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 |
|---|---|---|---|---|---|---|
| 55455 | Human | RPGR |
HGNC:10295 (HGNC) 6103 (Entrez Gene) 312610 (OMIM) |
Xp11.4 | X: 38269162-38327508 (-) Reference GRCh38.p13 Primary Assembly(NC_000023.11) |
Leber congenital amaurosis 6 (MIM 613826) Cone-rod dystrophy 13 (MIM 608194) COACH syndrome (MIM 216360) Meckel syndrome 5 (MIM 611561) Joubert syndrome 7 (MIM 611560) Cone-rod dystrophy, X-linked, 1 (MIM 304020) Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness (MIM 300455) Retinitis pigmentosa 3 (MIM 300029) Macular degeneration, X-linked atrophic (MIM 300834) |
| 55455 | Dog | RPGR |
403726 (Entrez Gene) |
- | X: 20405035-20453689 (-) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006621.4) |
Progressive retinal atrophy (Rod-cone dysplasia) |
| 10679 | Cow | RPGRIP1 |
282656 (Entrez Gene) ENSBTAG00000004694 (Ensembl) |
- | 10: 25806089-25862324 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037337.1) |
|
| 10679 | Mouse | Rpgrip1 |
77945 (Entrez Gene) ENSMUSG00000057132 (Ensembl) |
14|14_C2 | 14: 52341697-52398795 (+) Reference GRCm39 C57BL/6J(NC_000080.7) |
|
| 10679 | Rat | Rpgrip1 |
305850 (Entrez Gene) ENSRNOG00000011809 (Ensembl) |
15p14 | 15: 24814575-24867521 (+) Reference mRatBN7.2 Primary Assembly(NC_051350.1) |
|
| 10679 | Xenopus | rpgrip1 |
100497908 (Entrez Gene) ENSXETG00000006702 (Ensembl) |
- | 1: 142091761-142113863 (-) Reference UCB Xtro 10.0 Primary Assembly(NC_030677.2) |
|
| 10679 | Macaque | RPGRIP1 |
707961 (Entrez Gene) ENSMMUG00000021552 (Ensembl) |
- | 7: 83188903-83252519 (+) Reference Mmul 10 Primary Assembly(NC_041760.1) |
|
| 10679 | Chimpanzee | RPGRIP1 |
473331 (Entrez Gene) ENSPTRG00000006120 (Ensembl) |
- | 14: 2219446-2276040 (+) Reference Clint PTRv2 Primary Assembly(NC_036893.1) |
|
| 18296 | Cow | RPGRIP1L |
518659 (Entrez Gene) ENSBTAG00000012499 (Ensembl) |
- | 18: 21941759-22040310 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037345.1) |
|
| 18296 | Mouse | Rpgrip1l |
244585 (Entrez Gene) ENSMUSG00000033282 (Ensembl) |
8_C5|8_44.29_cM | 8: 91943657-92039918 (-) Reference GRCm39 C57BL/6J(NC_000074.7) |
|
| 18296 | Rat | Rpgrip1l |
307724 (Entrez Gene) ENSRNOG00000011829 (Ensembl) |
19p11 | 19: 15692188-15785082 (+) Reference mRatBN7.2 Primary Assembly(NC_051354.1) |
|
| 18296 | Xenopus | rpgrip1l |
100271765 (Entrez Gene) ENSXETG00000007967 (Ensembl) |
- | 4: 41528851-41608556 (-) Reference UCB Xtro 10.0 Primary Assembly(NC_030680.2) |
|
| 18296 | Chicken | RPGRIP1L |
425392 (Entrez Gene) ENSGALG00000003602 (Ensembl) |
- | 11: 4518000-4581178 (+) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052542.1) |
|
| 18296 | Macaque | RPGRIP1L |
697345 (Entrez Gene) ENSMMUG00000020580 (Ensembl) |
- | 20: 40725435-40824844 (-) Reference Mmul 10 Primary Assembly(NC_041773.1) |
|
| 18296 | Chimpanzee | RPGRIP1L |
454089 (Entrez Gene) ENSPTRG00000008117 (Ensembl) |
- | 16: 38651677-38754363 (-) Reference Clint PTRv2 Primary Assembly(NC_036895.1) |
|
| 18296 | Zebrafish | rpgrip1l |
557688 (Entrez Gene) ENSDARG00000051754 (Ensembl) |
- | 25: 36045071-36081732 (+) Reference GRCz11 Primary Assembly(NC_007136.7) |
|
| 55455 | Mouse | Rpgr |
19893 (Entrez Gene) ENSMUSG00000031174 (Ensembl) |
X|X_A1.1 | X: 10024454-10083033 (-) Reference GRCm39 C57BL/6J(NC_000086.8) |
|
| 55455 | Rat | Rpgr |
367733 (Entrez Gene) ENSRNOG00000003013 (Ensembl) |
Xq12 | X: 12566446-12628170 (+) Reference mRatBN7.2 Primary Assembly(NC_051356.1) |
|
| 55455 | Xenopus | rpgr |
733454 (Entrez Gene) |
- | 2: 58079336-58108551 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030678.2) |
|
| 55455 | Zebrafish | rpgrb |
557752 (Entrez Gene) ENSDARG00000057074 (Ensembl) |
- | 11: 29770869-29790224 (+) Reference GRCz11 Primary Assembly(NC_007122.7) |