abnormality of the fingertips Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001211
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11 genes associated with the abnormality of the fingertips phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CREBBP CREB binding protein
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
KANSL1 KAT8 regulatory NSL complex subunit 1
KDM6A lysine (K)-specific demethylase 6A
KMT2D lysine (K)-specific methyltransferase 2D
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
MED12 mediator complex subunit 12
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
PTH1R parathyroid hormone 1 receptor
SFTPA2 surfactant protein A2
STK11 serine/threonine kinase 11