Symbol Name ID |
Mitf
melanogenesis associated transcription factor MGI:104554 |
Darker colors indicate more annotations |
Human Phenotypes | Aganglionic megacolon |
Myelomeningocele |
Disease(s) Associated with MITF | ||
Waardenburg syndrome |
Mouse Phenotypes | abnormal melanoblast morphology |
abnormal cochlear hair cell morphology |
absent retina cone cells |
absent retina rod cells |
abnormal retina photoreceptor morphology |
abnormal photoreceptor inner segment morphology |
absent photoreceptor outer segment |
retina photoreceptor degeneration |
absent optic nerve |
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Availability | Mouse Genotype | |||||||||
Mitfmi-bw/Mitfmi-bw Tg(Dct-lacZ)A12Jkn/0 |
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Mitfmi-ce/Mitfmi-ce | ||||||||||
Mitfmi-di/Mitfmi-di | ||||||||||
Mitfmi-vit/Mitfmi-vit | ||||||||||
MitfMi-wh/MitfMi-wh | ||||||||||
MitfMi/MitfMi | ||||||||||
MitfMi/Mitf+ |
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 04/23/2024 MGI 6.23 |
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