Frequency of the SCID gene among Arabian horses in the USA

Authors: Bernoco, D.1; Bailey, E.2

Source: Animal Genetics, Volume 29, Number 1, February 1998 , pp. 41-42(2)

Publisher: Blackwell Publishing

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content

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.

Keywords: immunodeficiency; SCID; hereditary disease; gene defect

Document Type: Research article

DOI: 10.1046/j.1365-2052.1998.00237.x

Affiliations: 1: Stormont Laboratories, Inc., Woodland, CA 95616, USA, 2: M H Gluck Equine Research Center, University of Kentucky, Lexington, KY 40546, USA

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$50.39 plus tax

 

OR

Back to top

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content
Page Help Click here for Page Help
Shopping cart
Tools
Sign in






Need to register?
Sign up here
Text size: A | A | A | A