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familial adenomatous polyposis 1
Summary
- Definition
- A familial adenomatous polyposis that has_material_basis_in heterozygous mutation in the APC gene on chromosome 5q22.
- Super Class
- autosomal dominant disease familial adenomatous polyposis
External Links
- Disease Ontology
- DOID:0080409
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 8658 | TNKS | tankyrase | |
| 9536 | PTGES | prostaglandin E synthase | |
| 22914 | KLRK1 | killer cell lectin like receptor K1 | |
| 22934 | RPIA | ribose 5-phosphate isomerase A | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 27306 | HPGDS | hematopoietic prostaglandin D synthase | |
| 54659 | UGT1A3 | UDP glucuronosyltransferase family 1 member A3 | |
| 79695 | GALNT12 | polypeptide N-acetylgalactosaminyltransferase 12 | |
| 151056 | PLB1 | phospholipase B1 | |
| 192134 | B3GNT6 | UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 |
Related Glycoprotein
