Vertebrate Homology

• Source: Alliance of Genome Resources

Multiple Genome Viewer

Comparative GO Graph (mouse, human, rat, zebrafish)  

Alliance Homology Information

Species	Symbol	Gene Links	Genetic Location	Genome Coordinates (mouse and human only)	Associated Human Diseases	Sequences
human	RPGRIP1L	HGNC:29168 (HGNC) 23322 (Entrez Gene) 610937 (OMIM) RPGRIP1L (Alliance of Genome Resources)	Chr16 q12.2	Chr16:53598153-53703938 (-) GRCh38	anencephaly cerebellar ataxia cystic kidney disease intellectual disability Joubert syndrome 7 Meckel syndrome 5 nephronophthisis retinitis pigmentosa 3 vascular dementia	Q68CZ1 (UniProt | EBI) NM_015272 (RefSeq)
mouse	Rpgrip1l	MGI:1920563 (MGI) 244585 (Entrez Gene) Gene Tree Rpgrip1l (Alliance of Genome Resources)	Chr8 44.29 cM	Chr8:91943658-92039890 (-) GRCm39	Joubert syndrome 7 Meckel syndrome	ENSMUSG00000033282 (Ensembl Gene Model) ENSMUSP00000042702 (Ensembl) ENSMUST00000047783 (Ensembl)
rat	Rpgrip1l	RGD:1311099 (Rat Genome Database) 307724 (Entrez Gene) Rpgrip1l (Alliance of Genome Resources)	Chr19 p11			NP_001100884 (RefSeq) NM_001107414 (RefSeq)
zebrafish	rpgrip1l	ZDB-GENE-081104-81 (Zebrafish Model Organism Database) 557688 (Entrez Gene) rpgrip1l (Alliance of Genome Resources)	Chr25			NP_001233589 (RefSeq) NM_001246660 (RefSeq)

Alliance Homology Information

MGI loads orthology data based on the 'stringent' set from the Alliance of Genome Resources. The Alliance sets are based on a scoring system developed by the Alliance in collaboration with DIOPT.

MGI includes orthology for the following vertebrate species from the Alliance:
 - human
 - mouse
 - rat
 - zebrafish

These are a subset of the total species represented in the Alliance; there may be stringent set orthologs in other Alliance species.