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Symbol Name ID |
Pms2
PMS1 homolog2, mismatch repair system component MGI:104288 |
| Darker colors indicate more annotations |
| Human Phenotypes | Death in early adulthood |
Death in infancy |
| Disease(s) Associated with PMS2 | ||
| Lynch syndrome |
| Mouse Phenotypes | premature death |
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| Availability | Mouse Genotype | |
| Pms2tm1.1Wed/Pms2tm1.1Wed | ||
| Pms2tm1Lisk/Pms2tm1Lisk | ||
| Pms2tm2(cre)Lisk/Pms2tm2(cre)Lisk | ||
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 04/09/2024 MGI 6.23 |
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