Literature DB >> 16880690

A novel mutant mouse, joggle, with inherited ataxia.

Ziyan Chen1, Shizu Hayasaka, Yoshiko Takagishi, Yoshiharu Murata, Sen-ichi Oda.   

Abstract

While establishing a new mouse strain, we discovered a novel mutant mouse that exhibited ataxia. Mating experiments showed that the mutant phenotype was due to a single autosomal recessive gene, which we have termed joggle (gene symbol: jog). The ataxia becomes apparent around postnatal day 12, when the mice first attempt to walk, and worsens thereafter. The life span of the mutant mouse is comparable to that of the wild-type mouse. After 21 days of age, the cerebellum weights of the jog/jog mice are significantly lower than those of the wild-type mice. These observations indicate that jog/jog mutant mice could be useful models for biomedical research.

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Year:  2006        PMID: 16880690     DOI: 10.1538/expanim.55.411

Source DB:  PubMed          Journal:  Exp Anim        ISSN: 0007-5124


  1 in total

1.  Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.

Authors:  Morag A Lewis; Neil J Ingham; Jing Chen; Selina Pearson; Francesca Di Domenico; Sohinder Rekhi; Rochelle Allen; Matthew Drake; Annelore Willaert; Victoria Rook; Johanna Pass; Thomas Keane; David J Adams; Abigail S Tucker; Jacqueline K White; Karen P Steel
Journal:  BMC Biol       Date:  2022-03-17       Impact factor: 7.431

  1 in total

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