All diseases

OMIM ID
149400
OMIM term:
HYPEREKPLEXIA, HEREDITARY 1; HKPX1
Alternative terms:
STARTLE DISEASE, FAMILIAL
STARTLE REACTION, EXAGGERATED
EXAGGERATED STARTLE REACTION
STHE
STIFF-BABY SYNDROME
STIFF-MAN SYNDROME, CONGENITAL
STIFF-PERSON SYNDROME, CONGENITAL
KOK DISEASE
(∗) Location:
5q33.1  
(†) Associated OMIM genes:
GLRA1  
(‡) Associated MGI genes:
Glra1  

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* quick link - http://q.sanger.ac.uk/ma0mpdc8