EFEMP2 Chromosome 11

EGF-like fibulin extracellular matrix protein 2
56 variants 56 Health Risk

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What This Gene Does
A large number of extracellular matrix proteins have been found to contain variations of the epidermal growth factor (EGF) domain and have been implicated in functions as diverse as blood coagulation, activation of complement and determination of cell fate during development. The protein encoded by this gene contains four EGF2 domains and six calcium-binding EGF2 domains. This gene is necessary for elastic fiber formation and connective tissue development. Defects in this gene are cause of an autosomal recessive cutis laxa syndrome. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jan 2011]
Gene Info
Gene Group
Fibulins
Locus Type
gene with protein product
Location
11q13.1
Ensembl
ENSG00000172638
Associated Conditions (9)
Cutis laxa
autosomal recessive
type 1B
Cardiovascular phenotype
Familial thoracic aortic aneurysm and aortic dissection
EFEMP2-related disorder
Ovarian serous cystadenocarcinoma
type 1A
Familial aortopathy
Key Variants
All Variants (56)
RSID Category Clinical Significance Conditions
RS113167523 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS1224841813 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS1306393544 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS140946753 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS141868759 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS142509316 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS1442174846 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS148315164 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS148410446 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS149525720 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS187686630 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS188624478 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS199606204 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS2234473 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS376275864 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS377139656 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS532989312 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS546162289 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS554639118 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS572394429 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS61740381 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS746343857 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS762409753 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS779131358 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal recessive, type 1B
RS1064796673 Health Risk Likely pathogenic
RS119489102 Health Risk Likely pathogenic Cutis laxa, autosomal recessive, type 1B
RS1555042727 Health Risk Likely pathogenic Cutis laxa, autosomal recessive, type 1B
RS1859863045 Health Risk Likely pathogenic Cardiovascular phenotype, Cardiovascular phenotype
RS1859902707 Health Risk Likely pathogenic Cutis laxa, autosomal recessive, type 1B
RS1859976995 Health Risk Likely pathogenic Cutis laxa, autosomal recessive, type 1B
RS2495574266 Health Risk Likely pathogenic
RS2495579185 Health Risk Likely pathogenic Cutis laxa, autosomal recessive, type 1B
RS2495583852 Health Risk Likely pathogenic Cutis laxa, autosomal recessive, type 1B
RS57685603 Health Risk Likely pathogenic Cutis laxa, Cutis laxa
RS888015688 Health Risk Likely pathogenic Cutis laxa, autosomal recessive, type 1B
RS1044449024 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS119489101 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1A
RS1267180414 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS1565274421 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS1591064775 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS1859884792 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS1859949436 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS193302865 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS193302866 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1A
RS193302868 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1A
RS193302869 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1A
RS193302870 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS2134747667 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS2495573872 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
RS2495580444 Health Risk Pathogenic Cutis laxa, autosomal recessive, type 1B
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