DMWD (gene): Difference between revisions

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Latest revision as of 18:33, 30 August 2017

Dystrophia myotonica WD repeat-containing protein is a protein that in humans is encoded by the DMWD gene.^[1]^[2]

References

↑ 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.
↑ "Entrez Gene: DMWD dystrophia myotonica, WD repeat containing".

Groenen P, Wieringa B (1999). "Expanding complexity in myotonic dystrophy". BioEssays. 20 (11): 901–12. doi:10.1002/(SICI)1521-1878(199811)20:11<901::AID-BIES5>3.0.CO;2-0. PMID 9872056.
Wansink DG, Wieringa B (2004). "Transgenic mouse models for myotonic dystrophy type 1 (DM1)". Cytogenet. Genome Res. 100 (1–4): 230–42. doi:10.1159/000072859. PMID 14526185.
Jansen G, Bächner D, Coerwinkel M, et al. (1995). "Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus". Hum. Mol. Genet. 4 (5): 843–52. doi:10.1093/hmg/4.5.843. PMID 7633444.
Shaw DJ, McCurrach M, Rundle SA, et al. (1994). "Genomic organization and transcriptional units at the myotonic dystrophy locus". Genomics. 18 (3): 673–9. doi:10.1016/S0888-7543(05)80372-6. PMID 7905855.
Mahadevan MS, Amemiya C, Jansen G, et al. (1993). "Structure and genomic sequence of the myotonic dystrophy (DM kinase) gene". Hum. Mol. Genet. 2 (3): 299–304. doi:10.1093/hmg/2.3.299. PMID 8499920.
Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
Alwazzan M, Newman E, Hamshere MG, Brook JD (1999). "Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat". Hum. Mol. Genet. 8 (8): 1491–7. doi:10.1093/hmg/8.8.1491. PMID 10400997.
Eriksson M, Hedberg B, Carey N, Ansved T (2001). "Decreased DMPK transcript levels in myotonic dystrophy 1 type IIA muscle fibers". Biochem. Biophys. Res. Commun. 286 (5): 1177–82. doi:10.1006/bbrc.2001.5516. PMID 11527424.
Frisch R, Singleton KR, Moses PA, et al. (2001). "Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy". Mol. Genet. Metab. 74 (1–2): 281–91. doi:10.1006/mgme.2001.3229. PMID 11592825.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Grimwood J, Gordon LA, Olsen A, et al. (2004). "The DNA sequence and biology of human chromosome 19". Nature. 428 (6982): 529–35. doi:10.1038/nature02399. PMID 15057824.
Beausoleil SA, Jedrychowski M, Schwartz D, et al. (2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins". Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130–5. doi:10.1073/pnas.0404720101. PMC 514446. PMID 15302935.

This article on a gene on human chromosome 19 is a stub. You can help Wikipedia by expanding it.

[pmid1302022-1] 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.

[entrez-2] "Entrez Gene: DMWD dystrophia myotonica, WD repeat containing".

[1]

[2]

