CHRNB2 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	CHRNB2	HGNC:1962 (HGNC) 1141 (Entrez Gene) 118507 (OMIM) CHRNB2 (Alliance of Genome Resources)	Chr1 q21.3	Chr1:154567778-154580013 (+) GRCh38	autosomal dominant nocturnal frontal lobe epilepsy autosomal dominant nocturnal frontal lobe epilepsy 3	P17787 (UniProt \| EBI) NM_000748 (RefSeq)
mouse	Chrnb2	MGI:87891 (MGI) 11444 (Entrez Gene) Gene Tree Chrnb2 (Alliance of Genome Resources)	Chr3 39.19 cM	Chr3:89660755-89671939 (-) GRCm39	attention deficit hyperactivity disorder autism spectrum disorder autosomal dominant nocturnal frontal lobe epilepsy 3	11444 (NCBI Gene Model) Q9ERK7 (UniProt \| EBI) NM_009602 (RefSeq)
rat	Chrnb2	RGD:2350 (Rat Genome Database) 54239 (Entrez Gene) Chrnb2 (Alliance of Genome Resources)	Chr2 q34			P12390 (UniProt \| EBI) NM_019297 (RefSeq)
zebrafish	chrnb2	ZDB-GENE-070821-3 (Zebrafish Model Organism Database) 561906 (Entrez Gene) chrnb2 (Alliance of Genome Resources)	Chr16			XP_005169811 (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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