abnormality of primary teeth Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the primary tooth. (Human Phenotype Ontology, HP_0006481)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0006481
Similar Terms
Downloads & Tools

Genes

19 genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1 1.75646
ADK adenosine kinase 1.75396
HMGA2 high mobility group AT-hook 2 1.43716
MSRB3 methionine sulfoxide reductase B3 1.32793
CACNB2 calcium channel, voltage-dependent, beta 2 subunit 1.32793
OPN1SW opsin 1 (cone pigments), short-wave-sensitive 1.29386
RAD51B RAD51 paralog B 1.19958
C14ORF93 chromosome 14 open reading frame 93 1.19958
DLEU7 deleted in lymphocytic leukemia, 7 1.19958
RNF43 ring finger protein 43 1.17433
EDAR ectodysplasin A receptor 1.07428
DLGAP1 discs, large (Drosophila) homolog-associated protein 1 0.974864
EDA ectodysplasin A 0.871758
TEX14 testis expressed 14 0.7965
LOC338667 V-set and immunoglobulin domain-containing protein 10-like 0.722116
SKA2 spindle and kinetochore associated complex subunit 2 0.492728
BMP4 bone morphogenetic protein 4 0.487836
HSF5 heat shock transcription factor family member 5 0.485436
CES4A carboxylesterase 4A 0.412794