Abnormal Diaphysis Morphology Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the structure or form of the diaphysis, i.e., of the main or mid-section (shaft) of a long bone. (Human Phenotype Ontology, HP_0000940)
External Link https://www.disgenet.org/browser/0/1/0/C4021787
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Genes

11 genes associated with the disease Abnormal Diaphysis Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ANTXR2 anthrax toxin receptor 2
COL11A1 collagen, type XI, alpha 1
COL11A2 collagen, type XI, alpha 2
GJA1 gap junction protein, alpha 1, 43kDa
IDUA iduronidase, alpha-L-
IFT122 intraflagellar transport 122
IFT43 intraflagellar transport 43
IFT52 intraflagellar transport 52
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
WDR19 WD repeat domain 19
WDR35 WD repeat domain 35