About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Mental Retardation, X-Linked, Syndromic 5; MRXS5
OMIM ID: 304340
Synonyms Mental Retardation, X-Linked 59; MRX59; Mental Retardation, X-Linked, Syndromic; Mental Retardation, X-Linked, Syndromic 21; MRXS21; Mental Retardation, X-Linked, Syndromic, Fried Type; MRXSF; Mental Retardation, X-Linked, with Dandy-Walker Malformation, Basal Ganglia Disease, and Seizures; Pettigrew Syndrome; PGS
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Ap1s2 AP1S2*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/08/2014
MGI 5.20
The Jackson Laboratory