malar prominence Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Prominence of the malar process of the maxilla and infraorbital area appreciated in profile and from in front of the face. (Human Phenotype Ontology, HP_0010620)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010620
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Genes

4 genes associated with the malar prominence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
DLX3 distal-less homeobox 3
HBB hemoglobin, beta
NBN nibrin