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DMWD (gene)

From Wikipedia, the free encyclopedia
DMWD
Identifiers
AliasesDMWD, D19S593E, DMR-N9, DMRN9, gene59, dystrophia myotonica, WD repeat containing, DM1 locus, WD repeat containing
External IDsOMIM: 609857; MGI: 94907; HomoloGene: 22559; GeneCards: DMWD; OMA:DMWD - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004943

NM_010058
NM_001374607

RefSeq (protein)

NP_004934

NP_034188
NP_001361536

Location (UCSC)Chr 19: 45.78 – 45.79 MbChr 7: 18.81 – 18.82 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Dystrophia myotonica WD repeat-containing protein is a protein that in humans is encoded by the DMWD gene.[5][6]


References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000185800Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030410Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Jansen G, Mahadevan M, Amemiya C, Wormskamp N, Segers B, Hendriks W, O'Hoy K, Baird S, Sabourin L, Lennon G, et al. (Jun 1993). "Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs". Nat Genet. 1 (4): 261–6. doi:10.1038/ng0792-261. PMID 1302022. S2CID 26072532.
  6. ^ "Entrez Gene: DMWD dystrophia myotonica, WD repeat containing".

Further reading

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