abnormality of dental color Gene Set
Genes
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)
|