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 |
|---|---|---|---|---|---|---|
| 48482 | Human | SPTBN2 |
HGNC:11276 (HGNC) 6712 (Entrez Gene) 604985 (OMIM) |
11q13.2 | 11: 66682495-66729360 (-) Reference GRCh38.p13 Primary Assembly(NC_000011.10) |
Spinocerebellar ataxia, autosomal recessive 14 (MIM 615386) Spinocerebellar ataxia 5 (MIM 600224) |
| 48482 | Dog | SPTBN2 |
483706 (Entrez Gene) |
- | 18: 49240572-49279277 (+) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006600.4) |
Ataxia |
| 48482 | Mouse | Sptbn2 |
20743 (Entrez Gene) ENSMUSG00000067889 (Ensembl) |
19_A|19_4.1_cM | 19: 4761235-4804005 (+) Reference GRCm39 C57BL/6J(NC_000085.7) |
|
| 48482 | Rat | Sptbn2 |
29211 (Entrez Gene) ENSRNOG00000058842 (Ensembl) |
1q43 | 1: 202002969-202045342 (+) Reference mRatBN7.2 Primary Assembly(NC_051336.1) |
|
| 48482 | Xenopus | sptbn2 |
100486199 (Entrez Gene) ENSXETG00000011850 (Ensembl) |
- | 4: 39033741-39131167 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030680.2) |
|
| 48482 | Macaque | SPTBN2 |
713419 (Entrez Gene) ENSMMUG00000020359 (Ensembl) |
- | 14: 7820081-7865208 (+) Reference Mmul 10 Primary Assembly(NC_041767.1) |
|
| 48482 | Chimpanzee | SPTBN2 |
451353 (Entrez Gene) ENSPTRG00000003936 (Ensembl) |
- | 11: 62644128-62688234 (-) Reference Clint PTRv2 Primary Assembly(NC_036890.1) |