Vertebrate Homology

• Source: Alliance of Genome Resources

Multiple Genome Viewer

Comparative GO Graph (mouse, human, rat)  

Alliance Homology Information

Species	Symbol	Gene Links	Genetic Location	Genome Coordinates (mouse and human only)	Associated Human Diseases	Sequences
human	SCNN1B	HGNC:10600 (HGNC) 6338 (Entrez Gene) 600760 (OMIM) SCNN1B (Alliance of Genome Resources)	Chr16 p12.2	Chr16:23278231-23381294 (+) GRCh38	bronchiectasis 1 Liddle syndrome pseudohypoaldosteronism	P51168 (UniProt | EBI) NM_000336 (RefSeq)
mouse	Scnn1b	MGI:104696 (MGI) 20277 (Entrez Gene) Gene Tree Scnn1b (Alliance of Genome Resources)	Chr7 65.07 cM	Chr7:121464261-121517737 (+) GRCm39	autosomal recessive pseudohypoaldosteronism type 1 cystic fibrosis Liddle syndrome	ENSMUSG00000030873 (Ensembl Gene Model) ENSMUSP00000033161 (Ensembl) ENSMUST00000033161 (Ensembl)
rat	Scnn1b	RGD:3640 (Rat Genome Database) 24767 (Entrez Gene) Scnn1b (Alliance of Genome Resources)	Chr1 q36			P37090 (UniProt | EBI) NM_012648 (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.