Details from NCBI annotation

Gene Symbol Bsnd
Gene Name Bartter syndrome, infantile, with sensorineural deafness (Barttin), transcript variant X5
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: 879 bp    Location: 4927120..4917630   Strand: -
>XM_004869643.1
ATGGCAGACGAGAAGACCTTCCGCATTGGCTTCATCGTGCTGGGGCTCTTTCTGCTGTCCCTCGGCACCTTCCTAATGAGCCATGATCGGCCCCAGGTCTACGGCACCTTCTATGCCATGGGCAGCGTCATGGTGGTCGGGGGCGTCATCTGGAGCATGTGCCAGTGCTATCCTAAGGTCACCTTTGTGCCCGCTGACTCTGACTTCCAAGGCATCCTGTCTGCAAAGGCCCTGCTGGAGAATGGACTAGCTGCAGAGATGAAGAGCCACATCCAGATGAAGGCCCTGGGCTACAGCGAGGACTCCCGCATGCTGCTGGCCTCTGAGCCAGGGCCAAGGCCCAGGGACACTGGAGAAGGTGGCCCTTGTGATGCTCAGGCCTGGGTGGAGGCGGCCGTGGTCGTCCACAGGGGCGTGGACCAGAGCGAGGGAGAAAGGACCCGGACTCAGAGCAGCCCCAGCCTGACGGGCTATCACCAGGGCCCTGCACCCTTGGCCTCCTTCCAAGATGACCTAGACATGGGCTCGAGTGAAGGCAGCAGCCCTGCCCCATCTCCACCTGGCAGAGCGGCGCCCTGGCCCCCACAGCAGGAGCCCAGGGCCAGCAGGAGCCCACTGGATGACTCCCATGACTTTGCTCTGATTGATGACCCCTCCACACCGGAGGGTGCACCCCGAGAGGGGCAGAGGCAGGAGGCAGTCCTGCTTGACAGCCGGCAGCGGTACCCGAGGAGGAAGGAGGAGGAGGAGAAAGCCTCGGACACAGGTGCAGGGGAGCCTGAGGAGGAAGAAGAGGACTTGTACTATGGGCTGCCCGACAGCCCTGGTGACTCCCTTCCGGACGAGGAAGTAGGCTTCGAGCCCGACGTCCAGGGCTGA

Related Sequences

XP_004869700.1 Protein

Bsnd PREDICTED: barttin isoform X5 [Heterocephalus glaber]

Length: 292 aa     
>XP_004869700.1
MADEKTFRIGFIVLGLFLLSLGTFLMSHDRPQVYGTFYAMGSVMVVGGVIWSMCQCYPKVTFVPADSDFQGILSAKALLENGLAAEMKSHIQMKALGYSEDSRMLLASEPGPRPRDTGEGGPCDAQAWVEAAVVVHRGVDQSEGERTRTQSSPSLTGYHQGPAPLASFQDDLDMGSSEGSSPAPSPPGRAAPWPPQQEPRASRSPLDDSHDFALIDDPSTPEGAPREGQRQEAVLLDSRQRYPRRKEEEEKASDTGAGEPEEEEEDLYYGLPDSPGDSLPDEEVGFEPDVQG