Summary |
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Variant origin |
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Variant description |
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Phenotypes |
View phenotypes and curated references for all genotypes (concatenated display).
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Notes |
Pecam1
Mapping and Phenotype information for this QTL, its variants and associated markersJ:144817The Pecam1tm1Mak knockout allele on an FVB/N genetic background results in impaired inflammatory response due to a blockade in leukocyte transendothelial migration. However, when Pecam1tm1Mak is on a C57BL/6 genetic background inflammatory response and diapedesis are not impaired. Genetic modifiers responsible for this phenomenon were mapped by screening 150 polymorphic marker in a population of (B6.129P2-Pecam1tm1Mak x FVB/N-Pecam1tm1Mak)F2 intercross animals. Inflammatory response was measured after thioglycollate administration. Significant linkage to inflammatory response mapped to proximal mouse Chromosome 2 at 28 cM (38.2 Mb) near D2Mit7 (LOD=7.5). This locus is designated Pitgp (Pecam1-independent thioglycollate peritonitis). Additional analysis of Pitgp using medium-density mapping refined the QTL location to 35.8 Mb and increased the LOD score to 9.0. Four potential candidate genes are located near Pitgp: Ptgs1 (29 cM), Ptges (24 cM), Ptges2 and Hc (23.5 cM). C57BL/6-derived alleles atPitgp confer Pecam1-independent inflammatory response in a thioglycollate model of peritonitis, and appears to exhibit dominant inheritance. Authors speculate the gene responsible for Pitgp is a gain-of-function variant. |
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References |
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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 12/10/2024 MGI 6.24 |
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