Bsnd - barttin CLCNK type accessory subunit beta Gene

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 192675

Summary

Enables Chloride Channel regulator activity. Involved in chloride transport. Predicted to be part of protein-containing complex. Predicted to be active in basolateral plasma membrane. Predicted to be integral component of plasma membrane. Human ortholog(s) of this gene implicated in Bartter disease; Bartter disease type 4a; and sensorineural hearing loss. Orthologous to human BSND (barttin CLCNK type accessory subunit beta). [provided by Alliance of Genome Resources, Apr 2022]

Bsnd Products (1)

mRNA Protein Name
NM_138979.2 NP_620435.1 barttin

Gene Ontology

  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence References Source
enables chloride channel regulator activity IMP
IMP: Inferred from mutant phenotype
12111250 RGD
Biological Process GO Annotation Evidence References Source
involved in chloride transport IMP
IMP: Inferred from mutant phenotype
12111250 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

barttin

  • Bartter syndrome, infantile, with sensorineural deafness (Barttin)

  • barttin CLCNK type accessory beta subunit

  • barttin CLCNK-type chloride channel accessory beta subunit

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS01645 BSND Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Bsnd NCBI NCBI:7809