Sequence Detail

ID/Version

B2CKC6 (UniProt | EBI)

Last sequence update: 2008-05-20
Last annotation update: 2025-02-05

Sequence description from provider

SubName: Full=EF-hand domain (C-terminal) containing 1 {ECO:0000313|Ensembl:ENSMUSP00000042343.5};SubName: Full=EF-hand domain containing 1 {ECO:0000313|EMBL:ACB20692.1};

Provider

TrEMBL

Sequence

Polypeptide 648 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	Efhc1	EF-hand domain (C-terminal) containing 1	41	104	3	4

Sequence references in MGI

J:145858 Suzuki T, et al., Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility. Hum Mol Genet. 2009 Mar 15;18(6):1099-109
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89