OMIA:000202-143630 : Coat colour, oculocutaneous albinism type I (OCA1), TYR-related in Paroedura picta |
In other species: domestic cat , taurine cattle , dog , rabbit , water buffalo , ass , Japanese medaka , American mink , humpback whale , domestic ferret , pig , domestic guinea pig , Tufted capuchin , dark-spotted frog , Japanese wrinkled frog , Rice frog , lion , Mongolian gerbil , red fox , hamadryas baboon , red deer , Japanese raccoon dog , Japanese ratsnake , golden hamster
Categories: Pigmentation phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 203100 (trait) , 606952 (trait) , 606933 (gene)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: unknown
Cross-species summary: Congenital lack of pigment in most parts of the body. Due to a non-functional form of the enzyme tyrosinase. Also known as Oculocutaneous albinism (OCA), Acromelanism and as the Himalayan coat-colour pattern
Species-specific description: This phene includes references to studies involving gene edited or genetically modified organisms (GMO).
Reference
2023 | Abe, T., Kaneko, M., Kiyonari, H. : |
A reverse genetic approach in geckos with the CRISPR/Cas9 system by oocyte microinjection. Dev Biol :, 2023. Pubmed reference: 36868446 . DOI: 10.1016/j.ydbio.2023.02.005. |
Edit History
- Created by Imke Tammen2 on 09 Mar 2023