abnormality of dental eruption Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of tooth eruption. (Human Phenotype Ontology, HP_0006292)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0006292
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Genes

17 genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
ADK adenosine kinase 1.68942
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit 1.48687
HMGA2 high mobility group AT-hook 2 1.13699
BMP4 bone morphogenetic protein 4 0.931027
RAD51B RAD51 paralog B 0.810077
MSRB3 methionine sulfoxide reductase B3 0.686884
EDA ectodysplasin A 0.48251
TEX14 testis expressed 14 0.416272
LOC338667 V-set and immunoglobulin domain-containing protein 10-like 0.400092
SKA2 spindle and kinetochore associated complex subunit 2 0.394267
HSF5 heat shock transcription factor family member 5 0.392655
CACNB2 calcium channel, voltage-dependent, beta 2 subunit 0.390094
OPN1SW opsin 1 (cone pigments), short-wave-sensitive 0.389412
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1 0.378502
CES4A carboxylesterase 4A 0.369726
C14ORF93 chromosome 14 open reading frame 93 0.359537
DLEU7 deleted in lymphocytic leukemia, 7 0.323009