Evidence map›Paper›PMID 18988887›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2009

Farp2 and Stk25 are candidate genes for the HDL cholesterol locus on mouse chromosome 1.

Zhiguang Su, Allison Cox, Yuan Shen, Ioannis M Stylianou, Beverly Paigen

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Deletion of Nrip1 Extends Female Mice Longevity, Increases Autophagy, and Delays Cell Senescence.The journals of gerontology. Series A, Biological sciences and medical sciences · 2018
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Zhiguang SuThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Allison Cox
Yuan Shen
Ioannis M Stylianou
Beverly Paigen
Jackson Laboratory · US

Funding

From QTL to Gene for HDL CholesterolR37HL077796 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2009 to 2018
$4.3M
Cloning QTL Genes for Plasma HDL CholesterolR01HL081162 · NHLBI · JACKSON LABORATORY · PI KORSTANJE, RONNY · 2006 to 2013
$3.3M
From QTL to Gene for HDL CholesterolR01HL077796 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2004 to 2008
$2.1M
Identifying Genes Regulating HDL Cholesterol LevelsR01HL074086 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2004 to 2007
$994k
NHLBI NIH HHS HL74086NHLBI NIH HHS HL77796NHLBI NIH HHS HL81162NHLBI NIH HHS R01 HL074086NHLBI NIH HHS R01 HL077796NHLBI NIH HHS R01 HL081162NHLBI NIH HHS R37 HL077796
6 · The paper itself

Abstract

objectiveTo identify the gene responsible for the quantitative trait locus (QTL) Hdlq14, a high-density lipoprotein cholesterol (HDL) QTL previously identified in a C57BL/6Jx129S1/SvImJ cross. METHODS AND

resultsHdlq14 was first confirmed as an independent QTL by detecting it in an intercross between NZB/B1NJ and NZW/LacJ, 2 strains that had identical genotypes at nearby QTL genes on chromosome 1. Using the bioinformatics tools of combined cross data and haplotype analysis, we narrowed this QTL from a 45-Mb 225-gene region to 2 genes, Farp2 and Stk25. Sequencing and expression studies showed that Farp2 had an amino acid polymorphism in an important plekstrin domain and that Stk25 had a significant expression difference between the parental strains. These 2 genes are immediately adjacent to each other and share the same haplotype over 45 inbred strains. The haplotype was associated with a significant difference in HDL levels among these strains.

conclusionsWe confirmed Hdlq14 as a separate independent QTL for HDL and narrowed the region to 2 genes, Farp2 and Stk25, with considerable evidence for both. Additional studies are needed to choose between these 2 genes or to show that both are important in determining HDL levels.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAtherosclerosisCholesterol, HDLChromosome MappingChromosomes, MammalianCrosses, GeneticDiet, AtherogenicDisease Models, AnimalFemaleGenotypeGuanine Nucleotide Exchange FactorsHippo KinasesIntracellular Signaling Peptides and ProteinsLipoproteins, HDLMaleAdaptor Proteins, Signal TransducingCholesterol, HDLFARP2 protein, mouseGuanine Nucleotide Exchange FactorsHippo KinasesIntracellular Signaling Peptides and ProteinsLipoproteins, HDLProtein Serine-Threonine KinasesStk25 protein, mouse

Identifiers

PMID18988887
PMCPMC2782635
OpenAlexW2166653960

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.