intracranial hemorrhage Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hemorrhage occurring within the skull. (Human Phenotype Ontology, HP_0002170)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002170
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Genes

42 genes associated with the intracranial hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
ACVRL1 activin A receptor type II-like 1
ALPL alkaline phosphatase, liver/bone/kidney
APP amyloid beta (A4) precursor protein
ATP7A ATPase, Cu++ transporting, alpha polypeptide
CBS cystathionine-beta-synthase
CECR1 cat eye syndrome chromosome region, candidate 1
COL4A2 collagen, type IV, alpha 2
CPT2 carnitine palmitoyltransferase 2
CST3 cystatin C
DOCK8 dedicator of cytokinesis 8
ENG endoglin
F10 coagulation factor X
F13A1 coagulation factor XIII, A1 polypeptide
F7 coagulation factor VII (serum prothrombin conversion accelerator)
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGG fibrinogen gamma chain
FN1 fibronectin 1
GATA2 GATA binding protein 2
GBA glucosidase, beta, acid
GCDH glutaryl-CoA dehydrogenase
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
IVD isovaleryl-CoA dehydrogenase
JAK2 Janus kinase 2
KIF1B kinesin family member 1B
KRIT1 KRIT1, ankyrin repeat containing
MUT methylmalonyl CoA mutase
NOTCH3 notch 3
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
PDCD10 programmed cell death 10
PTEN phosphatase and tensin homolog
RET ret proto-oncogene
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SH2B3 SH2B adaptor protein 3
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1