Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | BSND | contributors: mct/npt - updated : 12-01-2007 |
HGNC name | Bartter syndrome, infantile, with sensorineural deafness (Barttin) |
HGNC id | 16512 |
|
ASSOCIATED DISORDERS |
corresponding disease(s) | BSND4 , DFNB73 |
Susceptibility |
Variant & Polymorphism
| |
Candidate gene
Marker
| Therapy target
|
| |
ANIMAL & CELL MODELS |