Symbol Name ID |
Mitf
melanogenesis associated transcription factor MGI:104554 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the face |
Abnormal facial shape |
Abnormality of the mouth |
Abnormal lip morphology |
Orofacial cleft |
Underdeveloped nasal alae |
Prominent nasal bridge |
Wide nasal bridge |
Abnormal eyebrow morphology |
Synophrys |
White eyebrow |
White eyelashes |
Telecanthus |
Disease(s) Associated with MITF | |||||||||||||
Tietz syndrome | |||||||||||||
Waardenburg syndrome | |||||||||||||
Waardenburg syndrome type 2A |
Mouse Phenotypes | abnormal incisor morphology |
failure of tooth eruption |
decreased ear pigmentation |
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Availability | Mouse Genotype | |||
MitfMi-Crc/MitfMi-Crc | ||||
MitfMi-Or/MitfMi-Or | ||||
MitfMi/MitfMi | ||||
MitfMi-b/Mitf+ | ||||
MitfMi-H/Mitf+ | ||||
MitfMi-Or/Mitf+ | ||||
MitfMi-wh/Mitfmi-sp | ||||
MitfRorp/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 04/16/2024 MGI 6.23 |
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