aplasia/hypoplasia of the humerus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence (due to failure to form) or underdevelopment of the humerus. (Human Phenotype Ontology, HP_0006507)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006507
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18 genes associated with the aplasia/hypoplasia of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPS alkylglycerone phosphate synthase
ATP7A ATPase, Cu++ transporting, alpha polypeptide
FLNA filamin A, alpha
FLNB filamin B, beta
GDF5 growth differentiation factor 5
GNPAT glyceronephosphate O-acyltransferase
GPC6 glypican 6
GSC goosecoid homeobox
IFT122 intraflagellar transport 122
IHH indian hedgehog
LMBR1 limb development membrane protein 1
NOG noggin
RBM8A RNA binding motif protein 8A
RECQL4 RecQ protein-like 4
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SALL4 spalt-like transcription factor 4
TBX3 T-box 3
ZIC3 Zic family member 3