Velopharyngeal Insufficiency Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Inability of velopharyngeal sphincter to sufficiently separate the nasal cavity from the oral cavity during speech. (Human Phenotype Ontology, HP_0000220)
External Link https://www.disgenet.org/browser/0/1/0/C0042454
Similar Terms
Downloads & Tools

Genes

27 genes associated with the disease Velopharyngeal Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARHGAP29 Rho GTPase activating protein 29
BMP4 bone morphogenetic protein 4
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
COL2A1 collagen, type II, alpha 1
COMT catechol-O-methyltransferase
DGCR2 DiGeorge syndrome critical region gene 2
DGCR6 DiGeorge syndrome critical region gene 6
DGCR8 DGCR8 microprocessor complex subunit
DLG1 discs, large homolog 1 (Drosophila)
DLX4 distal-less homeobox 4
ESS2 ess-2 splicing factor homolog
GRHL3 grainyhead-like 3 (Drosophila)
IRF6 interferon regulatory factor 6
LAMA1 laminin, alpha 1
MSX1 msh homeobox 1
NECTIN1 nectin cell adhesion molecule 1
NEK1 NIMA-related kinase 1
OTX2 orthodenticle homeobox 2
RAI1 retinoic acid induced 1
RLIM ring finger protein, LIM domain interacting
SELENON selenoprotein N
SF3B4 splicing factor 3b, subunit 4, 49kDa
TBX1 T-box 1
TP63 tumor protein p63
TSPAN10 tetraspanin 10
TUBB6 tubulin, beta 6 class V
UBB ubiquitin B