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 |
---|---|---|---|---|---|---|
19131 | Human | FAM161A |
HGNC:25808 (HGNC) 84140 (Entrez Gene) 613596 (OMIM) |
2p15 | 2: 61800239-61854125 (-) Reference GRCh38.p13 Primary Assembly(NC_000002.12) |
Retinitis pigmentosa 28 (MIM 606068) |
19131 | Dog | FAM161A |
100855510 (Entrez Gene) |
- | 10: 61664678-61729583 (-) Alternate Dog10K Boxer Tasha Primary Assembly(NC_006592.4) |
Progressive retinal atrophy (Rod-cone dysplasia) |
19131 | Cow | FAM161A |
532883 (Entrez Gene) |
- | 11: 60420856-60449705 (-) Reference ARS-UCD1.2 Primary Assembly(NC_037338.1) |
|
19131 | Mouse | Fam161a |
73873 (Entrez Gene) ENSMUSG00000049811 (Ensembl) |
11|11_A3.2 | 11: 22956723-22995742 (+) Reference GRCm39 C57BL/6J(NC_000077.7) |
|
19131 | Rat | Fam161a |
289833 (Entrez Gene) ENSRNOG00000009881 (Ensembl) |
14q22 | 14: 97009448-97027864 (+) Reference mRatBN7.2 Primary Assembly(NC_051349.1) |
|
19131 | Xenopus | fam161a |
100144951 (Entrez Gene) ENSXETG00000010466 (Ensembl) |
- | 5: 33456654-33464950 (+) Reference UCB Xtro 10.0 Primary Assembly(NC_030681.2) |
|
19131 | Chicken | FAM161A |
769188 (Entrez Gene) ENSGALG00000008810 (Ensembl) |
- | 3: 15039583-15048278 (+) Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052534.1) |
|
19131 | Macaque | FAM161A |
719626 (Entrez Gene) ENSMMUG00000013972 (Ensembl) |
- | 13: 46915183-46946212 (+) Reference Mmul 10 Primary Assembly(NC_041766.1) |
|
19131 | Chimpanzee | FAM161A |
459265 (Entrez Gene) ENSPTRG00000011964 (Ensembl) |
- | 2A: 61926940-61991500 (-) Reference Clint PTRv2 Primary Assembly(NC_036880.1) |
|
19131 | Zebrafish | fam161a |
558320 (Entrez Gene) ENSDARG00000089742 (Ensembl) |
- | 1: 53686826-53701665 (-) Reference GRCz11 Primary Assembly(NC_007112.7) |