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 |
---|---|---|---|---|---|---|
73874 | Human | COL1A1 |
HGNC:2197 (HGNC) 1277 (Entrez Gene) 120150 (OMIM) |
17q21.33 | 17: 50184095-50201648 (-) Reference GRCh38.p13 Primary Assembly(NC_000017.11) |
Osteogenesis imperfecta, type I (MIM 166200) Ehlers-Danlos syndrome, type VIIA (MIM 130060) {Bone mineral density variation QTL, osteoporosis} (MIM 166710) Ehlers-Danlos syndrome, classic (MIM 130000) Osteogenesis imperfecta, type IV (MIM 166220) Caffey disease (MIM 114000) Osteogenesis imperfecta, type III (MIM 259420) Osteogenesis imperfecta, type II (MIM 166210) |
73874 | Dog | COL1A1 |
403651 (Entrez Gene) |
- | 9: 25576912-25592982 (-) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006591.4) |
Osteogenesis imperfecta |
73874 | Cow | COL1A1 |
282187 (Entrez Gene) ENSBTAG00000013103 (Ensembl) |
- | 19: 36457700-36475646 (+) Reference ARS-UCD1.2 Primary Assembly(NC_037346.1) |
|
73874 | Mouse | Col1a1 |
12842 (Entrez Gene) ENSMUSG00000001506 (Ensembl) |
11_59.01_cM|11_D | 11: 94827049-94843867 (+) Reference GRCm39 C57BL/6J(NC_000077.7) |
|
73874 | Rat | Col1a1 |
29393 (Entrez Gene) ENSRNOG00000003897 (Ensembl) |
10q26 | 10: 79883621-79900624 (+) Reference mRatBN7.2 Primary Assembly(NC_051345.1) |
|
73874 | Xenopus | col1a1 |
496414 (Entrez Gene) ENSXETG00000009031 (Ensembl) |
- | 10: 18236514-18262668 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030686.2) |
|
73874 | Zebrafish | col1a1a |
337158 (Entrez Gene) ENSDARG00000012405 (Ensembl) |
- | 3: 23221173-23237692 (+) Reference GRCz11 Primary Assembly(NC_007114.7) |
|
73874 | Macaque | COL1A1 |
574201 (Entrez Gene) ENSMMUG00000001467 (Ensembl) |
- | 16: 46588740-46606661 (+) Reference Mmul 10 Primary Assembly(NC_041769.1) |