abnormality of the columella Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the columella. (Human Phenotype Ontology, HP_0009929)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009929
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Genes

12 genes associated with the abnormality of the columella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX3 ALX homeobox 3
CREBBP CREB binding protein
GJA1 gap junction protein, alpha 1, 43kDa
HDAC4 histone deacetylase 4
KCTD1 potassium channel tetramerization domain containing 1
KDM6A lysine (K)-specific demethylase 6A
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NOG noggin
SRCAP Snf2-related CREBBP activator protein
THOC6 THO complex 6
ZEB2 zinc finger E-box binding homeobox 2