Bartter syndrome, infantile, with sensorineural deafness (Barttin) Gene Detail


Symbol:
Name:
ID:
BSND
Bartter syndrome, infantile, with sensorineural deafness (Barttin)
GC:00358
Aliases & Descriptions for BSND gene
Gene name: BSND
Chromosome: 1p32.3
Previous Symbols: DFNB73
Previous Names: deafness, autosomal recessive 73
Aliases: BART
Name Aliases:
product Type: gene with protein/antibody/ELISA product

Bartter syndrome, infantile, with sensorineural deafness (Barttin) database Links


Mouse Genome Database ID: MGI:2153465 Rat Genome Database ID: RGD:621139
According to HGNC, Entrez Gene, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, OMIM, GeneLoc , and/or Ensembl, miRBase
HGNC ID: HGNC:16512 RefSeq IDs: NM_057176
Entrez Gene ID: 7809 Ensembl Gene ID: ENSG00000162399
VEGA IDs: OTTHUMG00000008112 UniProt ID: Q8WZ55
UCSC ID: uc001cye.2 OMIM ID: 606412
Pubmed: PMID11687798 PMID 11734858 PMID 19646679
CCDS IDs: CCDSCCDS602.1

Products for BSND gene

(SPECIES:Human;Rat;Mouse and other species fluids)

Catalog Product Name Application Brand Products with us for BSND gene
GCE00358 Bartter syndrome, infantile, with sensorineural deafness (Barttin) ELISA kit ELISA n/a
GCPA00358 Bartter syndrome, infantile, with sensorineural deafness (Barttin) Polyconal Antibody Polyconal Antibody n/a
GCMA00358 Bartter syndrome, infantile, with sensorineural deafness (Barttin) Monaconal Antibody Monaconal Antibody n/a
GCP00358 Bartter syndrome, infantile, with sensorineural deafness (Barttin) Protein Protein n/a
BSND BSND - related Gene