Sequence details NCBI ID: XM_004869639.1 (Coding sequence)

Details from NCBI annotation

Gene Symbol Bsnd
Gene Name Bartter syndrome, infantile, with sensorineural deafness (Barttin), transcript variant X1
Entrez Gene ID 101702314

Database interlinks

Part of NW_004624862.1 (Scaffold)

For more information consult the page for NW_004624862.1 (Scaffold)

Genome Location

Sequence Coding sequence

Length: 945 bp    Location: 4927120..4917630   Strand: -
Raw sequence   
>XM_004869639.1
ATGGCAGACGAGAAGACCTTCCGCATTGGCTTCATCGTGCTGGGGCTCTTTCTGCTGTCCCTCGGCACCTTCCTAATGAGCCATGATCGGCCCCAGGTCTACGGCACCTTCTATGCCATGGGCAGCGTCATGGTGGTCGGGGGCGTCATCTGGAGCATGTGCCAGTGCTATCCTAAGGTCACCTTTGTGCCCGCTGACTCTGACTTCCAAGGCATCCTGTCTGCAAAGGCCCTGCTGGAGAATGGACTAGCTGCAGAGATGAAGAGCCCCCAGCCCCCCTACACCAGGCTGTGGGAGGAGGCCGCCTATGACCAGAGCCTGCCTGACTTCAGCCACATCCAGATGAAGGCCCTGGGCTACAGCGAGGACTCCCGCATGCTGCTGGCCTCTGAGCCAGGGCCAAGGCCCAGGGACACTGGAGAAGGTGGCCCTTGTGATGCTCAGGCCTGGGTGGAGGCGGCCGTGGTCGTCCACAGGGGCGTGGACCAGAGCGAGGGAGAAAGGACCCGGACTCAGAGCAGCCCCAGCCTGACGGGCTATCACCAGGGCCCTGCACCCTTGGCCTCCTTCCAAGATGACCTAGACATGGGCTCGAGTGAAGGCAGCAGCCCTGCCCCATCTCCACCTGGCAGAGCGGCGCCCTGGCCCCCACAGCAGGAGCCCAGGGCCAGCAGGAGCCCACTGGATGACTCCCATGACTTTGCTCTGATTGATGACCCCTCCACACCGGAGGGTGCACCCCGAGAGGGGCAGAGGCAGGAGGCAGTCCTGCTTGACAGCCGGCAGCGGTACCCGAGGAGGAAGGAGGAGGAGGAGAAAGCCTCGGACACAGGTGCAGGGGAGCCTGAGGAGGAAGAAGAGGACTTGTACTATGGGCTGCCCGACAGCCCTGGTGACTCCCTTCCGGACGAGGAAGTAGGCTTCGAGCCCGACGTCCAGGGCTGA

Related Sequences

XP_004869696.1 Protein

Bsnd PREDICTED: barttin isoform X1 [Heterocephalus glaber]

Length: 314 aa      
>XP_004869696.1
MADEKTFRIGFIVLGLFLLSLGTFLMSHDRPQVYGTFYAMGSVMVVGGVIWSMCQCYPKVTFVPADSDFQGILSAKALLENGLAAEMKSPQPPYTRLWEEAAYDQSLPDFSHIQMKALGYSEDSRMLLASEPGPRPRDTGEGGPCDAQAWVEAAVVVHRGVDQSEGERTRTQSSPSLTGYHQGPAPLASFQDDLDMGSSEGSSPAPSPPGRAAPWPPQQEPRASRSPLDDSHDFALIDDPSTPEGAPREGQRQEAVLLDSRQRYPRRKEEEEKASDTGAGEPEEEEEDLYYGLPDSPGDSLPDEEVGFEPDVQG