abnormality of dental color Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect of tooth color. (Human Phenotype Ontology, HP_0011073)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011073
Similar Terms
Downloads & Tools


20 genes associated with the abnormality of dental color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADGRV1 adhesion G protein-coupled receptor V1
CNNM4 cyclin and CBS domain divalent metal cation transport mediator 4
DFNB31 deafness, autosomal recessive 31
DLX3 distal-less homeobox 3
ENAM enamelin
FAM20A family with sequence similarity 20, member A
GALNS galactosamine (N-acetyl)-6-sulfatase
GATA1 GATA binding protein 1 (globin transcription factor 1)
GLB1 galactosidase, beta 1
HRAS Harvey rat sarcoma viral oncogene homolog
KRAS Kirsten rat sarcoma viral oncogene homolog
MBTPS2 membrane-bound transcription factor peptidase, site 2
MYO7A myosin VIIA
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PDZD7 PDZ domain containing 7
ROGDI rogdi homolog (Drosophila)
RUNX2 runt-related transcription factor 2
SAT1 spermidine/spermine N1-acetyltransferase 1
UROS uroporphyrinogen III synthase
USH2A Usher syndrome 2A (autosomal recessive, mild)