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 |
|
Availability | Mouse Genotype | ||
Tg(Mt1-Hgf)19Lmb/0 | |||
Hgftm1Jmw/Hgftm1Jmw (conditional) | |||
Hgftm1Jmw/Hgftm1Jmw Tg(Mx1-cre)29-4Her/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 08/21/2024 MGI 6.24 |
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