All diseases

OMIM ID
161800
OMIM term:
NEMALINE MYOPATHY 3; NEM3 MYOPATHY, ACTIN, CONGENITAL, WITH EXCESS OF THIN MYOFILAMENTS, INCLUDED
Alternative terms:
NEMALINE MYOPATHY 3, WITH INTRANUCLEAR RODS, INCLUDED
MYOPATHY, ACTIN, CONGENITAL, WITH CORES, INCLUDED
(∗) Location:
1q42.13  
(†) Associated OMIM genes:
ACTA1  
(‡) Associated MGI genes:
Acta1  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/5w9y5gwd