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

Categories: Cardiovascular system phene

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 613286 (trait) , 115210 (trait) , 613690 (trait) , 611880 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Considered a defect: yes

Key variant known: no

Inheritance: Transgenic model of human disease (GMO)

Genetic engineering: Unknown
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. (2021). OMIA:002331-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset].


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