ELN Chromosome 7

Elastin
217 variants 217 Health Risk

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What This Gene Does
This gene encodes a protein that is one of the two components of elastic fibers. Elastic fibers comprise part of the extracellular matrix and confer elasticity to organs and tissues including the heart, skin, lungs, ligaments, and blood vessels. The encoded protein is rich in hydrophobic amino acids such as glycine and proline, which form mobile hydrophobic regions bounded by crosslinks between lysine residues. Degradation products of the encoded protein, known as elastin-derived peptides or elastokines, bind the elastin receptor complex and other receptors and stimulate migration and proliferation of monocytes and skin fibroblasts. Elastokines can also contribute to cancer progression. Deletions and mutations in this gene are associated with supravalvular aortic stenosis (SVAS) and autosomal dominant cutis laxa. [provided by RefSeq, Aug 2017]
Associated Conditions (22)
Supravalvar aortic stenosis
ELN-related disorder
Cutis laxa
autosomal dominant 1
Familial atrioventricular septal defect
Inborn genetic diseases
Cardiomyopathy
Williams syndrome
See cases
Familial cancer of breast
Hypertelorism
Venous malformation
Dural ectasia
Abnormal digit morphology
Hepatocellular carcinoma
Cervical cancer
autosomal dominant
Familial thoracic aortic aneurysm and aortic dissection
Lung cancer
Thyroid cancer
+2 more conditions
Key Variants
RS1230920104
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, Supravalvar aortic stenosis
Health Risk
RS1280128851
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, ELN-related disorder, Supravalvar aortic stenosis
Health Risk
RS1304441113
Conflicting classifications of pathogenicity
ELN-related disorder, ELN-related disorder
Health Risk
RS137953195
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, Cutis laxa, autosomal dominant 1
Health Risk
RS138504338
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, Inborn genetic diseases, Supravalvar aortic stenosis
Health Risk
RS138876104
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, Inborn genetic diseases, Supravalvar aortic stenosis
Health Risk
RS139547471
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, ELN-related disorder, Supravalvar aortic stenosis
Health Risk
RS140337204
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, Supravalvar aortic stenosis
Health Risk
RS142316834
Conflicting classifications of pathogenicity
Cutis laxa, autosomal dominant 1, Supravalvar aortic stenosis
Health Risk
RS1440841207
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, Supravalvar aortic stenosis
Health Risk
RS145519139
Conflicting classifications of pathogenicity
Cutis laxa, autosomal dominant 1, Supravalvar aortic stenosis
Health Risk
RS145612009
Conflicting classifications of pathogenicity
Supravalvar aortic stenosis, Cutis laxa, autosomal dominant 1
Health Risk
All Variants (217)
RSID Category Clinical Significance Conditions
RS781857513 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Cutis laxa, autosomal dominant 1
RS781904032 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, ELN-related disorder, Supravalvar aortic stenosis
RS781963804 Health Risk Conflicting classifications of pathogenicity Cutis laxa, autosomal dominant 1, Supravalvar aortic stenosis
RS782096458 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, ELN-related disorder, Supravalvar aortic stenosis
RS782202364 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Cutis laxa, autosomal dominant 1
RS782225994 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS782238382 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Inborn genetic diseases, Supravalvar aortic stenosis
RS782279081 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Familial thoracic aortic aneurysm and aortic dissection, Supravalvar aortic stenosis
RS782285456 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Cutis laxa, autosomal dominant 1
RS782388951 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Cutis laxa, autosomal dominant 1
RS782393234 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS782493042 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Inborn genetic diseases, Supravalvar aortic stenosis
RS782643005 Health Risk Conflicting classifications of pathogenicity
RS782739997 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS782745619 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS782770862 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Lung cancer, Supravalvar aortic stenosis
RS782790041 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Cutis laxa, autosomal dominant 1
RS782791376 Health Risk Conflicting classifications of pathogenicity Williams syndrome, Supravalvar aortic stenosis, Williams syndrome
RS782794260 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Thyroid cancer, nonmedullary
RS934014841 Health Risk Conflicting classifications of pathogenicity Supravalvar aortic stenosis, Cutis laxa, autosomal dominant 1
RS1008236555 Health Risk Likely pathogenic
RS1131691482 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS1284902357 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS1554669592 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS1554669774 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS1554688700 Health Risk Likely pathogenic
RS1563793627 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS1583818183 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS1583822018 Health Risk Likely pathogenic
RS1583873953 Health Risk Likely pathogenic
RS1795220933 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS1797218441 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS2131152526 Health Risk Likely pathogenic
RS2131602837 Health Risk Likely pathogenic
RS2132828209 Health Risk Likely pathogenic Cutis laxa, autosomal dominant 1, Supravalvar aortic stenosis
RS2484783425 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS2484848631 Health Risk Likely pathogenic
RS2485064649 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS2485184528 Health Risk Likely pathogenic
RS2485451259 Health Risk Likely pathogenic ELN-related disorder, ELN-related disorder
RS2485516621 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS2485893388 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS2486286311 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS2486325853 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS2486525314 Health Risk Likely pathogenic ELN-related disorder, ELN-related disorder
RS2486723583 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS565632539 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS727503026 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS727503031 Health Risk Likely pathogenic Supravalvar aortic stenosis, Supravalvar aortic stenosis
RS781908666 Health Risk Likely pathogenic
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