Summary | ||||||||||||||
Mutation origin |
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Mutation description |
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Phenotypes |
View phenotypes and curated references for all genotypes (concatenated display).
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Find Mice (IMSR) |
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Notes |
This mutation was found in the progeny of a neutron-irradiated male at Harwell. Homozygotes and Tyrc-m/Tyrc-ch heterozygotes have patches of chinchilla-type fur and patches of lighter fur similar to that of Tyrc/Tyrc-ch heterozygotes. The two genotypes are distinguishable by the whiter belly of Tyrc-m homozygous mice (J:13502).
Coding regions of the Tyrc-m gene are normal, but upstream sequences are rearranged. Low-level transcription of tyrosinase and reduced sensitivity to DNAase I was found in clones from light pigmenting melanocytes of homozygotes, while in clones from dark pigmenting cells, tyrosinase transcription was higher (though still less than wild-type) and DNAase sensitivity greater. The upstream rearrangement may separate the Tyr structural gene from cis-acting control elements, and the resulting variability of expression cause the light and dark fur patches (J:997).
The triple homozygote Tyrc-m/Tyrc-m Mchm1/Mchm1 Mchm2/Mchm2 is essentially a black-eyed white mouse (J:13834).
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References |
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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 12/10/2024 MGI 6.24 |
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