Symbol Name ID |
Fgf8
fibroblast growth factor 8 MGI:99604 |
Darker colors indicate more annotations |
Human Phenotypes | Sensorineural hearing impairment |
Disease(s) Associated with FGF8 | |
hypogonadotropic hypogonadism 6 with or without anosmia |
Mouse Phenotypes | abnormal pillar cell differentiation |
absent incus |
abnormal cochlear sensory epithelium morphology |
abnormal pillar cell morphology |
absent pillar cells |
abnormal patterning of the organ of Corti |
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Availability | Mouse Genotype | ||||||
Fgf8tm1.2Mrt/Fgf8tm1.3Mrt Tg(Nes-cre)1Atp/0 (conditional) |
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Fgf8tm1.2Mrt/Fgf8tm1.3Mrt Foxg1tm1(cre)Skm/Foxg1+ (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 04/16/2024 MGI 6.23 |
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