Homo sapiens Gene: DMWD
Summary
InnateDB Gene IDBG-58108.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DMWD
Gene Name dystrophia myotonica, WD repeat containing
Synonyms D19S593E; DMR-N9; DMRN9; gene59
Species Homo sapiens
Ensembl Gene ENSG00000185800
Encoded Proteins
dystrophia myotonica, WD repeat containing
dystrophia myotonica, WD repeat containing
dystrophia myotonica, WD repeat containing
dystrophia myotonica, WD repeat containing
dystrophia myotonica, WD repeat containing
dystrophia myotonica, WD repeat containing
dystrophia myotonica, WD repeat containing
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 19:45782947-45792802
Strand Reverse strand
Band q13.32
Transcripts
ENST00000270223 ENSP00000270223
ENST00000377735 ENSP00000366964
ENST00000537879 ENSP00000444820
ENST00000597053 ENSP00000473426
ENST00000598237 ENSP00000473415
ENST00000601370
ENST00000602829 ENSP00000473377
ENST00000602469
ENST00000615410 ENSP00000479715
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
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL G5E9A7 Q8WUW6
UniProt Splice Variant
Entrez Gene 1762
UniGene Hs.515474
RefSeq NM_004943
HUGO HGNC:2936
OMIM 609857
CCDS CCDS33054
HPRD
IMGT
EMBL AC011530 BC019266 BT006798 CH471126
GenPept AAH19266 AAP35444 EAW57386
RNA Seq Atlas 1762