The following gene names and symbols are associated with antigen Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) across different species:

Bartter syndrome, infantile, with sensorineural deafness (Barttin) (Bsnd), Bartter syndrome, infantile, with sensorineural deafness (Barttin) (BSND)

Other aliases include:

MGC47291, MGC93168, BSND, DKFZp469H092

On the protein level the following designations are being used for antigen Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin):

Bartter syndrome, infantile, with sensorineural deafness (Barttin) – barttin – OTTMUSP00000008552

Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) fulfills a number of functions:

chloride channel activity – protein binding – chloride channel regulator activity

Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) is relevant to the following processes:

cellular chloride ion homeostasis – cellular ion homeostasis – cellular potassium ion homeostasis – sensory perception of sound – chloride transport

Locations for Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin):

basolateral plasma membrane – integral to membrane – integral to plasma membrane – membrane – plasma membrane – protein complex – cellular_component

Source: NCBI Entrez Gene, Gene Ontology