broad palm Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description For children from birth to 4 years of age the palm width is more than 2 SD above the mean; for children from 4 to 16 years of age the palm width is above the 95th centile; or, the width of the palm appears disproportionately wide for the length. (Human Phenotype Ontology, HP_0001169)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001169
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Genes

16 genes associated with the broad palm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
ASXL1 additional sex combs like transcriptional regulator 1
COL2A1 collagen, type II, alpha 1
DYM dymeclin
FBN1 fibrillin 1
FGD1 FYVE, RhoGEF and PH domain containing 1
FGFR1 fibroblast growth factor receptor 1
GATA1 GATA binding protein 1 (globin transcription factor 1)
GPC3 glypican 3
IFT80 intraflagellar transport 80
IHH indian hedgehog
LBR lamin B receptor
OFD1 oral-facial-digital syndrome 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
RAI1 retinoic acid induced 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3