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Cat DNA testing illustration

Cystinuria (Type I – A) – Cat

Code: K859

74,72 €

Sample details

One test – one sample. Animal and owner details are optional.

Search by our number or the laboratory number. An unmatched number is saved as a previous / external reference. No new physical sample is needed.
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Short description

Cystinuria is a hereditary renal transport disorder.

General information

Cystinuria is a hereditary renal transport disorder. The disease causes an error of the metabolism, which leads to the formation of cystine crystals and uroliths in the urinary tract. The formation can result in stranguria, hematuria, urinary obstruction and renal failure. The disorder is caused due to a mutation in the solute carrier family 3 (amino acid transporter heavy chain) member 1 (SLC3A1) gene.

Specifications

Breeds

All Breeds
Gene

SLC3A1
Chromosome

A3
Mutation

c.1342C>T
Organ

Respiratory System
Specimen

Swab, Blood EDTA, Blood Heparin, Semen, Tissue
Mode of Inheritance

Autosomal Recessive

Clinical features

Clinical signs include hematuria, dysuria, pollakiuria, urinary obstruction with postrenal failure.

Additional information

This test is based on an association study.

References

Pubmed ID: 25417848

Year published: 2015

Omia ID: 256

Omia variant ID:

Turnaround information

  • 15 working days