Bos taurus Gene: WBSCR16
Summary
InnateDB Gene IDBG-639863.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WBSCR16
Gene Name Williams-Beuren syndrome chromosomal region 16 protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000011753
Encoded Proteins
Williams-Beuren syndrome chromosome region 16
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 null:
This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 25:33178161-33201942
Strand Reverse strand
Band
Transcripts
ENSBTAT00000015608 ENSBTAP00000015608
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 7 interaction(s) predicted by orthology.
Predicted by orthology
Total 7 [view]
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
Cellular Component
GO:0005739 mitochondrion
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL E1BIS5
UniProt Splice Variant
Entrez Gene 513273
UniGene Bt.1520
RefSeq NM_001192346
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02058190
GenPept
RNA Seq Atlas 513273