WBSCR22 Gene Set

Dataset MSigDB Cancer Gene Co-expression Modules
Category transcriptomics
Type co-expressed gene
Description Williams Beuren syndrome chromosome region 22|This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011] (NCBI Entrez Gene Database, 114049)
External Link http://www.broadinstitute.org/gsea/msigdb/cards/CAR_WBSCR22
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36 co-expressed genes for WBSCR22 from the MSigDB Cancer Gene Co-expression Modules dataset.

Symbol Name
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary)
ADRBK1 adrenergic, beta, receptor kinase 1
ATP1B2 ATPase, Na+/K+ transporting, beta 2 polypeptide
CARD10 caspase recruitment domain family, member 10
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
EFNA3 ephrin-A3
IGHMBP2 immunoglobulin mu binding protein 2
IGSF9B immunoglobulin superfamily, member 9B
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
KAT7 K(lysine) acetyltransferase 7
KRT2 keratin 2, type II
KRT33A keratin 33A, type I
KRT86 keratin 86, type II
LY6G6C lymphocyte antigen 6 complex, locus G6C
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MLANA melan-A
NCKIPSD NCK interacting protein with SH3 domain
PCBP3 poly(rC) binding protein 3
PFKFB2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2
POU4F1 POU class 4 homeobox 1
PRSS16 protease, serine, 16 (thymus)
PSG1 pregnancy specific beta-1-glycoprotein 1
PVT1 Pvt1 oncogene (non-protein coding)
RREB1 ras responsive element binding protein 1
SLC12A4 solute carrier family 12 (potassium/chloride transporter), member 4
SLC30A3 solute carrier family 30 (zinc transporter), member 3
ST3GAL2 ST3 beta-galactoside alpha-2,3-sialyltransferase 2
STATH statherin
SULT4A1 sulfotransferase family 4A, member 1
TNP1 transition protein 1 (during histone to protamine replacement)
TRIM58 tripartite motif containing 58
VAMP1 vesicle-associated membrane protein 1 (synaptobrevin 1)
WBSCR22 Williams Beuren syndrome chromosome region 22
WNT10B wingless-type MMTV integration site family, member 10B
ZKSCAN3 zinc finger with KRAB and SCAN domains 3
ZNF157 zinc finger protein 157