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Cctq3SJL/J
QTL Variant Detail
Summary
QTL variant: Cctq3SJL/J
Name: central corneal thickness QTL 3; SJL/J
MGI ID: MGI:5693533
QTL: Cctq3  Location: unknown  Genetic Position: Chr17, Syntenic
Variant
origin
Strain of Specimen:  SJL/J
Variant
description
Allele Type:    QTL
Inheritance:    Not Specified
Notes

Mapping and Phenotype information for this QTL, its variants and associated markers

J:163199

A genome wide scan using 92 (KS X SJL) F2 mice proved informative to identify CCtq1 on mouse Chromosome 7 with a max LOD score -2.87 at 115 Mb with a interval extending from 65 to 139 Mb. CCtq1 was further characterized by a max LOD score of 3.28 at 105 Mb with a peak at D7Mit321

In addition 84 (KS X NZB)F2 mice were utilized to confirm the existence of the chromosome 7 locus.

F2 mice identified one suggestive interaction between loci on mouse Chromosome 11 (Cctq2, 21.3 Mb) and another suggestive locus on mouse chromosome 17 (Cctq3, 92.7 Mb).

References
Original:  J:163199 Lively GD, et al., Quantitative trait loci associated with murine central corneal thickness. Physiol Genomics. 2010 Jul 7;42(2):281-6
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory