Sequence Detail

ID/Version

Q5PT53 Q8BYD0 Q8BV58 Q9CWD6 Q5PT51 (UniProt | EBI)

Last sequence update: 2005-01-04
Last annotation update: 2024-03-27

Sequence description from provider

RecName: Full=Sodium/bile acid cotransporter 7;AltName: Full=Na(+)/bile acid cotransporter 7;AltName: Full=Solute carrier family 10 member 7;

Provider

SWISS-PROT

Sequence

Polypeptide 340 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Slc10a7	solute carrier family 10 (sodium/bile acid cotransporter family), member 7	32	99	3	77

Sequence references in MGI

J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:265027 Dubail J, et al., SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. Nat Commun. 2018 Aug 6;9(1):3087
J:298768 Laugel-Haushalter V, et al., A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta. Front Genet. 2019;10:504