Spontaneous mutation in 2310061I04Rik results in reduced expression of mitochondrial genes and impaired brain myelination.

Here, we describe a spontaneous mouse mutant with a deletion in a predicted gene 2310061I04Rik (Rik) of unknown function located on chromosome 17. A 59 base pair long deletion occurred in the first intron of the Rik gene and disrupted its expression. Riknull mice were born healthy and appeared anato...

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Bibliographic Details
Main Authors: Erdyni N Tsitsikov, Khanh P Phan, Yufeng Liu, Alla V Tsytsykova, Rosalia Paterno, David M Sherry, Anthony C Johnson, Ian F Dunn
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2024-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0290487
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