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Coat colour in alpacas is controlled by a wide range of different genes working together often referred to as “loci”.
10 días laborables
Only available in bundles
Especificaciones
| Breeds | |
|---|---|
| Gene | |
| Chromosome | 19 |
| Mutation | c.292C>T |
| Mode of Inheritance | Autosómico recesivo |
| Organ | |
| Specimen | Hisopo |
| Also known as | A-Locus |
Información específica de la prueba
Coat colour in alpacas is controlled by a wide range of different genes working together often referred to as “loci”. One of the two main loci responsible for base colour is the Agouti locus (A-locus). The A-locus contains the Agouti Signalling Protein (ASIP) gene, which regulates the distribution and balance of the two key pigments in the coat: eumelanin (black/brown pigment) and phaeomelanin (red/yellow pigment). By influencing how and where these pigments are deposited in the hair, ASIP plays a central role in determining an alpaca’s base colour and pattern.
ASIP interacts with the melanocortin 1 receptor (MC1R), also known as the E-locus. Variations at both loci contribute to the diversity of coat colours seen in alpacas. Together, MC1R and ASIP influence whether more dark or light pigment is produced.
There are three mutations in the A-locus associated coat colour variations. This test specifically detects the a2 allele (c.292C>T)
Características clínicas
The A-locus plays a crucial role in producing various coat patterns, contributing to the diversity of coat colours and patterns observed in alpacas. The A-locus influences where on the hair and body each of the two pigments is expressed. A mutation in the A-locus typically causes a darker coat colour. However, overall coat colour is also dependent on other factors like the E-locus and Classic Grey.
Información adicional
Coat colour is an intricate trait that involves a combination of multiple different genes. Testing for a range of different loci will give the most complete prediction of an alpacas coat colour genetics.
Referencias
Pubmed ID: 23558248
Year published: 2013
Omia ID: 201
Omia variant ID: 0