RAPSN 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	RAPSN	HGNC:9863 (HGNC) 5913 (Entrez Gene) 601592 (OMIM) RAPSN (Alliance of Genome Resources)	Chr11 p11.2	Chr11:47437764-47449143 (-) GRCh38	congenital myasthenic syndrome 11 fetal akinesia deformation sequence syndrome 2	Q13702 (UniProt \| EBI) NM_005055 (RefSeq)
mouse	Rapsn	MGI:99422 (MGI) 19400 (Entrez Gene) Gene Tree Rapsn (Alliance of Genome Resources)	Chr2 50.44 cM	Chr2:90865965-90876074 (+) GRCm39	congenital myasthenic syndrome 11	ENSMUSG00000002104 (Ensembl Gene Model) ENSMUSP00000054150 (Ensembl) ENSMUST00000050323 (Ensembl)
rat	Rapsn	RGD:1311592 (Rat Genome Database) 362161 (Entrez Gene) Rapsn (Alliance of Genome Resources)	Chr3 q24			NP_001102054 (RefSeq) NM_001108584 (RefSeq)
zebrafish	rapsn	ZDB-GENE-030313-1 (Zebrafish Model Organism Database) 352942 (Entrez Gene) rapsn (Alliance of Genome Resources)	Chr18			NP_840090 (RefSeq) NM_178305 (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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