Symbol Name ID |
Kitl
kit ligand MGI:96974 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Conductive hearing impairment |
Sensorineural hearing impairment |
Hearing impairment |
Disease(s) Associated with KITLG | |||
autosomal dominant nonsyndromic deafness 69 | |||
Waardenburg syndrome |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
decreased ear pigmentation |
increased ear pigmentation |
|
Availability | Mouse Genotype | |||
KitlSl-1Neu/KitlSl-1Neu | ||||
KitlSl-3Neu/KitlSl-3Neu | ||||
KitlSl-21J/Kitl+ | ||||
KitlSl-22J/Kitl+ | * |
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 04/30/2024 MGI 6.23 |
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