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 |
|---|---|---|---|---|---|---|
| 11465 | Human | MLPH |
HGNC:29643 (HGNC) 79083 (Entrez Gene) 606526 (OMIM) |
2q37.3 | 2: 237486409-237555321 (+) Reference GRCh38.p13 Primary Assembly(NC_000002.12) |
Griscelli syndrome, type 3 (MIM 609227) |
| 11465 | Dog | MLPH |
607077 (Entrez Gene) |
- | 25: 48618693-48664322 (+) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006607.4) |
Color mutant alopecia |
| 11465 | Cow | MLPH |
531343 (Entrez Gene) ENSBTAG00000000634 (Ensembl) |
- | 3: 116959513-117005442 (+) Reference ARS-UCD1.2 Primary Assembly(NC_037330.1) |
|
| 11465 | Mouse | Mlph |
171531 (Entrez Gene) ENSMUSG00000026303 (Ensembl) |
1_D|1_45.73_cM | 1: 90842749-90878863 (+) Reference GRCm39 C57BL/6J(NC_000067.7) |
|
| 11465 | Rat | Mlph |
316620 (Entrez Gene) ENSRNOG00000019763 (Ensembl) |
9q36 | 9: 91507409-91542983 (+) Reference mRatBN7.2 Primary Assembly(NC_051344.1) |
|
| 11465 | Chimpanzee | MLPH |
460048 (Entrez Gene) ENSPTRG00000013075 (Ensembl) |
- | 2B: 124060148-124125620 (+) Reference Clint PTRv2 Primary Assembly(NC_036881.1) |
|
| 11465 | Zebrafish | mlphb |
557015 (Entrez Gene) ENSDARG00000062481 (Ensembl) |
- | 9: 24008972-24023713 (+) Reference GRCz11 Primary Assembly(NC_007120.7) |
|
| 135668 | Xenopus | mlph |
100145236 (Entrez Gene) ENSXETG00000020907 (Ensembl) |
- | 9: 60405974-60448458 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030685.2) |
|
| 135668 | Chicken | MLPH |
424019 (Entrez Gene) ENSGALG00000003904 (Ensembl) |
- | 7: 4848105-4866995 (-) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052538.1) |
|
| 135668 | Zebrafish | mlpha |
561905 (Entrez Gene) ENSDARG00000070991 (Ensembl) |
- | 6: 15605986-15645443 (-) Reference GRCz11 Primary Assembly(NC_007117.7) |