Target intelligence / Profile preview

VANGL planar cell polarity protein 1 (VANGL1)

Target
VANGL1
Molecular classification
Planar cell polarity core protein, Tetraspanin family protein, Transmembrane protein, Membrane-associated signaling molecule
01

Overview

VANGL planar cell polarity protein 1 (VANGL1) is a core component of the planar cell polarity (PCP) pathway, essential for regulating coordinated orientation and alignment of cells across epithelial tissues perpendicular to the apical-basal axis[7]. It is a tetraspanin (four-pass transmembrane) protein localized at the cell membrane and oligomerizes as dimers of trimers, interacting principally with the PCP effector Prickle1 (PK1)[2][4][7]. VANGL1 is critical for tissue morphogenesis, neural tube closure, and collective cell migration, especially during embryogenesis[2][3][4][5][6][7]. Disease-associated mutations disrupt its interactions and/or oligomerization, leading to defects such as neural tube defects and increasing susceptibility to certain cancers[2][5][7]. Although currently not the direct pharmacological target of approved therapeutics or a validated biomarker for drug efficacy, its mutation status is clinically relevant for risk prediction in congenital malformations and some cancers[5][6][7].

Other names
Vang-like protein 1STB2LPP2Loop-tail protein 2 homologStrabismus 2Van Gogh-like protein 1KITENINSTBM2vang-like protein 1KAI1 C-terminal interacting tetraspaninloop-tail protein 2 homologstrabismus 2van Gogh-like protein 1vang-like 1 (van gogh, Drosophila)VANGL1
02

Mechanism of action

Currently, no approved drugs are documented as targeting VANGL1 directly; thus, mechanisms of action for pharmacological agents cannot be specified

03

Biological functions

Planar cell polarity (PCP) signalingCell orientation and tissue morphogenesisEpithelial cell polarityRegulation of collective cell behaviorEmbryonic development (especially neural tube closure)Wound healing in intestinal mucosa
04

Disease associations

Neural tube defects (e.g., spina bifida, sacral defect with anterior meningocele)Cancer (including hepatocellular carcinoma and potentially other tumor types)
05

Safety considerations

Loss-of-function mutations can cause developmental defects (notably neural tube defects), raising concerns for potential toxicity if targeted in therapeutic contexts
06

Biomarkers

Disease-associated point mutations in VANGL1 are biomarkers for risk of neural tube defects and certain cancers

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