About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease

Term: Mental Retardation, X-Linked, with or without Seizures, Arx-Related;
OMIM ID: 300419

Synonyms Mental Retardation, X-Linked 29; MRX29; Mental Retardation, X-Linked 32; MRX32; Mental Retardation, X-Linked 33; MRX33; Mental Retardation, X-Linked 38; MRX38; Mental Retardation, X-Linked 43; MRX43; Mental Retardation, X-Linked 54; MRX54; Mental Retardation, X-Linked 76; MRX76; Mental Retardation, X-Linked 87; MRX87; Mrxarx
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Arx ARX
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
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
04/03/2013
MGI 5.12 		The Jackson Laboratory