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Gene Symbol |
NGF |
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Aliases |
Beta-NGF, HSAN5, NGFB |
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Entrez Gene ID |
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Gene Name |
Nerve growth factor |
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Chromosomal Location |
1p13.2 |
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HGNC ID |
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Summary |
This gene is a member of the NGF-beta family and encodes a secreted protein which homodimerizes and is incorporated into a larger complex. This protein has nerve growth stimulating activity and the complex is involved in the regulation of growth and the differentiation of sympathetic and certain sensory neurons. Mutations in this gene have been associated with hereditary sensory and autonomic neuropathy, type 5 (HSAN5), and dysregulation of this gene's expression is associated with allergic rhinitis. [provided by RefSeq, Jul 2008]
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RefSeq DNA |
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RefSeq mRNA |
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e!Ensembl
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Protein Information |
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Protein Name |
Beta-nerve growth factor, nerve growth factor (beta polypeptide), nerve growth factor, beta subunit, pro-nerve growth factor long |
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Function |
Nerve growth factor is important for the development and maintenance of the sympathetic and sensory nervous systems. Extracellular ligand for the NTRK1 and NGFR receptors, activates cellular signaling cascades to regulate neuronal proliferation, differentiation and survival. The immature NGF precursor (proNGF) functions as ligand for the heterodimeric receptor formed by SORCS2 and NGFR, and activates cellular signaling cascades that lead to inactivation of RAC1 and/or RAC2, reorganization of the actin cytoskeleton and neuronal growth cone collapse. In contrast to mature NGF, the precursor form (proNGF) promotes neuronal apoptosis (in vitro) (By similarity). Inhibits metalloproteinase-dependent proteolysis of platelet glycoprotein VI. Binds lysophosphatidylinositol and lysophosphatidylserine between the two chains of the homodimer. The lipid-bound form promotes histamine relase from mast cells, contrary to the lipid-free form |
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UniProt |
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PDB |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000215754 |
P14174 |
P14174 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Atonic seizures |
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Endocrine System Diseases |
PCOS |
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Eye Diseases |
Corneal ulcer |
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Neoplasms |
Lung Cancer |
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Nervous System Diseases |
Cerebral Artery Infarction |
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Neuropathy |
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Parkinson Disease |
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Status Epilepticus |
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Seizures |
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Degenerative Diseases Central Nervous System |
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Jacksonian Seizure |
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Petit mal status |
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Epilepsy |
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Ramsay Hunt Paralysis Syndrome |
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Dysautonomia |
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Middle Cerebral Artery Syndrome |
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Cerebral Thrombosis |
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Brain Infarction |
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Psychiatric/Brain disorders |
Amnesia |
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Pain Disorder |
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Lewy Body Disease |
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Mental Depression |
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Renal Disorder |
Nephritis |
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Overactive Bladder |
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Nephritis, Interstitial |
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Glomerulonephritis |
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Kidney Failure |
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Kidney Insufficiency |
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Reproductive disorders |
Cystitis |
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Respiratory Tract Diseases |
Chronic Lung Injury |
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Bronchial hyperreactivity |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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17alpha-hydroxylase gene |
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Related
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These results suggest that overproduction of ovarian NGF is a component of polycystic ovarian morphology in both humans and rodents and that a persistent elevation in plasma LH levels is required for the morphological abnormalities to appear. |
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