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Article

R1615P: a novel mutation in ABCA1 associated with low levels of HDL and type II diabetes mellitus.

International journal of cardiology - 16 Jun 2006

Saleheen Danish, Nazir Aisha, Khanum Shaheen, Haider Shajjia R, Frossard Philippe M

Abstract excerpt

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Topics

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Share to Amino Acid Substitution
Share to ATP Binding Cassette Transporter 1
Share to ATP-Binding Cassette Transporters

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cholesterol, HDL

Share to Conserved Sequence

Share to Diabetes Mellitus, Type 2

Share to Proline

Share to Sequence Homology, Amino Acid

Source

Identifiers

PMID: 16055210
DOI: 10.1016/j.ijcard.2005.06.059

Genes

ABCA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

R1615P: a novel mutation in ABCA1 associated with low levels of HDL and type II diabetes mellitus.PMID 16055210Read ↗

Association of HDL deficiency with a novel mutation in the ABCA1 gene.Semantic proximity Read ↗

Variations on a gene: rare and common variants in ABCA1 and their impact on HDL cholesterol levels and atherosclerosis.Semantic proximity Read ↗

A novel nonsense mutation of ABCA8 in a patient with reduced HDL-c levels and atherosclerosis.Semantic proximity Read ↗

Novel rare mutations and promoter haplotypes in ABCA1 contribute to low-HDL-C levels.Semantic proximity Read ↗

The Role of the ATP-Binding Cassette A1 (ABCA1) in Human Disease.Semantic proximity Read ↗

Identification and Molecular Simulation of Genetic Variants in ABCA1 Gene Associated with Susceptibility to Dyslipidemia in Type 2 Diabetes.Semantic proximity Read ↗

The ATP-binding cassette transporter subfamily A member 1 (ABC-A1) and type 2 diabetes: an association beyond HDL cholesterol.Semantic proximity Read ↗

Genetic disorders associated with ATP binding cassette cholesterol transporters.Semantic proximity Read ↗

Screening for functional sequence variations and mutations in ABCA1.Semantic proximity Read ↗

The Arg1379His mutation in ABCC8 causes monogenic diabetes with variable phenotype presentation and incomplete penetrance.Semantic proximity Read ↗

Single heterozygote splice mutation in the ABCA1 gene is associated with diffuse atherosclerotic disease in a low high-density lipoprotein syndrome.Semantic proximity Read ↗

A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large familySemantic proximity Read ↗

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