ulnar deviation of the wrist Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003049
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Genes

8 genes associated with the ulnar deviation of the wrist phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
COMP cartilage oligomeric matrix protein
GALNS galactosamine (N-acetyl)-6-sulfatase
GLB1 galactosidase, beta 1
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
TNNI2 troponin I type 2 (skeletal, fast)
TNNT3 troponin T type 3 (skeletal, fast)
TPM2 tropomyosin 2 (beta)