OMIA 002426-10042 : Coat colour, dominant spot in Peromyscus maniculatus
Mendelian trait/disorder: yes Mode of inheritance: Autosomal Dominant Considered a defect: yes Key variant known: no Inheritance: S/S homozygotes are likely embryonic lethal Mapping: Shang et al. (2020) "conduct a candidate gene linkage analysis for the Dominant spot trait and determined that Dominant spot is linked to a region of chromosome 20 that contains a strong candidate gene, Sox10. During the linkage analysis, we found that the spot size varied quantitively in affected Peromyscus based on genetic background."
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.
|2020||Shang, Z., Horovitz, D.J., McKenzie, R.H., Keisler, J.L., Felder, M.R., Davis, S.W. :|
|Using genomic resources for linkage analysis in Peromyscus with an application for characterizing Dominant Spot. BMC Genomics 21:622, 2020. Pubmed reference: 32912160. DOI: 10.1186/s12864-020-06969-1.|
|2013||Vrana, P.B., Shorter, K.R., Szalai, G., Felder, M.R., Crossland, J.P., Veres, M., Allen, J.E., Wiley, C.D., Duselis, A.R., Dewey, M.J., Dawson, W.D. :|
|Peromyscus (deer mice) as developmental models. Wiley Interdiscip Rev Dev Biol 3:211-30, 2013. Pubmed reference: 24896658. DOI: 10.1002/wdev.132.|
|1936||Feldman, H.W. :|
|Piebald characters of the deer mouse. J Heredity 27:301, 1936.|
- Created by Imke Tammen2 on 16 Sep 2021
- Changed by Imke Tammen2 on 16 Sep 2021