Sequence Detail

ID/Version

Q8BFU8 (UniProt | EBI)

Last sequence update: 2003-03-01
Last annotation update: 2024-01-24

Sequence description from provider

RecName: Full=Vesicular glutamate transporter 3 {ECO:0000303|PubMed:12384506}; Short=VGluT3 {ECO:0000303|PubMed:12384506};AltName: Full=Solute carrier family 17 member 8;

Provider

SWISS-PROT

Sequence

Polypeptide 601 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	Slc17a8	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8	51	105	3	18

Sequence references in MGI

J:91392 Schafer MK, et al., Molecular cloning and functional identification of mouse vesicular glutamate transporter 3 and its expression in subsets of novel excitatory neurons. J Biol Chem. 2002 Dec 27;277(52):50734-48
J:132704 Seal RP, et al., Sensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3. Neuron. 2008 Jan 24;57(2):263-75
J:135586 Gras C, et al., The vesicular glutamate transporter VGLUT3 synergizes striatal acetylcholine tone. Nat Neurosci. 2008 Mar;11(3):292-300
J:139493 Ruel J, et al., Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice. Am J Hum Genet. 2008 Aug;83(2):278-92
J:322974 Mackenzie B, et al., Analysis of a vesicular glutamate transporter (VGLUT2) supports a cell-leakage mode in addition to vesicular packaging. Neurochem Res. 2008 Feb;33(2):238-47