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 |
|---|---|---|---|---|---|---|
| 56940 | Human | ATP13A2 |
HGNC:30213 (HGNC) 23400 (Entrez Gene) 610513 (OMIM) |
1p36.13 | 1: 16985957-17011971 (-) Reference GRCh38.p13 Primary Assembly(NC_000001.11) |
Kufor-Rakeb syndrome (MIM 606693) ?Ceroid lipofuscinosis, neuronal, 12 (MIM 606693) |
| 56940 | Dog | ATP13A2 |
100686975 (Entrez Gene) |
- | 2: 77733474-77752481 (+) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006584.4) |
Neuronal ceroid lipofuscinosis |
| 56940 | Zebrafish | atp13a2 |
568666 (Entrez Gene) ENSDARG00000061890 (Ensembl) |
- | 23: 24511416-24542932 (-) Reference GRCz11 Primary Assembly(NC_007134.7) |
|
| 56940 | Cow | ATP13A2 |
510792 (Entrez Gene) ENSBTAG00000008309 (Ensembl) |
- | 2: 135586338-135606402 (+) Reference ARS-UCD1.2 Primary Assembly(NC_037329.1) |
|
| 56940 | Mouse | Atp13a2 |
74772 (Entrez Gene) ENSMUSG00000036622 (Ensembl) |
4|4_D3 | 4: 140711811-140734640 (+) Reference GRCm39 C57BL/6J(NC_000070.7) |
|
| 56940 | Rat | Atp13a2 |
362645 (Entrez Gene) ENSRNOG00000008052 (Ensembl) |
5q36 | 5: 153292721-153312142 (+) Reference mRatBN7.2 Primary Assembly(NC_051340.1) |
|
| 56940 | Macaque | ATP13A2 |
699678 (Entrez Gene) ENSMMUG00000001610 (Ensembl) |
- | 1: 207752375-207779543 (+) Reference Mmul 10 Primary Assembly(NC_041754.1) |
|
| 56940 | Chimpanzee | ATP13A2 |
456525 (Entrez Gene) ENSPTRG00000000241 (Ensembl) |
- | 1: 15251521-15277583 (-) Reference Clint PTRv2 Primary Assembly(NC_036879.1) |