Literature DB >> 9682449

Frequency of the SCID gene among Arabian horses in the USA.

D Bernoco1, E Bailey.   

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.

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Year:  1998        PMID: 9682449     DOI: 10.1046/j.1365-2052.1998.00237.x

Source DB:  PubMed          Journal:  Anim Genet        ISSN: 0268-9146            Impact factor:   3.169


  3 in total

Review 1.  Equine clinical genomics: A clinician's primer.

Authors:  M M Brosnahan; S A Brooks; D F Antczak
Journal:  Equine Vet J       Date:  2010-10       Impact factor: 2.888

2.  Whole-genome SNP association in the horse: identification of a deletion in myosin Va responsible for Lavender Foal Syndrome.

Authors:  Samantha A Brooks; Nicole Gabreski; Donald Miller; Abra Brisbin; Helen E Brown; Cassandra Streeter; Jason Mezey; Deborah Cook; Douglas F Antczak
Journal:  PLoS Genet       Date:  2010-04-15       Impact factor: 5.917

3.  Investigation of Known Genetic Mutations of Arabian Horses in Egyptian Arabian Foals with Juvenile Idiopathic Epilepsy.

Authors:  M Aleman; C J Finno; K Weich; M C T Penedo
Journal:  J Vet Intern Med       Date:  2017-11-24       Impact factor: 3.333

  3 in total

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