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 |
---|---|---|---|---|---|---|
466 | Human | VWF |
HGNC:12726 (HGNC) 7450 (Entrez Gene) 613160 (OMIM) |
12p13.31 | 12: 5948876-6124669 (-) Reference GRCh38.p13 Primary Assembly(NC_000012.12) |
von Willibrand disease, type 3 (MIM 277480) von Willebrand disease, types 2A, 2B, 2M, and 2N (MIM 613554) von Willebrand disease, type 1 (MIM 193400) Thrombotic thrombocytopenic purpura, familial (MIM 274150) |
466 | Dog | VWF |
399544 (Entrez Gene) |
- | 27: 7641827-7779173 (-) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006609.4) |
von Willebrand's disease |
466 | Cow | VWF |
280958 (Entrez Gene) ENSBTAG00000012265 (Ensembl) |
- | 5: 104187286-104345682 (+) Reference ARS-UCD1.2 Primary Assembly(NC_037332.1) |
|
466 | Zebrafish | vwf |
570643 (Entrez Gene) ENSDARG00000077231 (Ensembl) |
- | 18: 7146379-7228003 (+) Reference GRCz11 Primary Assembly(NC_007129.7) |
|
466 | Mouse | Vwf |
22371 (Entrez Gene) ENSMUSG00000001930 (Ensembl) |
6_F3|6_59.32_cM | 6: 125529910-125663641 (+) Reference GRCm39 C57BL/6J(NC_000072.7) |
|
466 | Rat | Vwf |
116669 (Entrez Gene) ENSRNOG00000019689 (Ensembl) |
4q42 | 4: 158360151-158491538 (+) Reference mRatBN7.2 Primary Assembly(NC_051339.1) |
|
466 | Xenopus | vwf |
100492314 (Entrez Gene) ENSXETG00000020882 (Ensembl) |
- | 3: 18580748-18695651 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030679.2) |
|
466 | Chicken | VWF |
419031 (Entrez Gene) ENSGALG00000017272 (Ensembl) |
- | 1: 74643817-74782624 (-) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052532.1) |
|
466 | Macaque | VWF |
722019 (Entrez Gene) ENSMMUG00000022893 (Ensembl) |
- | 11: 6082430-6255439 (-) Reference Mmul 10 Primary Assembly(NC_041764.1) |
|
466 | Chimpanzee | VWF |
451773 (Entrez Gene) ENSPTRG00000004566 (Ensembl) |
- | 12: 6140902-6317471 (-) Reference Clint PTRv2 Primary Assembly(NC_036891.1) |