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 |
|---|---|---|---|---|---|---|
| 4626 | Human | MERTK |
HGNC:7027 (HGNC) 10461 (Entrez Gene) 604705 (OMIM) |
2q13 | 2: 111898606-112029560 (+) Reference GRCh38.p13 Primary Assembly(NC_000002.12) |
Retinitis pigmentosa 38 (MIM 613862) |
| 4626 | Dog | MERTK |
483060 (Entrez Gene) |
- | 17: 36106596-36218037 (+) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006599.4) |
Progressive retinal atrophy (Rod-cone dysplasia) |
| 4626 | Cow | MERTK |
504429 (Entrez Gene) ENSBTAG00000005828 (Ensembl) |
- | 11: 380815-516593 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037338.1) |
|
| 4626 | Mouse | Mertk |
17289 (Entrez Gene) ENSMUSG00000014361 (Ensembl) |
2|2_F1 | 2: 128540834-128645081 (+) Reference GRCm39 C57BL/6J(NC_000068.8) |
|
| 4626 | Rat | Mertk |
65037 (Entrez Gene) ENSRNOG00000017319 (Ensembl) |
3q36 | 3: 115939350-116045140 (+) Reference mRatBN7.2 Primary Assembly(NC_051338.1) |
|
| 4626 | Zebrafish | mertka |
100322133 (Entrez Gene) ENSDARG00000074695 (Ensembl) |
- | 13: 47624162-47689605 (+) Reference GRCz11 Primary Assembly(NC_007124.7) |
|
| 4626 | Xenopus | mertk |
100485743 (Entrez Gene) ENSXETG00000013767 (Ensembl) |
- | 5: 38418708-38475080 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030681.2) |
|
| 4626 | Chicken | MERTK |
395836 (Entrez Gene) ENSGALG00000008257 (Ensembl) |
- | 3: 3378867-3399906 (+) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052534.1) |
|
| 4626 | Macaque | MERTK |
698330 (Entrez Gene) ENSMMUG00000010066 (Ensembl) |
- | 13: 15115926-15252510 (+) Reference Mmul 10 Primary Assembly(NC_041766.1) |
|
| 4626 | Chimpanzee | MERTK |
459492 (Entrez Gene) ENSPTRG00000012358 (Ensembl) |
- | 2A: 91382325-91514505 (-) Reference Clint PTRv2 Primary Assembly(NC_036880.1) |