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GENE INFORMATION

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Gene name

WBSCR17 (HGNC Symbol)

Synonyms

GALNTL3

Description

Williams-Beuren syndrome chromosome region 17 (HGNC Symbol)

Entrez gene summary

This gene encodes an N-acetylgalactosaminyltransferase, which has 97% sequence identity to the mouse protein. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Jul 2008]

Chromosome

7 (Chromosome progress)

Cytoband

q11.22

Chromosome location (bp)

70597155 - 71178585

Ensembl

ENSG00000185274 (version 69.37)

Entrez gene

64409

UniProt

Q6IS24

neXtProt

NX_Q6IS24

Antibodypedia

WBSCR17 antibodies
 

PROTEIN VIEW

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WBSCR17-001
 
WBSCR17-004
 
 
 
 
 

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)

WBSCR17-001 ENSP00000329654
ENST00000333538
Q6IS24
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Show » Show » 598 67.8 No 0
WBSCR17-004 ENSP00000392019
ENST00000447516
H7BZX9
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Show » 188 20.9 No 0