Intellectual Disability, X-linked, Syndromic, Houge Type(Mental retardation, x-linked, syndromic, Houge type) Explore Disorder's Alias
An X-linked recessive mode(s) within the Neurodevelopmental disorders category
Candidate Gene Information
An X-linked recessive mode(s) within the Neurodevelopmental disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | CNKSR2/22866 | connector enhancer of kinase suppressor of Ras 2 | Xp22.12 | ChrX, NC_000023.11 (21374418..21654689) |
280272 nt | 23 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
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Clinical Symptoms & Disabilities