multiple endocrine neoplasia type 1

Summary
Synonym
  • MEN type I
  • Wermer syndrome
  • Wermer's syndrome
Definition
A multiple endocrine neoplasia that has_material_basis_in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas.
Super Class
autosomal dominant disease multiple endocrine neoplasia
External Links
Disease Ontology
DOID:10017
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 22 in total
Gene ID Gene Symbol Description Source
28 ABO ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
353 APRT adenine phosphoribosyltransferase
1591 CYP24A1 cytochrome P450 family 24 subfamily A member 1
2526 FUT4 fucosyltransferase 4
2597 GAPDH glyceraldehyde-3-phosphate dehydrogenase
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5331 PLCB3 phospholipase C beta 3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024