Trismus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Limitation in the ability to open the mouth. (Human Phenotype Ontology, HP_0000211)
External Link https://www.disgenet.org/browser/0/1/0/C0041105
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Genes

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

Symbol Name
BCHE butyrylcholinesterase
CRLF1 cytokine receptor-like factor 1
CYP2C8 cytochrome P450, family 2, subfamily C, polypeptide 8
EDNRA endothelin receptor type A
GBA glucosidase, beta, acid
HSPG2 heparan sulfate proteoglycan 2
IRF2BPL interferon regulatory factor 2 binding protein-like
LIFR leukemia inhibitory factor receptor alpha
MYH8 myosin, heavy chain 8, skeletal muscle, perinatal
PHGDH phosphoglycerate dehydrogenase
PNKD paroxysmal nonkinesigenic dyskinesia
PRRT2 proline-rich transmembrane protein 2
PSAT1 phosphoserine aminotransferase 1
SF3B4 splicing factor 3b, subunit 4, 49kDa
SLC25A42 solute carrier family 25, member 42
TGFB1 transforming growth factor, beta 1
TMEM8C transmembrane protein 8C
TPM2 tropomyosin 2 (beta)