Version 5.4
Mus musculus Protein: Dpy19l3
Summary
InnateDB Protein IDBP-175050.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Dpy19l3
Protein Name dpy-19-like 3 (C. elegans)
Synonyms
Species Mus musculus
Ensembl Protein ENSMUSP00000054747
InnateDB Gene IDBG-175048 (Dpy19l3)
Protein Structure
UniProt Annotation
Function Probable C-mannosyltransferase that mediates C- mannosylation of tryptophan residues on target proteins. {ECO:0000250}.
Subcellular Localization Membrane {ECO:0000305}; Multi-pass membrane protein {ECO:0000305}.
Disease Associations
Tissue Specificity
Comments
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:0003674 molecular_function
GO:0016757 transferase activity, transferring glycosyl groups
Biological Process
GO:0008150 biological_process
GO:0008152 metabolic process
Cellular Component
GO:0005575 cellular_component
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID MGI:2443952
InterPro IPR018732 Dpy-19
PFAM PF10034
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q71B07
PhosphoSite PhosphoSite-Q71B07
TrEMBL
UniProt Splice Variant
Entrez Gene 233115
UniGene Mm.414309
RefSeq NP_848819
MGI ID
MGI Symbol Dpy19l3
OMIM
CCDS CCDS21155
HPRD
IMGT
EMBL AF538322 AK033395 AK034217 AK045758 BC050065 BC059897
GenPept AAH50065 AAH59897 AAQ10888 BAC28266 BAC28636 BAC32483

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