OMIA:001228-10042 : Spherocytosis in Peromyscus maniculatus (North American deer mouse)

In other species: dog , taurine cattle

Categories: Haematopoietic system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 109270 (gene) , 182900 (trait) , 612653 (trait)

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive

Considered a defect: yes

Key variant known: no

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:001228-10042: 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.

1967 Steinmuller, D., Motulsky, A.G. :
Treatment of hereditary spherocytosis in Peromyscus by radiation and allogeneic bone marrow transplantation. Blood 29:320-30, 1967. Pubmed reference: 5335711.
1963 Fitzpatrick, W.K., Burdette, W.J., Huestis, R.R. :
Cholelithiasis and spherocytosis in Peromyscus. Arch Surg 86:897-903, 1963. Pubmed reference: 13945379.
1960 Anderson, R., Huestis, R.R., Motulsky, A.G. :
Hereditary spherocytosis in the deer mouse. Its similarity to the human disease. Blood 15:491-504, 1960. Pubmed reference: 13793441.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005