ATP13A2 Vertebrate HGNC

Vertebrate Homology

Source

Alliance of Genome Resources

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 select all deselect all Go
human	ATP13A2	HGNC:30213 (HGNC) 23400 (Entrez Gene) 610513 (OMIM) ATP13A2 (Alliance of Genome Resources)	Chr1 p36.13	Chr1:16985958-17011928 (-) GRCh38	hereditary spastic paraplegia 78 Kufor-Rakeb syndrome Parkinson's disease	Q9NQ11 (UniProt \| EBI) NM_001141974 (RefSeq)
mouse	Atp13a2	MGI:1922022 (MGI) 74772 (Entrez Gene) Gene Tree Atp13a2 (Alliance of Genome Resources)	Chr4 73.29 cM	Chr4:140714184-140734641 (+) GRCm39	Kufor-Rakeb syndrome	ENSMUSG00000036622 (Ensembl Gene Model) ENSMUSP00000039648 (Ensembl) ENSMUST00000037055 (Ensembl)
rat	Atp13a2	RGD:1307977 (Rat Genome Database) 362645 (Entrez Gene) Atp13a2 (Alliance of Genome Resources)	Chr5 q36			NP_001166903 (RefSeq) NM_001173432 (RefSeq)
zebrafish	atp13a2	ZDB-GENE-061215-126 (Zebrafish Model Organism Database) 568666 (Entrez Gene) atp13a2 (Alliance of Genome Resources)	Chr23			NP_001073506 (RefSeq) NM_001080037 (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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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