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 |
|---|---|---|---|---|---|---|
| 14988 | Human | TTC8 |
HGNC:20087 (HGNC) 123016 (Entrez Gene) 608132 (OMIM) |
14q31.3 | 14: 88824152-88881078 (+) Reference GRCh38.p13 Primary Assembly(NC_000014.9) |
Bardet-Biedl syndrome 8 (MIM 615985) ?Retinitis pigmentosa 51 (MIM 613464) |
| 14988 | Dog | TTC8 |
480413 (Entrez Gene) |
- | 8: 59641065-59693905 (+) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006590.4) |
Progressive Retinal Atrophy |
| 14988 | Zebrafish | ttc8 |
678551 (Entrez Gene) ENSDARG00000099481 (Ensembl) |
- | -: 0-0 (-) - |
|
| 14988 | Cow | TTC8 |
615652 (Entrez Gene) ENSBTAG00000030432 (Ensembl) |
- | 10: 100502973-100562242 (+) Reference ARS-UCD1.2 Primary Assembly(NC_037337.1) |
|
| 14988 | Mouse | Ttc8 |
76260 (Entrez Gene) ENSMUSG00000021013 (Ensembl) |
12|12_E | 12: 98886795-98949508 (+) Reference GRCm39 C57BL/6J(NC_000078.7) |
|
| 14988 | Rat | Ttc8 |
299246 (Entrez Gene) ENSRNOG00000004542 (Ensembl) |
6q32 | 6: 118198185-118252421 (+) Reference mRatBN7.2 Primary Assembly(NC_051341.1) |
|
| 14988 | Xenopus | ttc8 |
733857 (Entrez Gene) ENSXETG00000004396 (Ensembl) |
- | 8: 86090770-86126105 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030684.2) |
|
| 14988 | Chicken | TTC8 |
423401 (Entrez Gene) ENSGALG00000010663 (Ensembl) |
- | 5: 42785556-42822118 (+) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052536.1) |
|
| 14988 | Macaque | TTC8 |
694362 (Entrez Gene) ENSMMUG00000004612 (Ensembl) |
- | 7: 150961284-151016935 (+) Reference Mmul 10 Primary Assembly(NC_041760.1) |
|
| 14988 | Chimpanzee | TTC8 |
467531 (Entrez Gene) ENSPTRG00000006610 (Ensembl) |
- | 14: 69657818-69711884 (+) Reference Clint PTRv2 Primary Assembly(NC_036893.1) |