OMIA:000201-9838 : Coat colour, agouti in Camelus dromedarius (Arabian camel)

In other species: gray wolf , coyote , dog , red fox , domestic cat , leopard , ass (donkey) , horse , pig , llama , Western roe deer , impala , taurine cattle , goat , sheep , rabbit , tassel-eared squirrel , North American deer mouse , Mongolian gerbil , meadow voles , domestic guinea pig , alpaca , leopard cat , oldfield mouse , Kodkod , Colocolo , Asiatic golden cat , Northern mole vole , Eurasian water mole

Categories: Pigmentation phene

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 611742 (trait) , 600201 (gene)

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Considered a defect: no

Key variant known: yes

Year key variant first reported: 2018

Cross-species summary: This locus, ASIP, encodes the agouti signalling protein, a peptide antagonist of the melanocyte-stimulating hormone receptor (MC1R), which is the product of the extension locus. As explained by Schneider et al. (PLoS Genet 10(2): e1004892; 2015), "The most common causes of melanism (black coat) mutations are gain-of-function alterations in MC1R, or loss-of function alterations in ASIP, which encodes Agouti signaling protein, a paracrine signaling molecule that inhibits MC1R signaling".

Molecular basis: Adopting the comparative candidate gene approach, Almathen et al. (2018) sequenced the ASIP gene in "91 animals from ten Arabian camel populations, that included the four predominant coat color phenotypes observed in the dromedary (light brown, dark brown, black and white)". They identified two variants "a 1-bp deletion (23delT/T) and a SNP (25G/A) in exon 2 of ASIP" that exist as two haplotypes, namely "23delT-25A and 23T-25G". Noting that the "23delT-25A haplotype results in a frame shift mutation, which changes the amino acid sequence and introduces a premature stop codon at position 24", Almathen et al. (2018) reported that this haplotype is associated with black and dark-brown coat colour: "Animals with black and dark-brown coat colors (n = 40, Magaheem and Sofor [populations]) were homozygous for haplotype 23delT-25A, whereas all light-brown and white individuals (n = 51) were homozygous for the 23T-25G haplotype". Alshanbari et al. (2019) "confirmed that the majority [with 4 exceptions] of black dromedaries were homozygous for . . . [the 23delT-25A] frameshift mutation in ASIP exon 2"

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Associated gene:

Symbol Description Species Chr Location OMIA gene details page Other Links
ASIP agouti signaling protein Camelus dromedarius 18 NC_087453.1 (20192580..20125766) ASIP Homologene, Ensembl , NCBI gene

Variants

By default, variants are sorted chronologically by year of publication, to provide a historical perspective. Readers can re-sort on any column by clicking on the column header. Click it again to sort in a descending order. To create a multiple-field sort, hold down Shift while clicking on the second, third etc relevant column headers.

WARNING! Inclusion of a variant in this table does not automatically mean that it should be used for DNA testing. Anyone contemplating the use of any of these variants for DNA testing should examine critically the relevant evidence (especially in breeds other than the breed in which the variant was first described). If it is decided to proceed, the location and orientation of the variant sequence should be checked very carefully.

Since October 2021, OMIA includes a semiautomated lift-over pipeline to facilitate updates of genomic positions to a recent reference genome position. These changes to genomic positions are not always reflected in the ‘acknowledgements’ or ‘verbal description’ fields in this table.

OMIA Variant ID Breed(s) Variant Phenotype Gene Allele Type of Variant Source of Genetic Variant Reference Sequence Chr. g. or m. c. or n. p. Verbal Description EVA ID Inferred EVA rsID Year Published PubMed ID(s) Acknowledgements
1010 Black and dark-brown coat colour ASIP haplotype Naturally occurring variant c.[23delT;c.25G>A] KU179868; c.[23delT;c.25G>A]. As described by Almathen et al. (2018), this haplotype comprises "a 1-bp deletion (23delT/T) and a SNP (25G/A) in exon 2 of ASIP". 2018 29893870

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2019). OMIA:000201-9838: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

References

Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.

2019 Alshanbari, F., Castaneda, C., Juras, R., Hillhouse, A., Mendoza, M.N., Gutiérrez, G.A., Ponce de León, F.A., Raudsepp, T. :
Comparative FISH-mapping of MC1R, ASIP, and TYRP1 in New and Old World camelids and association analysis with coat color phenotypes in the dromedary (Camelus dromedarius). Front Genet 10:340, 2019. Pubmed reference: 31040864. DOI: 10.3389/fgene.2019.00340.
2018 Almathen, F., Elbir, H., Bahbahani, H., Mwacharo, J., Hanotte, O., Almathen, F., Elbir, H., Bahbahani, H., Mwacharo, J., Hanotte, O. :
Polymorphisms in MC1R and ASIP genes are associated with coat color variation in the Arabian camel. J Hered 109:700-706, 2018. Pubmed reference: 29893870. DOI: 10.1093/jhered/esy024.

Edit History


  • Created by Frank Nicholas on 28 Aug 2018
  • Changed by Frank Nicholas on 28 Aug 2018
  • Changed by Frank Nicholas on 05 Jun 2019