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Details of KDM5C gene in Homo sapiens
Disease |
|---|
| Disease |
OMIM id |
| Mental retardation, X-linked, syndromic, Claes-Jensen type (MRXSCJ) [MIM:300534]: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. MRXSCJ patients manifest mental retardation associated with variable features such as slowly progressive spastic paraplegia, seizures, facial dysmorphism. Note=The disease is caused by mutations affecting the gene represented in this entry. |
300534 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
| Kdm5c | lid | rbr-2 | Sp-Bbs2 |
