All diseases

OMIM ID
600972
OMIM term:
ACHONDROGENESIS, TYPE IB; ACG1B
Alternative terms:

(∗) Location:
5q32  
(†) Associated OMIM genes:
SLC26A2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/rvon8ei8