|
Symbol Name ID |
Mlh1
mutL homolog 1 MGI:101938 |
| Darker colors indicate more annotations |
| Human Phenotypes | Amaurosis fugax |
Visual impairment |
Visual field defect |
| Disease(s) Associated with MLH1 | |||
| Lynch syndrome |
| Mouse Phenotypes | cataract |
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| Availability | Mouse Genotype | |
| Mlh1tm1b(EUCOMM)Hmgu/Mlh1tm1b(EUCOMM)Hmgu | ||
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 04/16/2024 MGI 6.23 |
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