The homolog information comes from NCBI Homolog. Gene Associated Human Disease comes from NCBI OMIM
| Homolog Group ID | Organism | Symbol | Gene Links | Genetic Location | Genome Coordinates (dog and human only) | Associated Human Diseases |
|---|---|---|---|---|---|---|
| 55432 | Human | CNGA1 |
HGNC:2148 (HGNC) 1259 (Entrez Gene) 123825 (OMIM) |
4p12 | 4: 47935014-48016717 (-) Reference GRCh38.p13 Primary Assembly(NC_000004.12) |
Retinitis pigmentosa 49 (MIM 613756) |
| 55432 | Dog | CNGA1 |
403891 (Entrez Gene) |
- | 13: 43783704-43816817 (-) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006595.4) |
Progressive retinal atrophy (Rod-cone dysplasia) |
| 55432 | Cow | CNGA1 |
281700 (Entrez Gene) ENSBTAG00000002205 (Ensembl) |
- | 6: 66668902-66706868 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037333.1) |
|
| 55432 | Zebrafish | cnga1b |
572249 (Entrez Gene) ENSDARG00000012125 (Ensembl) |
- | 23: 43849132-43866392 (+) Reference GRCz11 Primary Assembly(NC_007134.7) |
|
| 55432 | Mouse | Cnga1 |
12788 (Entrez Gene) ENSMUSG00000067220 (Ensembl) |
5_C3.2|5_38.44_cM | 5: 72761038-72800094 (-) Reference GRCm39 C57BL/6J(NC_000071.7) |
|
| 55432 | Rat | Cnga1 |
85259 (Entrez Gene) ENSRNOG00000004778 (Ensembl) |
14p11 | 14: 35566946-35605064 (+) Reference mRatBN7.2 Primary Assembly(NC_051349.1) |
|
| 55432 | Xenopus | cnga1 |
100491997 (Entrez Gene) |
- | 1: 38738561-38750121 (-) Reference UCB Xtro 10.0 Primary Assembly(NC_030677.2) |
|
| 55432 | Chicken | CNGA1 |
396143 (Entrez Gene) ENSGALG00000014136 (Ensembl) |
- | 4: 66099674-66107160 (+) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052535.1) |
|
| 55432 | Macaque | CNGA1 |
704891 (Entrez Gene) ENSMMUG00000005764 (Ensembl) |
- | 5: 47341429-47360111 (-) Reference Mmul 10 Primary Assembly(NC_041758.1) |
|
| 55432 | Chimpanzee | CNGA1 |
739850 (Entrez Gene) ENSPTRG00000016036|ENSPTRG0000 (Ensembl) |
- | 4: 79357909-79374612 (+) Reference Clint PTRv2 Primary Assembly(NC_036883.1) |