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GENE INFORMATION

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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 (Chromosome progress)

Cytoband

q11.23

Chromosome location (bp)

73248920 - 73256865

Ensembl

ENSG00000165171 (version 69.37)

Entrez gene

155368

UniProt

Q8N6F8

neXtProt

NX_Q8N6F8

Antibodypedia

WBSCR27 antibodies
 

PROTEIN VIEW

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WBSCR27-001
 
WBSCR27-003
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

WBSCR27-001 ENSP00000297873
ENST00000297873
Q8N6F8
Show all »
Show » 245 26.5 No 0
WBSCR27-003 ENSP00000398533
ENST00000458679
B4DWM3
Show all »
90 9.7 No 0