Expression of WBSCR27 in cancer - Summary

CANCER ATLAS

Gene description

Williams Beuren syndrome chromosome region 27

Protein class

Disease related genes, Predicted intracellular proteins

Protein evidence

Evidence at protein level

Colorectal cancer

Breast cancer

Prostate cancer

Lung cancer

Liver cancer

STAINING SUMMARY

HPA022420

GENE INFORMATION
Gene name	WBSCR27
Synonyms
Description	Williams Beuren syndrome chromosome region 27 (HGNC Symbol)
Entrez gene summary	This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]
Chromosome	7
Cytoband	q11.23
Chromosome location (bp)	73834590 - 73842535
Protein evidence	Evidence at protein level (all genes)
Ensembl	ENSG00000165171 (version 83.38)
Entrez gene	155368
UniProt	Q8N6F8 (UniProt - Evidence at protein level)
neXtProt	NX_Q8N6F8
Antibodypedia	WBSCR27 antibodies

PROTEIN BROWSER

WBSCR27-001

PROTEIN INFORMATION
Splice variant	UniProt	Protein class	Gene ontology	Length & mass	Signal peptide (predicted)	Transmembrane regions (predicted)
WBSCR27-001 ENSP00000297873 ENST00000297873	Q8N6F8 [Direct mapping] Williams-Beuren syndrome chromosomal region 27 protein Show all	Predicted intracellular proteins Disease related genes Show all	GO:0005515 [protein binding] GO:0008757 [S-adenosylmethionine-dependent methyltransferase activity] GO:0032259 [methylation] Show all	245 aa 26.5 kDa	No	0