Bos taurus Gene: BSND
Summary
InnateDB Gene IDBG-639028.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BSND
Gene Name barttin
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000013241
Encoded Proteins
Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000162399:
This gene encodes an essential beta subunit for CLC chloride channels. These heteromeric channels localize to basolateral membranes of renal tubules and of potassium-secreting epithelia of the inner ear. Mutations in this gene have been associated with Bartter syndrome with sensorineural deafness. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 3:91901853-91911965
Strand Reverse strand
Band
Transcripts
ENSBTAT00000017615 ENSBTAP00000017615
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
Predicted by orthology
Total 3 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005254 chloride channel activity
GO:0005515 protein binding
Biological Process
GO:0006821 chloride transport
GO:1902476 chloride transmembrane transport
Cellular Component
GO:0005887 integral component of plasma membrane
GO:0016323 basolateral plasma membrane
GO:0043234 protein complex
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Stimuli-sensing channels pathway
Transmembrane transport of small molecules pathway
Ion channel transport pathway
Stimuli-sensing channels pathway
Ion channel transport pathway
Transmembrane transport of small molecules pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Bt.44214
RefSeq NM_001193084 XM_005204605
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas