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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Carney complex
Summary
- Synonym
-
- Carney Complex, Type 1
- Carney Complex, Type 2
- Carney Syndrome
- Carney complex variant
- LAMB Syndrome
- NAME Syndrome
- Definition
- A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity.
- Super Class
- autosomal dominant disease syndrome
External Links
- Disease Ontology
- DOID:0050471
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 353 | APRT | adenine phosphoribosyltransferase | |
| 847 | CAT | catalase | |
| 1555 | CYP2B6 | cytochrome P450 family 2 subfamily B member 6 | |
| 1588 | CYP19A1 | cytochrome P450 family 19 subfamily A member 1 | |
| 5728 | PTEN | phosphatase and tensin homolog | |
| 6391 | SDHC | succinate dehydrogenase complex subunit C | |
| 54658 | UGT1A1 | UDP glucuronosyltransferase family 1 member A1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P04040 | Catalase | |
| P07741 | Adenine phosphoribosyltransferase | |
| P22309 | UDP-glucuronosyltransferase 1A1 | |
| P60484 | Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN |
