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	HSPD1	HGNC:5261 (HGNC) 3329 (Entrez Gene) 118190 (OMIM) HSPD1 (Alliance of Genome Resources)	Chr2 q33.1	Chr2:197486584-197516737 (-) GRCh38	arteriosclerosis autistic disorder coronary artery disease glucose intolerance hereditary spastic paraplegia hereditary spastic paraplegia 13 hypomyelinating leukodystrophy 4	P10809 (UniProt | EBI) NM_199440 (RefSeq)
mouse	Hspd1	MGI:96242 (MGI) 15510 (Entrez Gene) Gene Tree Hspd1 (Alliance of Genome Resources)	Chr1 28.01 cM	Chr1:55116994-55127402 (-) GRCm39	hereditary spastic paraplegia 13	ENSMUSG00000025980 (Ensembl Gene Model) ENSMUSP00000027123 (Ensembl) ENSMUST00000027123 (Ensembl)
rat	Hspd1	RGD:621314 (Rat Genome Database) 63868 (Entrez Gene) Hspd1 (Alliance of Genome Resources)	Chr9 q31			P63039 (UniProt | EBI) NM_022229 (RefSeq)
zebrafish	hspd1	ZDB-GENE-021206-1 (Zebrafish Model Organism Database) 282676 (Entrez Gene) hspd1 (Alliance of Genome Resources)	Chr9			NP_851847 (RefSeq) NM_181330 (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.