Menin Products

Description

Multiple Endocrine Neoplasia is an autosomal dominant disorder characterized by a high frequency of peptic ulcer disease and primary endocrine abnormalities involving the pituitary, parathyroid, and pancreas.

Bioinformatics

Entrez	4221 Human 17283 Mouse 29417 Rat
Uniprot	AAH02544 Human AAH02544.1 Human NP_570711 Human NP_000235 Human NP_000235.2 Human O00255 Human
Product By Gene ID	4221
Alternate Names	menin multiple multiple endocrine neoplasia I

Diseases related to Menin

Discover more about diseases related to Menin.

Multiple Endocrine Neoplasia Type 1
Neoplasms
Multiple Endocrine Neoplasia
Endocrine Gland Neoplasms
Pituitary Diseases
Adenoma
Malignant Neoplasms
Pancreatic Neoplasm
Cell Transformation, Neoplastic
Pituitary Neoplasms
Hyperparathyroidism, Primary
Parathyroid Neoplasms
Carcinoma
Neuroendocrine Tumors
Hyperplasia
Malignant Paraganglionic Neoplasm
Insulinoma
Carcinoid Tumor
Pituitary Adenoma

Pathways for Menin

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Pathogenesis
Localization
Angiogenesis
Cell Proliferation
Secretion
Cell Cycle
Methylation
Cell Growth
Translation
Oncogenesis
Cell Differentiation
Hormone Secretion
S Phase
Osteoblast Differentiation
Dna Methylation
Gene Silencing
Enucleation
Metaphase
Regulation Of Cell Proliferation
Rna Interference

Research Areas for Menin

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Cancer
DNA Repair
Transcription Factors and Regulators
Tumor Suppressors

PTMs for Menin

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Methylation
Phosphorylation
Cleavage
Acetylation
Reduction
Hydroxylation
Deacetylation
Oxidation
Myristoylation

Bioinformatics Tool for Menin

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