barttin CLCNK type accessory beta subunit [Source:MGI Symbol;Acc:MGI:2153465]
Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Chromosome 4: 106,340,653-106,349,480 reverse strand.
GRCm39:CM000997.3
This gene has 1 transcript (splice variant), 115 orthologues and is associated with 18 phenotypes.