CCDC22

This gene encodes a protein containing a coiled-coil domain. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. Localization of the orthologous rat protein suggests that it may play a role in neuronal injury response. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2011]

Description

coiled-coil domain containing 22

Protein family

-

Chromosome

X:p11.23 (49091927 - 49106987)

Ensembl ID

ENSG00000101997  (ver. 69.37)

Orthologs

Mouse Ccdc22: ENSMUSG00000031143

Human splice variants
Mouse splice variants