| Entry |
|
| Symbol |
MEN1, MNN1
|
| Name |
|
| Pathway |
| map05202 | Transcriptional misregulation in cancer |
|
| Disease |
| H00045 | Pancreatic neuroendocrine tumor |
| H00246 | Primary hyperparathyroidism |
| H00247 | Multiple endocrine neoplasia syndrome |
| H01522 | Zollinger-Ellison syndrome |
| H02049 | Bilateral macronodular adrenal hyperplasia |
|
| 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
|
| 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 |
|
| Sequence |
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| LinkDB |
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