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 |
|---|---|---|---|---|---|---|
| 16947 | Human | LOXHD1 |
HGNC:26521 (HGNC) 125336 (Entrez Gene) 613072 (OMIM) |
18q21.1 | 18: 46476960-46657219 (-) Reference GRCh38.p13 Primary Assembly(NC_000018.10) |
Deafness, autosomal recessive 77 (MIM 613079) |
| 16947 | Dog | LOXHD1 |
490467 (Entrez Gene) |
- | 7: 44145777-44310708 (+) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006589.4) |
|
| 16947 | Zebrafish | loxhd1a |
564819 (Entrez Gene) |
- | 21: 5305923-5359960 (+) Reference GRCz11 Primary Assembly(NC_007132.7) |
|
| 16947 | Cow | LOXHD1 |
784983 (Entrez Gene) ENSBTAG00000015210 (Ensembl) |
- | 24: 46187351-46396097 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037351.1) |
|
| 16947 | Zebrafish | loxhd1b |
100150283 (Entrez Gene) ENSDARG00000074638 (Ensembl) |
- | 8: 714622-811049 (-) Reference GRCz11 Primary Assembly(NC_007119.7) |
|
| 16947 | Rat | Loxhd1 |
291427 (Entrez Gene) ENSRNOG00000017410 (Ensembl) |
18q12.3 | 18: 70818275-70969982 (+) Reference mRatBN7.2 Primary Assembly(NC_051353.1) |
|
| 16947 | Xenopus | loxhd1 |
100487617 (Entrez Gene) |
- | 1: 206875261-206974508 (-) Reference UCB Xtro 10.0 Primary Assembly(NC_030677.2) |
|
| 16947 | Chicken | LOXHD1 |
427648 (Entrez Gene) ENSGALG00000037829 (Ensembl) |
- | Z: 2258946-2367977 (+) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052572.1) |
|
| 16947 | Macaque | LOXHD1 |
702221 (Entrez Gene) ENSMMUG00000017246 (Ensembl) |
- | 18: 35794547-35977950 (+) Reference Mmul 10 Primary Assembly(NC_041771.1) |
|
| 16947 | Chimpanzee | LOXHD1 |
455401 (Entrez Gene) ENSPTRG00000009995 (Ensembl) |
- | 18: 40361136-40542340 (-) Reference Clint PTRv2 Primary Assembly(NC_036897.1) |