Symbol Name ID |
Msh2
mutS homolog 2 MGI:101816 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Death in early adulthood |
Death in infancy |
Disease(s) Associated with MSH2 | ||
Lynch syndrome |
Mouse Phenotypes | premature death |
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Availability | Mouse Genotype | |
Msh2tm1Htr/Msh2tm1Htr | ! | |
Msh2tm1Mak/Msh2tm1Mak | ||
Msh2tm1Rak/Msh2tm1Rak | ||
Msh2tm1Whl/Msh2tm1Whl | ||
Msh2tm2.2Rak/Msh2tm2.2Rak | ||
Msh2tm1Htr/Msh2+ | ||
Msh2tm2.1Rak/Msh2tm2.1Rak Tg(Vil1-cre)20Syr/0 (conditional) |
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 04/23/2024 MGI 6.23 |
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