Peutz-Jeghers Syndrome(Hamartomatous intestinal polyposis) Explore Disorder's Alias
An Autosomal dominant mode(s) within the Gastrointestinal disorders category
Candidate Gene Information
An Autosomal dominant mode(s) within the Gastrointestinal 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 | STK11/6794 | serine/threonine kinase 11 | 19p13.3 | Chr19, NC_000019.10 (1205778..1228431) |
22654 nt | 12 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |