BSND gene homepage

General information
Gene symbol BSND
Gene name Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Chromosome 1
Chromosomal band p32.3
Imprinted Unknown
Genomic reference NG_008965.1
Transcript reference NM_057176.2
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 65
Unique public DNA variants reported 65
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 16512
Entrez Gene 7809
PubMed articles BSND
OMIM - Gene 606412


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001706 1 Bartter syndrome, infantile, with sensorineural deafness (Barttin) NM_057176.2 NP_476517.1 65