abnormality of the achilles tendon Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the Achilles tendon. (Human Phenotype Ontology, HP_0005109)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005109
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Genes

13 genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABHD12 abhydrolase domain containing 12
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
BICD2 bicaudal D homolog 2 (Drosophila)
COL6A2 collagen, type VI, alpha 2
EMD emerin
FKRP fukutin related protein
GJB1 gap junction protein, beta 1, 32kDa
HGD homogentisate 1,2-dioxygenase
HRAS Harvey rat sarcoma viral oncogene homolog
LARGE like-glycosyltransferase
LMNA lamin A/C
MYOT myotilin
NSUN2 NOP2/Sun RNA methyltransferase family, member 2