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Symbol Name ID |
Hgf
hepatocyte growth factor MGI:96079 |
| Darker colors indicate more annotations |
| Human Phenotypes | Prelingual sensorineural hearing impairment |
| Disease(s) Associated with HGF | |
| autosomal recessive nonsyndromic deafness 39 |
| Mouse Phenotypes | increased ear pigmentation |
decreased cochlear outer hair cell number |
cochlear outer hair cell degeneration |
abnormal organ of Corti supporting cell morphology |
organ of Corti degeneration |
spiral ligament degeneration |
abnormal stria vascularis morphology |
abnormal strial intermediate cell morphology |
thin stria vascularis |
decreased endocochlear potential |
abnormal distortion product otoacoustic emission |
impaired hearing |
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| Availability | Mouse Genotype | ||||||||||||
| Hgftm1.1Tbf/Hgftm1.1Tbf | |||||||||||||
| Hgftm1Tbf/Hgftm1Tbf | |||||||||||||
| Tg(Mt1-Hgf)#Lmb/0 | |||||||||||||
| Hgftm1Jmw/Hgftm1Jmw Tg(Pax2-cre)1Akg/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 05/14/2024 MGI 6.23 |
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