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15 phene records found |
[show instead gene records] |
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| OMIA ID | Phene | Species Scientific Name | Species Common Name | Gene | Year Key Mutation First Reported | Date Last Modified |
|---|---|---|---|---|---|---|
| OMIA:000185-452646 | Chediak-Higashi syndrome | Neovison vison | American mink | LYST | 2013 | 2013-11-08 |
| OMIA:001274-452646 | Coat colour, black crystal | Neovison vison | American mink | COPA | 2022 | 2022-11-23 |
| OMIA:001249-452646 | Coat colour, brown, TYRP1-related | Neovison vison | American mink | TYRP1 | 2016 | 2020-10-27 |
| OMIA:000031-452646 | Coat colour, dilution, MLPH-related | Neovison vison | American mink | MLPH | 2013 | 2020-06-02 |
| OMIA:002292-452646 | Coat colour, dilution, RAB38-related | Neovison vison | American mink | RAB38 | 2020 | 2020-10-27 |
| OMIA:001680-452646 | Coat colour, dominant white with bilateral deafness | Neovison vison | American mink | MITF | 2019 | 2022-11-15 |
| OMIA:002275-452646 | Coat colour, HPS3-related | Neovison vison | American mink | HPS3 | 2024 | 2024-08-29 |
| OMIA:001889-452646 | Coat colour, talitsa | Neovison vison | American mink | 2013-11-09 | ||
| OMIA:000202-452646 | Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related | Neovison vison | American mink | TYR | 2008 | 2020-06-24 |
| OMIA:000259-452646 | Deafness, generic | Neovison vison | American mink | 2011-11-28 | ||
| OMIA:000327-452646 | Ehlers-Danlos syndrome, generic | Neovison vison | American mink | 2013-11-09 | ||
| OMIA:000449-452646 | Heggedal factor (coat colour) | Neovison vison | American mink | KIT | 2022 | 2024-02-28 |
| OMIA:000679-452646 | Muscular dystrophy | Neovison vison | American mink | 2013-11-09 | ||
| OMIA:000700-452646 | Naked | Neovison vison | American mink | 2013-11-09 | ||
| OMIA:001141-452646 | Tyrosinemia, type II | Neovison vison | American mink | 2013-11-09 |