Abstract
Severe combined immunodeficiency disease (SCID) of horses is an autosomal, recessive hereditary disease occurring among Arabian horses. The genetic defect responsible for this disease was recently identified as a 5-basepair deletion in the gene encoding DNA-protein kinase catalytic subunit (DNA-PKcs). Horses with one copy of the gene appear normal, while horses with two copies of the gene manifest the disease. The present report describes a PCR-based test for detection of the gene defect and the results from testing 250 randomly selected Arabian horses. The frequency of SCID gene carriers was 8.4% (21/250). Based on the gene frequency reported here, the authors would expect 0.18% (1 out of 567) of Arabian foals to be affected with SCID based on a random breeding population.
| Original language | English |
|---|---|
| Pages (from-to) | 41-42 |
| Number of pages | 2 |
| Journal | Animal Genetics |
| Volume | 29 |
| Issue number | 1 |
| DOIs | |
| State | Published - Feb 1998 |
Keywords
- Gene defect
- Hereditary disease
- Immunodeficiency
- SCID
ASJC Scopus subject areas
- Animal Science and Zoology
- Genetics
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