Abnormality Of The Nares Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormality of the nostril. (Human Phenotype Ontology, HP_0005288)
External Link https://www.disgenet.org/browser/0/1/0/C4021637
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Genes

8 genes associated with the disease Abnormality Of The Nares in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
HMGA2 high mobility group AT-hook 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LEMD3 LEM domain containing 3
MTM1 myotubularin 1
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
SOX11 SRY (sex determining region Y)-box 11
SPART spartin
UBR1 ubiquitin protein ligase E3 component n-recognin 1