GDNF

glial cell derived neurotrophic factor

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. The recombinant form of this protein, a highly conserved neurotrophic factor, was shown to promote the survival and differentiation of dopaminergic neurons in culture, and was able to prevent apoptosis of motor neurons induced by axotomy. This protein is a ligand for the product of the RET (rearranged during transfection) protooncogene. Mutations in this gene may be associated with Hirschsprung disease and Tourette syndrome. This gene encodes multiple protein isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Aug 2016]

From UniProt:

Neurotrophic factor that enhances survival and morphological differentiation of dopaminergic neurons and increases their high-affinity dopamine uptake.

Covered on Genetics Home Reference:

From NCBI Gene:

  • Hirschsprung disease 3
  • Pheochromocytoma
  • Congenital central hypoventilation

From UniProt:

Hirschsprung disease 3 (HSCR3): A disorder of neural crest development characterized by absence of enteric ganglia along a variable length of the intestine. It is the most common cause of congenital intestinal obstruction. Early symptoms range from complete acute neonatal obstruction, characterized by vomiting, abdominal distention and failure to pass stool, to chronic constipation in the older child. [MIM:613711]

Congenital central hypoventilation syndrome (CCHS): Rare disorder characterized by abnormal control of respiration in the absence of neuromuscular or lung disease, or an identifiable brain stem lesion. A deficiency in autonomic control of respiration results in inadequate or negligible ventilatory and arousal responses to hypercapnia and hypoxemia. [MIM:209880]

Cytogenetic Location: 5p13.1-p12, which is the short (p) arm of chromosome 5 between positions 13.1 and 12

Molecular Location: base pairs 37,812,677 to 37,840,044 on chromosome 5 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 5p13.1-p12, which is the short (p) arm of chromosome 5 between positions 13.1 and 12
  • ATF
  • ATF1
  • ATF2
  • HFB1-GDNF
  • HSCR3