Sequence Detail

ID/Version

Q6NS45 Q3ULU6 Q8C6T6 Q8C304 (UniProt | EBI)

Last sequence update: 2008-02-26
Last annotation update: 2024-05-29

Sequence description from provider

RecName: Full=Coiled-coil domain-containing protein 66 {ECO:0000305};

Provider

SWISS-PROT

Sequence

Polypeptide 935 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	Ccdc66	coiled-coil domain containing 66	37	98	3	11

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:174954 Gerding WM, et al., Ccdc66 null mutation causes retinal degeneration and dysfunction. Hum Mol Genet. 2011 Sep 15;20(18):3620-31
J:261912 Dekomien G, et al., Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene. Neurogenetics. 2010 May;11(2):163-74
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89