Abnormality Of The Wrist Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormality of the wrist, the structure connecting the hand and the forearm. (Human Phenotype Ontology, HP_0003019)
External Link https://www.disgenet.org/browser/0/1/0/C4021744
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Genes

10 genes associated with the disease Abnormality Of The Wrist in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
ATP7A ATPase, Cu++ transporting, alpha polypeptide
BPTF bromodomain PHD finger transcription factor
COL2A1 collagen, type II, alpha 1
DYM dymeclin
FN1 fibronectin 1
LMBR1 limb development membrane protein 1
PSMD12 proteasome (prosome, macropain) 26S subunit, non-ATPase, 12
PTEN phosphatase and tensin homolog
TBX3 T-box 3