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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 23/10/2006 |
Symbol | MRX28 |
Location | Xq28 |
HGNC id | 7258 |
Name | mental retardation, 28 |
Corresponding gene | MECP2 |
Main clinical features | nonspecific X-linked mental retardation |
Genetic determination | sex linked |
Function/system disorder | mental retardation |
Type | disease |
Gene product |
Name | methyl-CPG binding protein 2 |
Remark(s) |
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