| Gene Symbol | Bsnd |
|---|---|
| Gene Name | Bartter syndrome, infantile, with sensorineural deafness (Barttin), transcript variant X2 |
| Entrez Gene ID | 101702314 |
For more information consult the page for NW_004624862.1 (Scaffold)
>XM_004869640.1 ATGGCAGACGAGAAGACCTTCCGCATTGGCTTCATCGTGCTGGGGCTCTTTCTGCTGTCCCTCGGCACCTTCCTAATGAGCCATGATCGGCCCCAGGTCTACGGCACCTTCTATGCCATGGGCAGCGTCATGGTGGTCGGGGGCGTCATCTGGAGCATGTGCCAGTGCTATCCTAAGGTCACCTTTGTGCCCGCTGACTCTGACTTCCAAGGCATCCTGTCTGCAAAGGCCCTGCTGGAGAATGGACTAGCTGCAGAGATGAAGAGCCCCCAGCCCCCCTACACCAGGCTGTGGGAGGAGGCCGCCTATGACCAGAGCCTGCCTGACTTCAGCCACATCCAGATGAAGGCCCTGGGCTACAGCGAGGACTCCCGCATGCTGCTGGCCTCTGAGCCAGGGCCAAGGCCCAGGGACACTGGAGAAGGTGGCCCTTGTGATGCTCAGGCCTGGGTGGAGGCGGCCGTGGTCGTCCACAGGGGCGTGGACCAGAGCGAGGGAGAAAGGACCCGGACTCAGAGCAGCCCCAGCCTGACGGGCTATCACCAGGGCCCTGCACCCTTGGCCTCCTTCCAAGATGACCTAGACATGGGCTCGAGTGAAGGCAGCAGCCCTGCCCCATCTCCACCTGGCAGAGCGGCGCCCTGGCCCCCACAGCAGGAGCCCAGGGCCAGCAGGAGCCCACTGGATGACTCCCATGACTTTGCTCTGATTGATGACCCCTCCACACCGGAGGGTGCACCCCGAGAGGGGCAGAGGCAGGAGGCAGTCCTGCTTGACAGCCGGCAGCGGTACCCGAGGAGGAAGGAGGAGGAGGAGAAAGCCTCGGACACAGGTGCAGGGGAGCCTGAGGAGGAAGAAGAGGACTTGTACTATGGGCTGCCCGACAGCCCTGGTGACTCCCTTCCGGACGAGGAAGTAGGCTTCGAGCCCGACGTCCAGGGCTGA
Bsnd PREDICTED: barttin isoform X2 [Heterocephalus glaber]
Length: 314 aa>XP_004869697.1 MADEKTFRIGFIVLGLFLLSLGTFLMSHDRPQVYGTFYAMGSVMVVGGVIWSMCQCYPKVTFVPADSDFQGILSAKALLENGLAAEMKSPQPPYTRLWEEAAYDQSLPDFSHIQMKALGYSEDSRMLLASEPGPRPRDTGEGGPCDAQAWVEAAVVVHRGVDQSEGERTRTQSSPSLTGYHQGPAPLASFQDDLDMGSSEGSSPAPSPPGRAAPWPPQQEPRASRSPLDDSHDFALIDDPSTPEGAPREGQRQEAVLLDSRQRYPRRKEEEEKASDTGAGEPEEEEEDLYYGLPDSPGDSLPDEEVGFEPDVQG