aplasia/hypoplasia involving the carpal bones Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the carpal bones. (Human Phenotype Ontology, HP_0006502)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006502
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Genes

11 genes associated with the aplasia/hypoplasia involving the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COMP cartilage oligomeric matrix protein
DYM dymeclin
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
KIF22 kinesin family member 22
LMBR1 limb development membrane protein 1
RBM8A RNA binding motif protein 8A
RECQL4 RecQ protein-like 4
SALL4 spalt-like transcription factor 4
TRPV4 transient receptor potential cation channel, subfamily V, member 4
WNT7A wingless-type MMTV integration site family, member 7A