MYH9 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	MYH9	HGNC:7579 (HGNC) 4627 (Entrez Gene) 160775 (OMIM) MYH9 (Alliance of Genome Resources)	Chr22 q12.3	Chr22:36281280-36388010 (-) GRCh38	autosomal dominant Alport syndrome autosomal dominant nonsyndromic deafness 17 end stage renal disease MYH-9 related disease orofacial cleft proteinuria sensorineural hearing loss thrombocytopenia	P35579 (UniProt \| EBI) NM_002473 (RefSeq)
mouse	Myh9	MGI:107717 (MGI) 17886 (Entrez Gene) Gene Tree Myh9 (Alliance of Genome Resources)	Chr15 36.81 cM	Chr15:77644787-77726375 (-) GRCm39	MYH-9 related disease	ENSMUSG00000022443 (Ensembl Gene Model) ENSMUSP00000016771 (Ensembl) ENSMUST00000016771 (Ensembl)
rat	Myh9	RGD:3140 (Rat Genome Database) 25745 (Entrez Gene) Myh9 (Alliance of Genome Resources)	Chr7 q34			NP_001292806 (RefSeq) NM_001305877 (RefSeq)
zebrafish	myh9b	ZDB-GENE-030131-998 (Zebrafish Model Organism Database) 561431 (Entrez Gene) myh9b (Alliance of Genome Resources)	Chr3			XP_001920098 (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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