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Symbol
Name
ID
Mitf
melanogenesis associated transcription factor
MGI:104554
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Conductive hearing impairment
Sensorineural hearing impairment
Congenital sensorineural hearing impairment
Hearing impairment
Disease(s) Associated with MITF
Tietz syndrome
Waardenburg syndrome
Waardenburg syndrome type 2A

Mouse Phenotypes
decreased ear pigmentation
abnormal inner ear morphology
abnormal cochlea morphology
abnormal cochlear hair cell morphology
abnormal scala media morphology
abnormal stria vascularis morphology
absent strial intermediate cells
thin stria vascularis
abnormal vestibular saccule morphology
abnormal hearing physiology
increased or absent threshold for auditory brainstem response
Availability Mouse Genotype
Mitfmi-bw/Mitfmi-bw
Mitfmi-ce/Mitfmi-ce
MitfMi-wh/MitfMi-wh
MitfMi/MitfMi
MitfMi-b/Mitf+
MitfMi-H/Mitf+
MitfMi-Or/Mitf+
MitfMi-wh/Mitfmi-sp
MitfMi/Mitf+
MitfRorp/Mitf+

Contributing Projects:
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
04/09/2024
MGI 6.23
The Jackson Laboratory