GeneSet Information

Tier II GS135678 • compensatory renal hypertrophy QTL 1 (Crhq1, Published QTL Chr 11)

DESCRIPTION:

QTL associated with compensatory renal hypertrophy QTL 1. This interval was obtained by using a fixed interval width of 25 Mbp around the peak marker (98544969)

LABEL:

QTL-Crhq1-Mouse-Chr 11

SCORE TYPE:

Binary

DATE ADDED:

2012-04-02

DATE UPDATED:

2020-05-06

SPECIES:

AUTHORS:

Zdek V, Musilov A, Vorlek J, Simkov M, Pravenec M

TITLE:

Quantitative trait loci for compensatory renal hypertrophy in the mouse.

JOURNAL:

Biochemical and biophysical research communications Jul 1998, Vol 248, pp. 473-5

ABSTRACT:

Reduction in numbers of nephrons or decrease in kidney function due to a variety of diseases results in compensatory renal hypertrophy (CRH). Recently, it has been proposed that CRH may be a prerequisite for progression of renal injury; genetic dissection of CRH may be therefore helpful in understanding the process whereby people with partial renal insufficiency progress to end-stage renal disease. Since genetic analysis of CRH in humans is quite limited, we searched for genetic determinants of CRH after unilateral nephrectomy using a total genome scan of the mouse BXD recombinant inbred strains. We demonstrated that CRH is a highly heritable trait and we identified a quantitative trait locus on mouse chromosome 11 near the D11Mit14 marker that exerts a major effect on CRH (lod score = 3.4) and is responsible for approximately 52% of genetic variation in CRH. This marker maps near Ace, Gh, and Ngfr positional candidate genes. PUBMED: 9703949
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Annotation Information

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Genetic Variation (D014644)
Renal Insufficiency (D051437)
Corticotropin-Releasing Hormone (D003346)
Chromosomes (D002875)
Comprehension (D032882)
Quantitative Trait Loci (D040641)
Dissection (D004210)
Nephrons (D009399)
Kidney Failure, Chronic (D007676)
Wounds and Injuries (D014947)
Chromosomes, Human, Pair 11 (D002880)
Hypertrophy (D006984)
Nephrectomy (D009392)
chromosome (GO:0005694)

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