Pura Raza Menorquina

Polysaccharide Storage Myopathy (PSSM1)

Type 1 Polysaccharide Storage Myopathy is a glycogen storage disease that results in the accumulation of abnormal complex sugars in muscle cells, which can lead to muscle pain, weakness, and reluctance to move.

White Pattern Panel 1

The White Pattern Panel 1 offers diagnostic tests for a variety of white coat color patterns.

Horse Coat Color Panel

The horse coat color panel bundles together several diagnostic tests to evaluate coat color.

SynchroGait (DMRT3)

SynchroGait is a diagnostic DNA test for a genetic variant (A) that has a major impact on the gait and coordination of horses. The discovery by researchers in Sweden showed that the mutation “facilitates lateral gaits, ambling and pace, and inhibits the transition from trot or pace to gallop”. The gait A variant has been identified as a major genetic factor for performance in trotting horses and ability to perform the additional “flying pace” in Icelandic horses. 

Red Factor

The extension gene, or red factor, determines whether a horse will have a chestnut base coat color or a black or bay base coat color.

Dominant White Mutations – W5, W10, W13, W20, and W22

Dominant white is a variable white spotting pattern caused by many different mutations in the KIT gene. The VGL tests for the five most common mutations known as W5, W10, W13, W20, and W22. Homozygosity for W5, W10, W13 or W22 is thought to be non-viable.

Agouti (Bay/Black)

The agouti gene controls the distribution of black pigment, and determines whether a horse will have a bay or black base coat color.