Obsessive Compulsive Disorder
An Autosomal dominant mode(s) within the Neurodevelopmental disorders category
Candidate Gene Information
An Autosomal dominant 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 | HTR2A/3356 | 5-hydroxytryptamine receptor 2A | 13q14.2 | Chr13, NC_000013.11 (46831546..46898082, complement) |
66537 nt | 5 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | SLC6A4/6532 | solute carrier family 6 member 4 | 17q11.2 | Chr17, NC_000017.11 (30194319..30235697, complement) |
41379 nt | 15 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 3 | HTR2C/3358 | 5-hydroxytryptamine receptor 2C | Xq23 | ChrX, NC_000023.11 (114584086..114910061) |
325976 nt | 7 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: GTR MalaCards NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |