Talon Cusp Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Talon cusp is an accessory cusp located near the cingulum (the portion of the lingual or palatal aspect of the tooth that forms a convex protuberance at the cervical third of the anatomic crown). (Human Phenotype Ontology, HP_0011087)
External Link https://www.disgenet.org/browser/0/1/0/C0399357
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Genes

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

Symbol Name
BCOR BCL6 corepressor
CHSY1 chondroitin sulfate synthase 1
CREBBP CREB binding protein
EP300 E1A binding protein p300
NEK1 NIMA-related kinase 1