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
11325 Human GNGT2 HGNC:4412 (HGNC)
2793 (Entrez Gene)
139391 (OMIM)
17q21.32 17: 49206233-49210573 (-)
Reference GRCh38.p13 Primary Assembly(NC_000017.11)
11325 Dog GNGT2 403617 (Entrez Gene)
- 9: 24829836-24832740 (-)
Alternate Dog10K Boxer Tasha Primary Assembly(NC_006591.4)
Progressive retinal atrophy (Rod-cone dysplasia)
11325 Cow GNGT2 281797 (Entrez Gene)
ENSBTAG00000047325 (Ensembl)
- 19: 37361993-37366299 (+)
Reference ARS-UCD1.2 Primary Assembly(NC_037346.1)
11325 Mouse Gngt2 14710 (Entrez Gene)
ENSMUSG00000038811 (Ensembl)
11_D|11_59.01_cM 11: 95733044-95736556 (+)
Reference GRCm39 C57BL/6J(NC_000077.7)
11325 Rat Gngt2 690825 (Entrez Gene)
ENSRNOG00000006108 (Ensembl)
10q26 10: 80776002-80784234 (+)
Reference mRatBN7.2 Primary Assembly(NC_051345.1)
11325 Zebrafish gngt2a 335655 (Entrez Gene)
ENSDARG00000010680 (Ensembl)
- 3: 23092759-23096134 (+)
Reference GRCz11 Primary Assembly(NC_007114.7)
11325 Xenopus gngt2 100124867 (Entrez Gene)
ENSXETG00000019676 (Ensembl)
- 10: 13887892-13891322 (-)
Reference UCB Xtro 10.0 Primary Assembly(NC_030686.2)
11325 Xenopus gngt2.1 100329130 (Entrez Gene)
ENSXETG00000004704 (Ensembl)
- 2: 78381823-78391752 (+)
Reference UCB Xtro 10.0 Primary Assembly(NC_030678.2)
11325 Chicken GNGT2 100859179 (Entrez Gene)
ENSGALG00000031205 (Ensembl)
- 27: 3248073-3250324 (+)
Reference bGalGal1.mat.broiler.GRCg7b Primary Assembly(NC_052558.1)
11325 Macaque GNGT2 698840 (Entrez Gene)
- 16: 47583902-47588180 (+)
Reference Mmul 10 Primary Assembly(NC_041769.1)
11325 Chimpanzee GNGT2 749133 (Entrez Gene)
ENSPTRG00000009370 (Ensembl)
- 17: 8058696-8066139 (+)
Reference Clint PTRv2 Primary Assembly(NC_036896.1)