Crossbred

Albino

The feline albino mutation is a rare mutation that produces a white coat with blue eyes, and is recessive to the sepia and Siamese mutations.

Horse Embryo Pre-Implantation Genetic Diagnosis

Pre-implantation genetic diagnosis (PGD) is a procedure used to screen embryos recovered after uterine flush to determine sex and genetic traits through DNA testing prior to implantation in the uterus.

Tobiano

Tobiano is a white spotting pattern characterized by white on the body that crosses the topline.

Roan Zygosity Test

Roan is a white patterning coat color trait characterized by intermixed white and colored hairs in the body while the head, lower legs, mane, and tail remain colored.

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.

Gray

The gray gene causes progressive depigmentation of the hair, often resulting in a color that is almost completely white by 6-8 years of age. The individual gray test will determine the number of copies of the gray allele (zygosity). The coat color panel tests detect presence or absence of the gray allele.

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.

Cream

Cream is a dilution that causes the palomino, buckskin, smoky black, cremello, perlino, and smoky cream coat colors.

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.

Degenerative Myelopathy (DM)

Degenerative myelopathy (DM) is an inherited neurologic disorder of dogs characterized by gradual muscle wasting and loss of coordination typically beginning in the hind limbs. Testing is most appropriate for those breeds in which the clinical disease has been associated with the SOD1 allele.