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NTRK3 mutated L686M

Function

Receptor tyrosine kinase involved in nervous system and probably heart development. Upon binding of its ligand NTF3/neurotrophin-3, NTRK3 autophosphorylates and activates different signaling pathways, including the phosphatidylinositol 3-kinase/AKT and the MAPK pathways, that control cell survival and differentiation.

Involvement in disease

Defects in NTRK3 are associated with susceptibility to congenital heart defects (CHD). A disease characterized by congenital developmental abnormalities involving structures of the heart. CHD are the most common major birth defects and the leading cause of death from congenital malformations.

Post-translational modifications

Ligand-mediated auto-phosphorylation.

Sequence similarities

Belongs to the protein kinase superfamily. Tyr protein kinase family. Insulin receptor subfamily.

Tissue specificity

Widely expressed but mainly in nervous tissue. Isoform 2 is expressed at higher levels in adult brain than in fetal brain.

Cellular localization

  • Membrane
  • Single-pass type I membrane protein

Alternative names

TRKC, NTRK3, NT-3 growth factor receptor, GP145-TrkC, Neurotrophic tyrosine kinase receptor type 3, TrkC tyrosine kinase, Trk-C

Target type

Proteins

Primary research area

Oncology

Other research areas

  • Immuno-oncology
  • Neuroscience

Molecular weight

94428Da

We found 1 product in 1 category

Proteins & Peptides

Target

Species of origin

Search our catalogue for 'NTRK3 mutated L686M' (1)

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