mesomelia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Shortening of the middle parts of the limbs (forearm and lower leg) in relation to the upper and terminal segments. (Human Phenotype Ontology, HP_0003027)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003027
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Genes

10 genes associated with the mesomelia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACAN aggrecan
FLNA filamin A, alpha
GDF5 growth differentiation factor 5
IFT80 intraflagellar transport 80
LBR lamin B receptor
NPR2 natriuretic peptide receptor 2
ROR2 receptor tyrosine kinase-like orphan receptor 2
SHOX short stature homeobox
TBX15 T-box 15
WNT5A wingless-type MMTV integration site family, member 5A