Capillary Malformation-Arteriovenous Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1842180
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Genes

25 genes associated with the disease Capillary Malformation-Arteriovenous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
ARF3 ADP-ribosylation factor 3
BRD8 bromodomain containing 8
CCM2 cerebral cavernous malformation 2
CCNH cyclin H
CTNND1 catenin (cadherin-associated protein), delta 1
ENG endoglin
EPHB4 EPH receptor B4
HNRNPU heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A)
IGSF1 immunoglobulin superfamily, member 1
MEF2C myocyte enhancer factor 2C
NAA25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit
NOP2 NOP2 nucleolar protein
NSUN5 NOP2/Sun domain family, member 5
RAB1B RAB1B, member RAS oncogene family
RAB6B RAB6B, member RAS oncogene family
RAP1B RAP1B, member of RAS oncogene family
RAP2B RAP2B, member of RAS oncogene family
RASA1 RAS p21 protein activator (GTPase activating protein) 1
RASA2 RAS p21 protein activator 2
SLC12A9 solute carrier family 12, member 9
SMAD4 SMAD family member 4
SPRED1 sprouty-related, EVH1 domain containing 1
STAMBP STAM binding protein
SYNGAP1 synaptic Ras GTPase activating protein 1