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Summary ExpressionExpr. PhenotypesPheno. Gene Literature (18)Lit. (18) GO Terms (9)GO (9) Nucleotides (30)Nucl. (30) Proteins (26)Prot. (26) Interactants (161)Interact. (161) Wiki
XB-GENEPAGE-948282
???displayGene.symbol???:
 bsnd

???displayGene.name???: 
barttin CLCNK-type chloride channel accessory beta subunit

???displayGene.synonyms???
barttin ( Nomenclature history )

InterPro :
Barttin

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Diseases: 


Disease Ontology:
autosomal recessive nonsyndromic deafness [+]

MIM:
BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4A

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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