Homo sapiens Protein: DMWD
Summary
InnateDB Protein IDBP-58110.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DMWD
Protein Name dystrophia myotonica, WD repeat containing
Synonyms D19S593E; DMR-N9; DMRN9; gene59;
Species Homo sapiens
Ensembl Protein ENSP00000270223
InnateDB Gene IDBG-58108 (DMWD)
Protein Structure
UniProt Annotation
Function Could have a regulatory function in meiosis. {ECO:0000269PubMed:8499920}.
Subcellular Localization
Disease Associations
Tissue Specificity Strongest expression in brain, liver, and testis. Also expressed in kidney and spleen.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 38 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 38 [view]
Protein-Protein 38 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0005515 protein binding
Biological Process
Cellular Component
GO:0005575 cellular_component
Protein Structure and Domains
PDB ID
InterPro IPR001680 WD40 repeat
IPR017986 WD40-repeat-containing domain
PFAM PF00400
PRINTS
PIRSF
SMART SM00320
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q09019
PhosphoSite PhosphoSite-Q09019
TrEMBL
UniProt Splice Variant
Entrez Gene 1762
UniGene Hs.515474
RefSeq NP_004934
HUGO HGNC:2936
OMIM 609857
CCDS CCDS33054
HPRD
IMGT
EMBL AC011530 L08835 L19267
GenPept AAA35767 AAC14447