Version 5.4
Mus musculus Gene: Wbscr27
Summary
InnateDB Gene IDBG-203288.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Wbscr27
Gene Name Williams Beuren syndrome chromosome region 27 (human)
Synonyms AW492986; BC002286
Species Mus musculus
Ensembl Gene ENSMUSG00000040557
Encoded Proteins
IDBP-203290
Williams Beuren syndrome chromosome region 27 (human)
IDBP-203292
Williams Beuren syndrome chromosome region 27 (human)
IDBP-258592
Williams Beuren syndrome chromosome region 27 (human)
IDBP-258594
Williams Beuren syndrome chromosome region 27 (human)
IDBP-258596
Williams Beuren syndrome chromosome region 27 (human)
IDBP-541060
Williams Beuren syndrome chromosome region 27 (human)
IDBP-538202
Williams Beuren syndrome chromosome region 27 (human)
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 ENSG00000165171:
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:134932368-134942637
Strand Forward strand
Band G2
Transcripts
ENSMUST00000047196 ENSMUSP00000039080
ENSMUST00000068617 ENSMUSP00000067814
ENSMUST00000111221 ENSMUSP00000106852
ENSMUST00000111219 ENSMUSP00000106850
ENSMUST00000111218 ENSMUSP00000106849
ENSMUST00000136246 ENSMUSP00000119451
ENSMUST00000136815
ENSMUST00000148286 ENSMUSP00000119109
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 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0008168 methyltransferase activity
Biological Process
GO:0008150 biological_process
GO:0008152 metabolic process
GO:0032259 methylation
Cellular Component
GO:0005575 cellular_component
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
ENSG00000165171
View Gene Order
ENSBTAG00000001374
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.34235 Mm.490449
RefSeq NM_024479 XM_006504524 XM_006504530
OMIM
CCDS CCDS19727
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca