Abnormality Of The Gingiva Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Any abnormality of the gingiva (also known as gums). (Human Phenotype Ontology, HP_0000168)
External Link https://www.disgenet.org/browser/0/1/0/C4021816
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Genes

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

Symbol Name
COL1A1 collagen, type I, alpha 1
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
ECM1 extracellular matrix protein 1
KLLN killin, p53-regulated DNA replication inhibitor
MBTPS2 membrane-bound transcription factor peptidase, site 2
NEK1 NIMA-related kinase 1
NGF nerve growth factor (beta polypeptide)
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PERP PERP, TP53 apoptosis effector
SETBP1 SET binding protein 1
TCTN3 tectonic family member 3
TRPV3 transient receptor potential cation channel, subfamily V, member 3