Version 5.4
Mus musculus Gene: Wbscr22
Summary
InnateDB Gene IDBG-203433.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Wbscr22
Gene Name Williams Beuren syndrome chromosome region 22
Synonyms 1110003N24Rik
Species Mus musculus
Ensembl Gene ENSMUSG00000005378
Encoded Proteins
IDBP-203435
Williams Beuren syndrome chromosome region 22
IDBP-203439
Williams Beuren syndrome chromosome region 22
IDBP-258616
Williams Beuren syndrome chromosome region 22
IDBP-536602
Williams Beuren syndrome chromosome region 22
IDBP-541782
Williams Beuren syndrome chromosome region 22
IDBP-540261
Williams Beuren syndrome chromosome region 22
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 ENSG00000071462:
This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:135052957-135064959
Strand Reverse strand
Band G2
Transcripts
ENSMUST00000071677 ENSMUSP00000071600
ENSMUST00000085984 ENSMUSP00000083146
ENSMUST00000111205 ENSMUSP00000106836
ENSMUST00000129691 ENSMUSP00000120383
ENSMUST00000147756
ENSMUST00000134180
ENSMUST00000151551
ENSMUST00000141765
ENSMUST00000144891
ENSMUST00000149108
ENSMUST00000148549 ENSMUSP00000118370
ENSMUST00000141309 ENSMUSP00000119659
ENSMUST00000129013
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 15 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 15 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0008168 methyltransferase activity
GO:0044822 poly(A) RNA binding
Biological Process
GO:0006364 rRNA processing
GO:0008150 biological_process
GO:0008152 metabolic process
GO:0032259 methylation
Cellular Component
GO:0005575 cellular_component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
ENSG00000071462
View Gene Order
ENSBTAG00000017067
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.439878
RefSeq NM_025375
OMIM
CCDS CCDS19732
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