Subcutaneous Hemorrhage Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description This term refers to an abnormally increased susceptibility to bruising (purpura, petechiae, or ecchymoses). (Human Phenotype Ontology, HP_0001933)
External Link https://www.disgenet.org/browser/0/1/0/C0854107
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Genes

16 genes associated with the disease Subcutaneous Hemorrhage 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
CBS cystathionine-beta-synthase
EPHB2 EPH receptor B2
KRT14 keratin 14, type I
KRT5 keratin 5, type II
MYORG myogenesis regulating glycosidase (putative)
NOTCH3 notch 3
PDGFB platelet-derived growth factor beta polypeptide
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
PTEN phosphatase and tensin homolog
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
SLC35A1 solute carrier family 35 (CMP-sialic acid transporter), member A1
TLR4 toll-like receptor 4
VEGFA vascular endothelial growth factor A
XPR1 xenotropic and polytropic retrovirus receptor 1