAAACTCCAGATCATTCCTACACTGTACCACTTGTCTGTTTAA
Dfna5 PREDICTED: non-syndromic hearing impairment protein 5 isoform X2 [Heterocephalus glaber]
Length: 424 aa>XP_004839601.1 MFAKATRNFLKEVDAGGNLISVSNLNDSDKLQPLSLVTKRKRYWCWQRPKYQFLSVTLGDVLTEDQFLSPVVVESDFVKYEGKFENHVSGTIETVLGKVKLNVGGKGLVESQSSFGTLRKQEVDLQQLIRDSVERTINLKNPVLQQVLERRKEVLCVLTQKIVTTQKCVISEHVQIEEKCGGMVGIQTKIVQVSAMEDGNVIKDTSVVLEIPAATTIAYGIIELYVKQDGQFEFCLLHEKHGGFEQERRSDPVYLDYLACQEFGFMDVPDARHGTSSQDGLLSVLNQATLPLERNFLPFMELPAGQQTALCNLLQVVLFDEELLVVLEQVCDDMAGGFWSPQAALAVGELKPPQQQDLMAFLQLVGCRIQGECPGPEDEVSNQKLFATAYFLVSALAEMPDNAAALLGICCKLQIIPTLYHLSV