EPHB4 Chromosome 7

EPH receptor B4
154 variants 154 Health Risk

Upload your DNA to see your personal genotypes for variants in EPHB4.

What This Gene Does
Ephrin receptors and their ligands, the ephrins, mediate numerous developmental processes, particularly in the nervous system. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Ephrin receptors make up the largest subgroup of the receptor tyrosine kinase (RTK) family. The protein encoded by this gene binds to ephrin-B2 and plays an essential role in vascular development. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Sterile alpha motif domain containing|EPH receptors"
Locus Type
gene with protein product
Location
7q22.1
Ensembl
ENSG00000196411
Associated Conditions (10)
Vein of Galen aneurysmal malformation
Cardiovascular phenotype
EPHB4-related disorder
Capillary malformation-arteriovenous malformation 2
Lymphatic malformation 7
Venous malformation
EPHB4-associated vascular malformation spectrum
Arteriovenous malformation
Hereditary lymphedema type I
Capillary malformation-arteriovenous malformation syndrome
Key Variants
RS2116449991
association
Vein of Galen aneurysmal malformation, Vein of Galen aneurysmal malformation
Health Risk
RS1056350781
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS111749768
Conflicting classifications of pathogenicity
Cardiovascular phenotype, EPHB4-related disorder, Capillary malformation-arteriovenous malformation 2
Health Risk
RS114926839
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1159930961
Conflicting classifications of pathogenicity
Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2
Health Risk
RS1330628156
Conflicting classifications of pathogenicity
Capillary malformation-arteriovenous malformation 2, EPHB4-related disorder, Capillary malformation-arteriovenous malformation 2
Health Risk
RS140842916
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS141544967
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS142856240
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS146902369
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS147563837
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1584652949
Conflicting classifications of pathogenicity
Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2
Health Risk
All Variants (154)
RSID Category Clinical Significance Conditions
RS1812821716 Health Risk Pathogenic Lymphatic malformation 7, EPHB4-related disorder, Lymphatic malformation 7
RS1812969416 Health Risk Pathogenic
RS1813100007 Health Risk Pathogenic
RS1813191696 Health Risk Pathogenic
RS1813260006 Health Risk Pathogenic
RS1813316083 Health Risk Pathogenic
RS1813316337 Health Risk Pathogenic
RS2116413904 Health Risk Pathogenic Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2
RS2116413948 Health Risk Pathogenic Arteriovenous malformation, Arteriovenous malformation
RS2116431707 Health Risk Pathogenic Hereditary lymphedema type I, Hereditary lymphedema type I
RS2116431816 Health Risk Pathogenic
RS2116451858 Health Risk Pathogenic
RS2116458223 Health Risk Pathogenic
RS2116461878 Health Risk Pathogenic EPHB4-related disorder, EPHB4-related disorder
RS2116461987 Health Risk Pathogenic
RS2116462820 Health Risk Pathogenic Capillary malformation-arteriovenous malformation syndrome, Capillary malformation-arteriovenous malformation syndrome
RS2485000657 Health Risk Pathogenic Capillary malformation-arteriovenous malformation syndrome, Capillary malformation-arteriovenous malformation syndrome
RS2485000821 Health Risk Pathogenic Cardiovascular phenotype, Cardiovascular phenotype
RS2485000836 Health Risk Pathogenic Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2
RS2485016159 Health Risk Pathogenic
RS2485016589 Health Risk Pathogenic
RS2485017389 Health Risk Pathogenic
RS2485028164 Health Risk Pathogenic
RS2485028768 Health Risk Pathogenic
RS2485035566 Health Risk Pathogenic Cardiovascular phenotype, Cardiovascular phenotype
RS2485035644 Health Risk Pathogenic
RS2485036149 Health Risk Pathogenic
RS2485038099 Health Risk Pathogenic
RS2485046175 Health Risk Pathogenic
RS2485049009 Health Risk Pathogenic
RS2485049740 Health Risk Pathogenic Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2
RS2485050114 Health Risk Pathogenic
RS746199977 Health Risk Pathogenic Cardiovascular phenotype, Cardiovascular phenotype
RS749250094 Health Risk Pathogenic
RS749503755 Health Risk Pathogenic Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2
RS750862933 Health Risk Pathogenic
RS767827881 Health Risk Pathogenic Capillary malformation-arteriovenous malformation 2, Lymphatic malformation 7, Capillary malformation-arteriovenous malformation 2
RS773967187 Health Risk Pathogenic Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2
RS779782731 Health Risk Pathogenic Capillary malformation-arteriovenous malformation syndrome, Capillary malformation-arteriovenous malformation syndrome
RS780186346 Health Risk Pathogenic EPHB4-related disorder, EPHB4-related disorder
RS927772349 Health Risk Pathogenic Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2, Capillary malformation-arteriovenous malformation 2
RS994651018 Health Risk Pathogenic
RS1049858988 Health Risk Pathogenic/Likely pathogenic
RS1279971868 Health Risk Pathogenic/Likely pathogenic Capillary malformation-arteriovenous malformation 2, Lymphatic malformation 7, Capillary malformation-arteriovenous malformation 2
RS1331371272 Health Risk Pathogenic/Likely pathogenic Capillary malformation-arteriovenous malformation 2, Cardiovascular phenotype, Capillary malformation-arteriovenous malformation 2
RS1562967226 Health Risk Pathogenic/Likely pathogenic EPHB4-related disorder, EPHB4-related disorder
RS1562969219 Health Risk Pathogenic/Likely pathogenic Capillary malformation-arteriovenous malformation 2, EPHB4-related disorder, Capillary malformation-arteriovenous malformation 2
RS2116434296 Health Risk Pathogenic/Likely pathogenic Capillary malformation-arteriovenous malformation 2, Lymphatic malformation 7, Capillary malformation-arteriovenous malformation 2
RS2116435260 Health Risk Pathogenic/Likely pathogenic EPHB4-related disorder, EPHB4-related disorder
RS370570826 Health Risk Pathogenic/Likely pathogenic
Sign Up to Analyze Your DNA Log In