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 |
|---|---|---|---|---|---|---|
| 237 | Human | PDE6B |
HGNC:8786 (HGNC) 5158 (Entrez Gene) 180072 (OMIM) |
4p16.3 | 4: 587324-670891 (+) Reference GRCh38.p13 Primary Assembly(NC_000004.12) |
Night blindness, congenital stationary, autosomal dominant 2 (MIM 163500) Retinitis pigmentosa-40 (MIM 613801) |
| 237 | Dog | PDE6B |
399653 (Entrez Gene) |
- | 3: 94212074-94240252 (-) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006585.4) |
Progressive retinal atrophy (Rod-cone dysplasia) Cone-rod dystrophy |
| 237 | Cow | PDE6B |
281974 (Entrez Gene) ENSBTAG00000017480 (Ensembl) |
- | 6: 117653871-117685791 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037333.1) |
|
| 237 | Mouse | Pde6b |
18587 (Entrez Gene) ENSMUSG00000029491 (Ensembl) |
5_F|5_53.07_cM | 5: 108536238-108579608 (+) Reference GRCm39 C57BL/6J(NC_000071.7) |
|
| 237 | Rat | Pde6b |
289878 (Entrez Gene) ENSRNOG00000000065 (Ensembl) |
14p22 | 14: 1323309-1366449 (-) Reference mRatBN7.2 Primary Assembly(NC_051349.1) |
|
| 237 | Xenopus | pde6b |
100487945 (Entrez Gene) ENSXETG00000002736 (Ensembl) |
- | 1: 84232914-84260727 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030677.2) |
|
| 237 | Chicken | PDE6B |
395092 (Entrez Gene) ENSGALG00000015373 (Ensembl) |
- | Z: 54176392-54211782 (-) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052572.1) |
|
| 237 | Macaque | PDE6B |
704196 (Entrez Gene) ENSMMUG00000003282 (Ensembl) |
- | 5: 629508-672386 (+) Reference Mmul 10 Primary Assembly(NC_041758.1) |
|
| 237 | Zebrafish | pde6b |
559332 (Entrez Gene) ENSDARG00000011671 (Ensembl) |
- | 21: 20356440-20376607 (+) Reference GRCz11 Primary Assembly(NC_007132.7) |