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)