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Symbol Name ID |
Hgf
hepatocyte growth factor MGI:96079 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of chromosome stability |
Chromosome breakage |
| Disease(s) Associated with HGF | ||
| systemic scleroderma |
| Mouse Phenotypes | abnormal melanoblast migration |
decreased hepatocyte proliferation |
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| Availability | Mouse Genotype | ||
| Tg(Mt1-Hgf)19Lmb/0 | |||
| Hgftm1Jmw/Hgftm1Jmw (conditional) | |||
| Hgftm1Jmw/Hgftm1Jmw Tg(Mx1-cre)29-4Her/0 (conditional) |
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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 04/30/2024 MGI 6.23 |
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