Abnormality Of The Pharynx Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An anomaly of the pharynx, i.e., of the tubular structure extending from the base of the skull superiorly to the esophageal inlet inferiorly. (Human Phenotype Ontology, HP_0000600)
External Link https://www.disgenet.org/browser/0/1/0/C4025838
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Genes

22 genes associated with the disease Abnormality Of The Pharynx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
COMT catechol-O-methyltransferase
CTC1 CTS telomere maintenance complex component 1
DKC1 dyskeratosis congenita 1, dyskerin
GP1BB glycoprotein Ib (platelet), beta polypeptide
HIRA histone cell cycle regulator
HSPG2 heparan sulfate proteoglycan 2
JMJD1C jumonji domain containing 1C
NHP2 NHP2 ribonucleoprotein
NOP10 NOP10 ribonucleoprotein
PABPN1 poly(A) binding protein, nuclear 1
PARN poly(A)-specific ribonuclease
RREB1 ras responsive element binding protein 1
RTEL1 regulator of telomere elongation helicase 1
SEC24C SEC24 family member C
SOX9 SRY (sex determining region Y)-box 9
TBX1 T-box 1
TERT telomerase reverse transcriptase
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
UFD1 ubiquitin recognition factor in ER associated degradation 1
USB1 U6 snRNA biogenesis 1
WRAP53 WD repeat containing, antisense to TP53