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 |
---|---|---|---|---|---|---|
49516 | Human | VPS13B |
HGNC:2183 (HGNC) 157680 (Entrez Gene) 607817 (OMIM) |
8q22.2 | 8: 99013273-99877579 (+) Reference GRCh38.p13 Primary Assembly(NC_000008.11) |
Cohen syndrome (MIM 216550) |
49516 | Dog | VPS13B |
481981 (Entrez Gene) |
- | 13: 1096681-1830491 (+) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006595.4) |
Trapped Neutrophil Syndrome |
49516 | Cow | VPS13B |
512656 (Entrez Gene) ENSBTAG00000012357 (Ensembl) |
- | 14: 64453294-65259451 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037341.1) |
|
49516 | Mouse | Vps13b |
666173 (Entrez Gene) ENSMUSG00000037646 (Ensembl) |
15|15_B3.1 | 15: 35371263-35931374 (+) Reference GRCm39 C57BL/6J(NC_000081.7) |
|
49516 | Rat | Vps13b |
315036 (Entrez Gene) ENSRNOG00000055234 (Ensembl) |
7q22 | 7: 66557861-67128428 (+) Reference mRatBN7.2 Primary Assembly(NC_051342.1) |
|
49516 | Xenopus | vps13b |
100490880 (Entrez Gene) ENSXETG00000007944 (Ensembl) |
- | 6: 128373661-128881686 (-) Reference UCB Xtro 10.0 Primary Assembly(NC_030682.2) |
|
49516 | Chicken | VPS13B |
420242 (Entrez Gene) |
- | 2: 127462267-127873898 (+) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052533.1) |
|
49516 | Macaque | VPS13B |
704477 (Entrez Gene) ENSMMUG00000022186 (Ensembl) |
- | 8: 99285825-100148595 (+) Reference Mmul 10 Primary Assembly(NC_041761.1) |
|
49516 | Chimpanzee | VPS13B |
740973 (Entrez Gene) |
- | 8: 96951746-97812994 (+) Reference Clint PTRv2 Primary Assembly(NC_036887.1) |