Mus musculus Protein: Wbscr22
Summary
InnateDB Protein IDBP-203439.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Wbscr22
Protein Name Williams Beuren syndrome chromosome region 22
Synonyms 1110003N24Rik;
Species Mus musculus
Ensembl Protein ENSMUSP00000083146
InnateDB Gene IDBG-203433 (Wbscr22)
Protein Structure
UniProt Annotation
Function S-adenosyl-L-methionine-dependent methyltransferase that specifically methylates the N(7) position of a guanine in 18S rRNA. Important for biogenesis end export of the 40S ribosomal subunit independent on its methyltransferase activity. Locus- specific steroid receptor coactivator. Potentiates transactivation by glucocorticoid (NR3C1), mineralocorticoid (NR3C2), androgen (AR) and progesterone (PGR) receptors. Required for the maintenance of open chromatin at the TSC22D3/GILZ locus to facilitate NR3C1 loading on the response elements. Required for maintenance of dimethylation on histone H3 'Lys-79' (H3K79me2) (By similarity). {ECO:0000250}.
Subcellular Localization Nucleus {ECO:0000250}. Cytoplasm {ECO:0000250}. Note=Localized diffusely throughout the nucleus and the cytoplasm. {ECO:0000250}.
Disease Associations
Tissue Specificity
Comments
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
Protein Structure and Domains
PDB ID MGI:1913388
InterPro IPR013216 Methyltransferase type 11
IPR022238 Uncharacterised protein family, methyltransferase, Williams-Beuren syndrome
IPR029063 S-adenosyl-L-methionine-dependent methyltransferase-like
PFAM PF08241
PF12589
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9CY21
PhosphoSite PhosphoSite-Q9CY21
TrEMBL Q9CV98
UniProt Splice Variant
Entrez Gene 66138
UniGene Mm.439878
RefSeq NP_079651
MGI ID
MGI Symbol Wbscr22
OMIM
CCDS CCDS19732
HPRD
IMGT
EMBL AC084109 AF412035 AK008966 AK011005 AK151986 BC093484 BC117987 CH466529
GenPept AAH93484 AAI17988 AAM62317 BAB25995 BAB27324 BAE30852 EDL19393