Vertebrate Homology

• Source: Alliance of Genome Resources

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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_001308334 (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_001421365 (RefSeq) NM_001434436 (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.

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