Homo sapiens Gene: CCDC22
Summary
InnateDB Gene IDBG-66074.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CCDC22
Gene Name coiled-coil domain containing 22
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000101997
Encoded Proteins
coiled-coil domain containing 22
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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]
Gene Information
Type Protein coding
Genomic Location Chromosome X:49235467-49250526
Strand Forward strand
Band p11.23
Transcripts
ENST00000376227 ENSP00000365401
ENST00000496651
ENST00000490300
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 14 experimentally validated interaction(s) in this database.
Experimentally validated
Total 14 [view]
Protein-Protein 14 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0005515 protein binding
Biological Process
GO:0008150 biological_process
Cellular Component
GO:0005575 cellular_component
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt O60826
TrEMBL A0A024QZ03
UniProt Splice Variant
Entrez Gene 28952
UniGene Hs.26333
RefSeq NM_014008 XM_005272599
HUGO HGNC:28909
OMIM 300859
CCDS CCDS14322
HPRD 06594
IMGT
EMBL AJ005890 AK291976 BC000972 BC011675 CH471224
GenPept AAH00972 AAH11675 BAF84665 CAA06747 EAW50674 EAW50676
RNA Seq Atlas 28952