Entry |
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Symbol |
MEN1, MNN1
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Name |
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Pathway |
map05202 | Transcriptional misregulation in cancer |
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Disease |
H00045 | Pancreatic neuroendocrine tumor |
H00246 | Primary hyperparathyroidism |
H00247 | Multiple endocrine neoplasia syndrome |
H01522 | Zollinger-Ellison syndrome |
H02049 | Bilateral macronodular adrenal hyperplasia |
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Brite |
KEGG Orthology (KO) [BR:ko00001]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
K14970 MEN1, MNN1; menin
09167 Endocrine and metabolic disease
04934 Cushing syndrome
K14970 MEN1, MNN1; menin
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins
K14970 MEN1, MNN1; menin
Chromosome and associated proteins [BR:ko03036]
Eukaryotic type
Histone modification proteins
HMT complexes
MLL-HCF complex
K14970 MEN1, MNN1; menin
|
Genes |
» show all
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Reference |
|
Authors |
Wu X, Hua X |
Title |
Menin, histone h3 methyltransferases, and regulation of cell proliferation: current knowledge and perspective. |
Journal |
|
Reference |
|
Authors |
Kaji H, Canaff L, Lebrun JJ, Goltzman D, Hendy GN |
Title |
Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling. |
Journal |
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Sequence |
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LinkDB |
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