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CCDC22


Official Full Name
coiled-coil domain containing 22
Organism
Homo sapiens
Gene ID
28952
Background
This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]
Synonyms
JM1; RTSC2; CXorf37

Cat.No. Product Name Price
SHW009002 shRNA set against Danio rerio CCDC22 (NM_001025485) Inquiry
SHG147679 shRNA set against Mouse Ccdc22(NM_138603.3) Inquiry
SHH256445 shRNA set against Mouse CCDC22 (NM_138603.3) Inquiry
SHH256449 shRNA set against Rat CCDC22 (NM_001135837.1) Inquiry
Cat.No. Product Name Price
CDFR010207 Rat Ccdc22 cDNA Clone(NM_001135837.1) Inquiry
MiUTR1M-02604 CCDC22 miRNA 3'UTR clone Inquiry
MiUTR3H-02950 CCDC22 miRNA 3'UTR clone Inquiry
CDCB158517 Human CCDC22 ORF clone (BC000972) Inquiry
CDCB170477 Danio rerio CCDC22 ORF Clone (NM_001025485) Inquiry
CDCB183397 Rabbit CCDC22 ORF clone (XM_008272610.1) Inquiry
CDCR266138 Mouse Ccdc22 ORF Clone(NM_138603.3) Inquiry
CDCR377250 Rat Ccdc22 ORF Clone(NM_001135837.1) Inquiry
CDCS413462 Human CCDC22 ORF Clone (BC000972) Inquiry
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