Sequence Detail

ID/Version

E9Q9W7 X4YT46 X4YT42 X4YZM3 E9Q9U9 X4ZGA7 (UniProt | EBI)

Last sequence update: 2012-10-03
Last annotation update: 2024-01-24

Sequence description from provider

RecName: Full=PDZ domain-containing protein 7 {ECO:0000305};

Provider

SWISS-PROT

Sequence

Polypeptide 1021 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	Pdzd7	PDZ domain containing 7	33	96	4	4

Sequence references in MGI

J:209073 Zou J, et al., Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice. Hum Mol Genet. 2014 May 1;23(9):2374-90
J:218667 Chen Q, et al., Whirlin and PDZ domain-containing 7 (PDZD7) proteins are both required to form the quaternary protein complex associated with Usher syndrome type 2. J Biol Chem. 2014 Dec 26;289(52):36070-88
J:236403 Morgan CP, et al., PDZD7-MYO7A complex identified in enriched stereocilia membranes. Elife. 2016 Aug 15;5:e18312
J:266111 Hu QX, et al., Constitutive Galphai coupling activity of very large G protein-coupled receptor 1 (VLGR1) and its regulation by PDZD7 protein. J Biol Chem. 2014 Aug 29;289(35):24215-25
J:266117 Grati M, et al., Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network. J Neurosci. 2012 Oct 10;32(41):14288-93