Description
Bartter syndrome, infantile, with sensorineural deafness (Barttin) [Source:HGNC Symbol;Acc:16512]
Gene Synonyms
BART, DFNB73
Location
Chromosome 1: 55,464,606-55,476,556 forward strand.
GRCh37:CM000663.1
About this gene
This gene has 1 transcript (splice variant) and is associated with 5 phenotypes.
Transcripts
