skin hemorrhage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description bleeding into the skin (Mammalian Phenotype Ontology, MP_0011514)
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16 gene mutations causing the skin hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
AIP aryl hydrocarbon receptor interacting protein
CLEC1B C-type lectin domain family 1, member B
F2 coagulation factor II (thrombin)
FBLN1 fibulin 1
FERMT3 fermitin family member 3
FGA fibrinogen alpha chain
GAB1 GRB2-associated binding protein 1
GPR4 G protein-coupled receptor 4
HSPG2 heparan sulfate proteoglycan 2
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
PDGFRB platelet-derived growth factor receptor, beta polypeptide
RAMP2 receptor (G protein-coupled) activity modifying protein 2
SCG5 secretogranin V
SELP selectin P (granule membrane protein 140kDa, antigen CD62)
TREML1 triggering receptor expressed on myeloid cells-like 1