STOCK MitfRorp/H
Status | Available to order |
EMMA ID | EM:00439 |
International strain name | STOCK MitfRorp/H |
Alternative name | GENA336 |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | MitfRorp, |
Gene/Transgene symbol | Mitf |
Information from provider
Provider | Mary Lyon |
Provider affiliation | MRC Mammalian Genetics Unit |
Phenotypic information | Mice heterozygous for MitfRorp have a diluted coat colour and retinal orange patches. Homozygotes are white with dark eyes. |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Tietz syndrome / Orphanet_42665
- Ocular albinism with congenital sensorineural deafness / Orphanet_352740
- Waardenburg syndrome type 2 / Orphanet_895
- Waardenburg-Shah syndrome / Orphanet_897
MGI phenotypes (allele matching)
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