Bos taurus Gene: WBSCR17
Summary
InnateDB Gene IDBG-639815.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WBSCR17
Gene Name putative polypeptide N-acetylgalactosaminyltransferase-like protein 3
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000008718
Encoded Proteins
Williams-Beuren syndrome chromosome region 17
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000185274:
This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 25:29391800-29824281
Strand Reverse strand
Band
Transcripts
ENSBTAT00000029707 ENSBTAP00000029705
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0016740 transferase activity
GO:0016757 transferase activity, transferring glycosyl groups
GO:0046872 metal ion binding
Biological Process
GO:0006486 protein glycosylation
Cellular Component
GO:0005794 Golgi apparatus
GO:0016020 membrane
GO:0016021 integral component of membrane
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
O-linked glycosylation of mucins pathway
Post-translational protein modification pathway
O-linked glycosylation pathway
Metabolism of proteins pathway
KEGG
Mucin type O-Glycan biosynthesis pathway
Mucin type O-Glycan biosynthesis pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL E1B9U7
UniProt Splice Variant
Entrez Gene 505622
UniGene Bt.105390 Bt.106149 Bt.12350
RefSeq NM_001192067
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02057963 DAAA02057964 DAAA02057965 DAAA02057966 DAAA02057967 DAAA02057968 DAAA02057969 DAAA02057970 DAAA02057971 DAAA02057972
GenPept
RNA Seq Atlas 505622