Gene

bsnd

ID
ZDB-GENE-070705-548
Name
barttin CLCNK type accessory subunit beta
Symbol
bsnd Nomenclature History
Previous Names
  • im:7136367
  • si:dkeyp-51f12.4
Type
protein_coding_gene
Location
Chr: 20 Mapping Details/Browsers
Description
Predicted to have chloride channel regulator activity. Predicted to be involved in chloride transport. Predicted to localize to basolateral plasma membrane and integral component of plasma membrane. Human ortholog(s) of this gene implicated in Bartter disease; Bartter disease type 4a; and sensorineural hearing loss. Is expressed in pronephric duct. Orthologous to human BSND (barttin CLCNK type accessory subunit beta).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
6 figures from 4 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With bsnd Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Bartter disease type 4a Alliance Bartter syndrome, type 4a 602522
Bartter disease type 4a Alliance Sensorineural deafness with mild renal dysfunction 602522
Associated With bsnd Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR029181 Barttin
Domain Details Per Protein
Protein Length Barttin
UniProtKB:E7F4W6 175
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA bsnd-201 (1) Havana 886 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations