Human Disease and Mouse Model Detail

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Human Disease

Term: Partington X-Linked Mental Retardation Syndrome; PRTS
OMIM ID: 309510

Synonyms

Mental Retardation, X-Linked 36; MRX36; Mental Retardation, X-Linked, Syndromic 1; MRXS1; Mental Retardation, X-Linked, with Dystonic Movements, Ataxia, and Seizures; Partington Syndrome

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

...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
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