OMIA:000364-9739 : Factor XII deficiency in Tursiops truncatus (bottlenosed dolphin)

In other species: dog , domestic cat , killer whale

Categories: Haematopoietic system phene

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 234000 (trait) , 610619 (gene)

Links to MONDO diseases:

Mendelian trait/disorder: unknown

Considered a defect: yes

Species-specific description: Robinson et al. (1969) reported that factor XII appears to be absent in Atlantic bottlenose dolphins and killer whales.

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. (2011). OMIA:000364-9739: 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.

1969 Lewis, J.H., Bayer, W.L., Szeto, I.L. :
Coagulation factor XII deficiency in the porpoise, Tursiops truncatus. Comp Biochem Physiol 31:667-70, 1969. Pubmed reference: 5367361.
Robinson, A.J., Kropatkin, M., Aggeler, P.M. :
Hageman factor (factor XII) deficiency in marine mammals. Science 166:1420-2, 1969. Pubmed reference: 5388978.

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  • Created by Frank Nicholas on 15 Oct 2011