All diseases

OMIM ID
602522
OMIM term:
BARTTER SYNDROME, TYPE 4A
Alternative terms:

(∗) Location:
1p32.3   1p36.13  
(†) Associated OMIM genes:
BSND GENE   CLCNKB  
(‡) Associated MGI genes:
Bsnd  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/1ql9bkpn