OMIA:002130-8081 : Oculocutaneous albinism, OCA2-related in Poecilia reticulata (guppy) |
In other species: Mexican tetra , Rhesus monkey , dog , pig , corn snake
Categories: Pigmentation phene
Links to possible relevant human trait(s) and/or gene(s) in OMIM: 203200 (trait) , 611409 (gene)
Links to relevant human diseases in MONDO:
Mendelian trait/disorder: unknown
Disease-related: no
Cross-species summary: Tyrosinase-positive oculocutaneous albinism (OCA, type II) is an autosomal recessive disorder in which the biosynthesis of melanin pigment is reduced in skin, hair, and eyes. Renamed from 'Coat colour, oculocutaneous albinism, OCA2-related' [07/09/2024]
Species-specific name: Red eye colour
Species-specific description: Chang et al. (2024) "use genomic and transcriptomic analyses to identify candidate genes and propose that OCA2 is the most important candidate gene for the red-eyed phenotype in domestic guppies."
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2024). OMIA:002130-8081: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2024 | Chang, Y., Wu, S., Li, J., Bao, H., Wu, C. : |
| Identification of candidate genes for red-eyed (albinism) domestic guppies using genomic and transcriptomic analyses. Int J Mol Sci 25:2175, 2024. Pubmed reference: 38396851. DOI: 10.3390/ijms25042175. |
Edit History
- Created by Imke Tammen2 on 07 Sep 2024
- Changed by Imke Tammen2 on 07 Sep 2024