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+'''Dystrophia myotonica WD repeat-containing protein''' is a [[protein]] that in humans is encoded by the ''DMWD'' [[gene]].<ref name="pmid1302022">{{cite journal | vauthors = Jansen G, Mahadevan M, Amemiya C, Wormskamp N, Segers B, Hendriks W, O'Hoy K, Baird S, Sabourin L, Lennon G | title = Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs | journal = Nat Genet | volume = 1 | issue = 4 | pages = 261–6 |date=Jun 1993 | pmid = 1302022 | pmc =  | doi = 10.1038/ng0792-261 |display-authors=etal}}</ref><ref name="entrez">{{cite web | title = Entrez Gene: DMWD dystrophia myotonica, WD repeat containing| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1762| accessdate = }}</ref>
- | image =
- | image_source =
- | PDB =
- | Name = Dystrophia myotonica, WD repeat containing
- | HGNCid = 2936
- | Symbol = DMWD
- | AltSymbols =; D19S593E; DMR-N9; DMRN9; gene59
- | OMIM = 609857
- | ECnumber =
- | Homologene = 22559
- | MGIid = 94907
- | GeneAtlas_image1 = PBB_GE_DMWD_213231_at_tn.png
- | GeneAtlas_image2 = PBB_GE_DMWD_33768_at_tn.png
- | Function = {{GNF_GO|id=GO:0003674 |text = molecular_function}}
- | Component = {{GNF_GO|id=GO:0005575 |text = cellular_component}}
- | Process = {{GNF_GO|id=GO:0007126 |text = meiosis}}
- | Orthologs = {{GNF_Ortholog_box
-    | Hs_EntrezGene = 1762
-    | Hs_Ensembl = ENSG00000185800
-    | Hs_RefseqProtein = NP_004934
-    | Hs_RefseqmRNA = NM_004943
-    | Hs_GenLoc_db =
-    | Hs_GenLoc_chr = 19
-    | Hs_GenLoc_start = 50979324
-    | Hs_GenLoc_end = 50987866
-    | Hs_Uniprot = Q09019
-    | Mm_EntrezGene = 13401
-    | Mm_Ensembl = ENSMUSG00000030410
-    | Mm_RefseqmRNA = XM_986190
-    | Mm_RefseqProtein = XP_991284
-    | Mm_GenLoc_db =
-    | Mm_GenLoc_chr = 7
-    | Mm_GenLoc_start = 18234837
-    | Mm_GenLoc_end = 18241297
-    | Mm_Uniprot = Q8K0I9
-  }}
-}}
-'''Dystrophia myotonica, WD repeat containing''', also known as '''DMWD''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: DMWD dystrophia myotonica, WD repeat containing| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1762| accessdate = }}</ref>
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@@ Line 56: / Line 11: @@
 ==References==
-{{reflist|2}}
+{{reflist}}
 ==Further reading==
 {{refbegin | 2}}
 {{PBB_Further_reading
 | citations =
-*{{cite journal  | author=Groenen P, Wieringa B |title=Expanding complexity in myotonic dystrophy. |journal=Bioessays |volume=20 |issue= 11 |pages= 901-12 |year= 1999 |pmid= 9872056 |doi= 10.1002/(SICI)1521-1878(199811)20:11<901::AID-BIES5>3.0.CO;2-0 }}
+*{{cite journal  | vauthors=Groenen P, Wieringa B |title=Expanding complexity in myotonic dystrophy. |journal=BioEssays |volume=20 |issue= 11 |pages= 901–12 |year= 1999 |pmid= 9872056 |doi= 10.1002/(SICI)1521-1878(199811)20:11<901::AID-BIES5>3.0.CO;2-0 }}
-*{{cite journal  | author=Wansink DG, Wieringa B |title=Transgenic mouse models for myotonic dystrophy type 1 (DM1). |journal=Cytogenet. Genome Res. |volume=100 |issue= 1-4 |pages= 230-42 |year= 2004 |pmid= 14526185 |doi= 10.1159/000072859 }}
+*{{cite journal  | vauthors=Wansink DG, Wieringa B |title=Transgenic mouse models for myotonic dystrophy type 1 (DM1). |journal=Cytogenet. Genome Res. |volume=100 |issue= 1–4 |pages= 230–42 |year= 2004 |pmid= 14526185 |doi= 10.1159/000072859 }}
-*{{cite journal  | author=Jansen G, Mahadevan M, Amemiya C, ''et al.'' |title=Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs. |journal=Nat. Genet. |volume=1 |issue= 4 |pages= 261-6 |year= 1993 |pmid= 1302022 |doi= 10.1038/ng0792-261 }}
+*{{cite journal  | vauthors=Jansen G, Bächner D, Coerwinkel M |title=Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus |journal=Hum. Mol. Genet. |volume=4 |issue= 5 |pages= 843–52 |year= 1995 |pmid= 7633444 |doi=10.1093/hmg/4.5.843  |display-authors=etal}}
-*{{cite journal  | author=Jansen G, Bächner D, Coerwinkel M, ''et al.'' |title=Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus. |journal=Hum. Mol. Genet. |volume=4 |issue= 5 |pages= 843-52 |year= 1995 |pmid= 7633444 |doi=  }}
+*{{cite journal  | vauthors=Shaw DJ, McCurrach M, Rundle SA |title=Genomic organization and transcriptional units at the myotonic dystrophy locus |journal=Genomics |volume=18 |issue= 3 |pages= 673–9 |year= 1994 |pmid= 7905855 |doi=10.1016/S0888-7543(05)80372-6  |display-authors=etal}}
