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 |
|---|---|---|---|---|---|---|
| 22547 | Human | COL11A2 |
HGNC:2187 (HGNC) 1302 (Entrez Gene) 120290 (OMIM) |
6p21.32 | 6: 33162691-33193008 (-) Reference GRCh38.p13 Primary Assembly(NC_000006.12) |
Deafness, autosomal recessive 53 (MIM 609706) Deafness, autosomal dominant 13 (MIM 601868) Weissenbacher-Zweymuller syndrome (MIM 277610) Stickler syndrome, type III (MIM 184840) Otospondylomegaepiphyseal dysplasia (MIM 215150) Fibrochondrogenesis 2 (MIM 614524) |
| 22547 | Dog | COL11A2 |
481734 (Entrez Gene) |
- | 12: 2707990-2737296 (-) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006594.4) |
Skeletal dysplasia 2 (SD2) |
| 22547 | Cow | COL11A2 |
515435 (Entrez Gene) ENSBTAG00000000601 (Ensembl) |
- | 23: 7349361-7378834 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037350.1) |
|
| 22547 | Mouse | Col11a2 |
12815 (Entrez Gene) ENSMUSG00000024330 (Ensembl) |
17_B1|17_17.98_cM | 17: 34257461-34285658 (+) Reference GRCm39 C57BL/6J(NC_000083.7) |
|
| 22547 | Rat | Col11a2 |
294279 (Entrez Gene) ENSRNOG00000000463|ENSRNOG0000 (Ensembl) |
20p12 | 20: 4786928-4816597 (-) Reference mRatBN7.2 Primary Assembly(NC_051355.1) |
|
| 22547 | Macaque | COL11A2 |
718050 (Entrez Gene) ENSMMUG00000003850 (Ensembl) |
- | 4: 136314073-136343787 (+) Reference Mmul 10 Primary Assembly(NC_041757.1) |
|
| 22547 | Zebrafish | col11a2 |
561679 (Entrez Gene) ENSDARG00000012422 (Ensembl) |
- | 19: 7179741-7225227 (-) Reference GRCz11 Primary Assembly(NC_007130.7) |
|
| 133857 | Xenopus | col11a2 |
448277 (Entrez Gene) ENSXETG00000006510 (Ensembl) |
- | 8: 3794318-3802735 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030684.2) |