All diseases

OMIM ID
268150
OMIM term:
RH-NULL, REGULATOR TYPE; RHN RH DEFICIENCY SYNDROME, INCLUDED
Alternative terms:

(∗) Location:
6p12.3  
(†) Associated OMIM genes:
RHAG  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/tefmmfb4