-*{{cite journal  | author=Shaw DJ, McCurrach M, Rundle SA, ''et al.'' |title=Genomic organization and transcriptional units at the myotonic dystrophy locus. |journal=Genomics |volume=18 |issue= 3 |pages= 673-9 |year= 1994 |pmid= 7905855 |doi=  }}
+*{{cite journal  | vauthors=Mahadevan MS, Amemiya C, Jansen G |title=Structure and genomic sequence of the myotonic dystrophy (DM kinase) gene |journal=Hum. Mol. Genet. |volume=2 |issue= 3 |pages= 299–304 |year= 1993 |pmid= 8499920 |doi=10.1093/hmg/2.3.299  |display-authors=etal}}
-*{{cite journal  | author=Mahadevan MS, Amemiya C, Jansen G, ''et al.'' |title=Structure and genomic sequence of the myotonic dystrophy (DM kinase) gene. |journal=Hum. Mol. Genet. |volume=2 |issue= 3 |pages= 299-304 |year= 1993 |pmid= 8499920 |doi=  }}
+*{{cite journal  | vauthors=Bonaldo MF, Lennon G, Soares MB |title=Normalization and subtraction: two approaches to facilitate gene discovery |journal=Genome Res. |volume=6 |issue= 9 |pages= 791–806 |year= 1997 |pmid= 8889548 |doi=10.1101/gr.6.9.791  }}
-*{{cite journal  | author=Bonaldo MF, Lennon G, Soares MB |title=Normalization and subtraction: two approaches to facilitate gene discovery. |journal=Genome Res. |volume=6 |issue= 9 |pages= 791-806 |year= 1997 |pmid= 8889548 |doi=  }}
+*{{cite journal  | vauthors=Alwazzan M, Newman E, Hamshere MG, Brook JD |title=Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat |journal=Hum. Mol. Genet. |volume=8 |issue= 8 |pages= 1491–7 |year= 1999 |pmid= 10400997 |doi=10.1093/hmg/8.8.1491  }}
-*{{cite journal  | author=Alwazzan M, Newman E, Hamshere MG, Brook JD |title=Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat. |journal=Hum. Mol. Genet. |volume=8 |issue= 8 |pages= 1491-7 |year= 1999 |pmid= 10400997 |doi=  }}
+*{{cite journal  | vauthors=Eriksson M, Hedberg B, Carey N, Ansved T |title=Decreased DMPK transcript levels in myotonic dystrophy 1 type IIA muscle fibers |journal=Biochem. Biophys. Res. Commun. |volume=286 |issue= 5 |pages= 1177–82 |year= 2001 |pmid= 11527424 |doi= 10.1006/bbrc.2001.5516 }}
-*{{cite journal  | author=Eriksson M, Hedberg B, Carey N, Ansved T |title=Decreased DMPK transcript levels in myotonic dystrophy 1 type IIA muscle fibers. |journal=Biochem. Biophys. Res. Commun. |volume=286 |issue= 5 |pages= 1177-82 |year= 2001 |pmid= 11527424 |doi= 10.1006/bbrc.2001.5516 }}
+*{{cite journal  | vauthors=Frisch R, Singleton KR, Moses PA |title=Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy |journal=Mol. Genet. Metab. |volume=74 |issue= 1–2 |pages= 281–91 |year= 2001 |pmid= 11592825 |doi= 10.1006/mgme.2001.3229 |display-authors=etal}}
-*{{cite journal  | author=Frisch R, Singleton KR, Moses PA, ''et al.'' |title=Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy. |journal=Mol. Genet. Metab. |volume=74 |issue= 1-2 |pages= 281-91 |year= 2001 |pmid= 11592825 |doi= 10.1006/mgme.2001.3229 }}
+*{{cite journal  | vauthors=Strausberg RL, Feingold EA, Grouse LH |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 |display-authors=etal}}
-*{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
+*{{cite journal  | vauthors=Grimwood J, Gordon LA, Olsen A |title=The DNA sequence and biology of human chromosome 19 |journal=Nature |volume=428 |issue= 6982 |pages= 529–35 |year= 2004 |pmid= 15057824 |doi= 10.1038/nature02399 |display-authors=etal}}
-*{{cite journal  | author=Grimwood J, Gordon LA, Olsen A, ''et al.'' |title=The DNA sequence and biology of human chromosome 19. |journal=Nature |volume=428 |issue= 6982 |pages= 529-35 |year= 2004 |pmid= 15057824 |doi= 10.1038/nature02399 }}
+*{{cite journal  | vauthors=Beausoleil SA, Jedrychowski M, Schwartz D |title=Large-scale characterization of HeLa cell nuclear phosphoproteins |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 33 |pages= 12130–5 |year= 2004 |pmid= 15302935 |doi= 10.1073/pnas.0404720101  | pmc=514446 |display-authors=etal}}
-*{{cite journal  | author=Beausoleil SA, Jedrychowski M, Schwartz D, ''et al.'' |title=Large-scale characterization of HeLa cell nuclear phosphoproteins. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 33 |pages= 12130-5 |year= 2004 |pmid= 15302935 |doi= 10.1073/pnas.0404720101 }}
 }}
 {{refend}}
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DMWD (gene): Difference between revisions

Latest revision as of 18:33, 30 August 2017

References

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