The detail information of Progressive retinal atrophy, CNGA1-related
OMIA Basic Information
Possible human homologues (MIM numbers):
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal Recessive
Considered a defect: yes
Year key mutation first reported: 2015
Species-specific name: -
Species-specific symbol: -
More detail information can see in
Associated Breeds
| iDog Breed Number | Breed Name | Personality | Height | Weight | History | Breed Source |
|---|---|---|---|---|---|---|
| CB216 | Shetland Shepherd Dog | 33-40.6 cm | 6.8-11.3 kg | United Kingdom (Scotland) |
Associated Gene
| Symbol | Description | Species | Position | Other Links |
|---|---|---|---|---|
| CNGA1 | cyclic nucleotide gated channel alpha 1 | Canis lupus familiaris | Chr- : - - - | Homologene, Ensembl, NCBI gene |
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.
| 2015 |
Wiik,A.C.,Ropstad,E.O.,Ekesten,B.,Karlstam,L.,Wade,C.M.,Lingaas,F.: :
Progressive retinal atrophy in Shetland sheepdog is associated with a mutation in the CNGA1 gene. Anim Genet 46:515-21, 2015. Pubmed reference: 26202106 . DOI: 10.1111/age.12323 . |