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OMIA:002331-9986 : Cardiomyopathy, TNNI3-related in Oryctolagus cuniculus (rabbit)

Categories: Cardiovascular system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 613286 (trait) , 115210 (trait) , 613690 (trait) , 611880 (trait)

Mendelian trait/disorder: yes

Disease-related: yes

Key variant known: no

Inheritance: Transgenic model of human disease (GMO)

Genetic engineering: Yes - variants have been created artificially, e.g. by genetic engineering or gene editing
Have human generated variants been created, e.g. through genetic engineering and gene editing

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2024). OMIA:002331-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

References

Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.

2022 Hornyik, T., Rieder, M., Castiglione, A., Major, P., Baczko, I., Brunner, M., Koren, G., Odening, K.E. :
Transgenic rabbit models for cardiac disease research. Br J Pharmacol 179:938-957, 2022. Pubmed reference: 33822374. DOI: 10.1111/bph.15484.
2005 Sanbe, A., James, J., Tuzcu, V., Nas, S., Martin, L., Gulick, J., Osinska, H., Sakthivel, S., Klevitsky, R., Ginsburg, K.S., Bers, D.M., Zinman, B., Lakatta, E.G., Robbins, J. :
Transgenic rabbit model for human troponin I-based hypertrophic cardiomyopathy. Circulation 111:2330-8, 2005. Pubmed reference: 15867176. DOI: 10.1161/01.CIR.0000164234.24957.75.

Edit History


  • Created by Imke Tammen2 on 21 Apr 2021
  • Changed by Imke Tammen2 on 18 Oct 2024