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 |
|---|---|---|---|---|---|---|
| 993 | Human | CNGB1 |
HGNC:2151 (HGNC) 1258 (Entrez Gene) 600724 (OMIM) |
16q21 | 16: 57882339-57971127 (-) Reference GRCh38.p13 Primary Assembly(NC_000016.10) |
Retinitis pigmentosa 45 (MIM 613767) |
| 993 | Dog | CNGB1 |
102156683 (Entrez Gene) |
- | 2: 55204186-55268846 (+) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006584.4) |
Progressive retinal atrophy (Rod-cone dysplasia) |
| 993 | Cow | CNGB1 |
281702 (Entrez Gene) ENSBTAG00000005702 (Ensembl) |
- | 18: 25813829-25882541 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037345.1) |
|
| 993 | Rat | Cngb1 |
83686 (Entrez Gene) ENSRNOG00000031773 (Ensembl) |
19p13 | 19: 9726594-9791110 (+) Reference mRatBN7.2 Primary Assembly(NC_051354.1) |
|
| 993 | Chicken | CNGB1 |
768759 (Entrez Gene) |
- | 11: 445260-460852 (+) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052542.1) |
|
| 993 | Macaque | CNGB1 |
706073 (Entrez Gene) ENSMMUG00000022668 (Ensembl) |
- | 20: 45123160-45229324 (-) Reference Mmul 10 Primary Assembly(NC_041773.1) |
|
| 993 | Chimpanzee | CNGB1 |
454126 (Entrez Gene) ENSPTRG00000008169 (Ensembl) |
- | 16: 42982070-43069971 (-) Reference Clint PTRv2 Primary Assembly(NC_036895.1) |
|
| 136420 | Zebrafish | cngb1a |
568211 (Entrez Gene) ENSDARG00000068242 (Ensembl) |
- | 18: 45456637-45520018 (+) Reference GRCz11 Primary Assembly(NC_007129.7) |
|
| 136420 | Mouse | Cngb1 |
333329 (Entrez Gene) ENSMUSG00000031789 (Ensembl) |
8|8_C5 | 8: 95965670-96033212 (-) Reference GRCm39 C57BL/6J(NC_000074.7) |
|
| 136420 | Xenopus | cngb1 |
100496200 (Entrez Gene) |
- | 4: 75922091-75989460 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030680.2) |