CNBP: Difference between revisions

CNBP
Identifiers
Aliases	CNBP, CNBP1, DM2, PROMM, RNF163, ZCCHC22, ZNF9, CCHC-type zinc finger nucleic acid binding protein
External IDs	OMIM: 116955 MGI: 88431 HomoloGene: 2567 GeneCards: CNBP
Gene location (Human)
Chr.	Chromosome 3 (human)
End	129,183,922 bp
Gene location (Mouse)
Chr.	Chromosome 6 (mouse)
End	87,828,088 bp
RNA expression pattern
	Top expressed in
	thoracic diaphragm; ; biceps brachii; ; oocyte; ; Achilles tendon; ; gastrocnemius muscle; ; seminal vesicula; ; parotid gland; ; right ventricle; ; germinal epithelium; ; amniotic fluid;
	Top expressed in
	otic placode; ; saccule; ; primitive streak; ; abdominal wall; ; hair follicle; ; triceps brachii muscle; ; vastus lateralis muscle; ; intercostal muscle; ; dermis; ; seminal vesicula;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding; nucleic acid binding; zinc ion binding; DNA-binding transcription factor activity; metal ion binding; DNA binding; single-stranded DNA binding; single-stranded RNA binding; RNA binding; RNA polymerase II transcription regulatory region sequence-specific DNA binding; DNA-binding transcription repressor activity, RNA polymerase II-specific; mRNA binding; translation regulator activity;
Cellular component	nucleus; cytoplasm; endoplasmic reticulum; cytosol;
Biological process	regulation of transcription, DNA-templated; cholesterol biosynthetic process; transcription, DNA-templated; positive regulation of transcription by RNA polymerase II; positive regulation of transcription, DNA-templated; positive regulation of cell population proliferation; negative regulation of transcription by RNA polymerase II; positive regulation of cytoplasmic translation;
	Sources:Amigo / QuickGO
Orthologs
	7555
	12785
	ENSG00000169714
	ENSMUSG00000030057
	P62633
	P53996
NM_003418; NM_001127192; NM_001127193; NM_001127194; NM_001127195;
	NM_001127196
	NM_001109745; NM_001109746; NM_013493; NM_001347325; NM_001355195
NP_001120664; NP_001120665; NP_001120666; NP_001120667; NP_001120668;
	NP_003409
	NP_001103215; NP_001103216; NP_001334254; NP_038521; NP_001342124
	Wikidata
View/Edit Human	View/Edit Mouse

Browse history interactively

← Previous edit Next edit →

Content deleted Content added

VisualWikitext

Inline

Revision as of 10:30, 11 June 2008

Template:PBB Controls

CCHC-type zinc finger, nucleic acid binding protein, also known as CNBP, is a human gene.^[5]

Template:PBB Summary

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000169714 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000030057 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: CNBP CCHC-type zinc finger, nucleic acid binding protein".

External links

ZNF9+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

This article on a gene on human chromosome 3 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000169714 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000030057 – Ensembl, 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.

[entrez-5] "Entrez Gene: CNBP CCHC-type zinc finger, nucleic acid binding protein".

[1]

[2]

[3]

[4]

[5]

@@ Line 60: / Line 60: @@
 {{PBB_Further_reading
 | citations =
-*{{cite journal  | author=Lusis AJ, Rajavashisth TB, Klisak I, ''et al.'' |title=Mapping of the gene for CNBP, a finger protein, to human chromosome 3q13.3-q24. |journal=Genomics |volume=8 |issue= 2 |pages= 411-4 |year= 1991 |pmid= 2249857 |doi=  }}
+*{{cite journal  | author=Lusis AJ, Rajavashisth TB, Klisak I, ''et al.'' |title=Mapping of the gene for CNBP, a finger protein, to human chromosome 3q13.3-q24. |journal=Genomics |volume=8 |issue= 2 |pages= 411–4 |year= 1991 |pmid= 2249857 |doi=  }}
-*{{cite journal  | author=Rajavashisth TB, Taylor AK, Andalibi A, ''et al.'' |title=Identification of a zinc finger protein that binds to the sterol regulatory element. |journal=Science |volume=245 |issue= 4918 |pages= 640-3 |year= 1989 |pmid= 2562787 |doi=  }}
+*{{cite journal  | author=Rajavashisth TB, Taylor AK, Andalibi A, ''et al.'' |title=Identification of a zinc finger protein that binds to the sterol regulatory element. |journal=Science |volume=245 |issue= 4918 |pages= 640–3 |year= 1989 |pmid= 2562787 |doi=  }}
-*{{cite journal  | author=Flink IL, Morkin E |title=Organization of the gene encoding cellular nucleic acid-binding protein. |journal=Gene |volume=163 |issue= 2 |pages= 279-82 |year= 1995 |pmid= 7590281 |doi=  }}
+*{{cite journal  | author=Flink IL, Morkin E |title=Organization of the gene encoding cellular nucleic acid-binding protein. |journal=Gene |volume=163 |issue= 2 |pages= 279–82 |year= 1995 |pmid= 7590281 |doi=  }}
-*{{cite journal  | author=Warden CH, Krisans SK, Purcell-Huynh D, ''et al.'' |title=Mouse cellular nucleic acid binding proteins: a highly conserved family identified by genetic mapping and sequencing. |journal=Genomics |volume=24 |issue= 1 |pages= 14-9 |year= 1995 |pmid= 7896269 |doi= 10.1006/geno.1994.1576 }}
+*{{cite journal  | author=Warden CH, Krisans SK, Purcell-Huynh D, ''et al.'' |title=Mouse cellular nucleic acid binding proteins: a highly conserved family identified by genetic mapping and sequencing. |journal=Genomics |volume=24 |issue= 1 |pages= 14–9 |year= 1995 |pmid= 7896269 |doi= 10.1006/geno.1994.1576 }}
-*{{cite journal  | author=Ricker K, Grimm T, Koch MC, ''et al.'' |title=Linkage of proximal myotonic myopathy to chromosome 3q. |journal=Neurology |volume=52 |issue= 1 |pages= 170-1 |year= 1999 |pmid= 9921867 |doi=  }}
+*{{cite journal  | author=Ricker K, Grimm T, Koch MC, ''et al.'' |title=Linkage of proximal myotonic myopathy to chromosome 3q. |journal=Neurology |volume=52 |issue= 1 |pages= 170–1 |year= 1999 |pmid= 9921867 |doi=  }}
-*{{cite journal  | author=Liquori CL, Ricker K, Moseley ML, ''et al.'' |title=Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. |journal=Science |volume=293 |issue= 5531 |pages= 864-7 |year= 2001 |pmid= 11486088 |doi= 10.1126/science.1062125 }}
+*{{cite journal  | author=Liquori CL, Ricker K, Moseley ML, ''et al.'' |title=Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. |journal=Science |volume=293 |issue= 5531 |pages= 864–7 |year= 2001 |pmid= 11486088 |doi= 10.1126/science.1062125 }}
-*{{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  | 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  | author=McGrath CF, Buckman JS, Gagliardi TD, ''et al.'' |title=Human cellular nucleic acid-binding protein Zn2+ fingers support replication of human immunodeficiency virus type 1 when they are substituted in the nucleocapsid protein. |journal=J. Virol. |volume=77 |issue= 15 |pages= 8524-31 |year= 2003 |pmid= 12857921 |doi=  }}
+*{{cite journal  | author=McGrath CF, Buckman JS, Gagliardi TD, ''et al.'' |title=Human cellular nucleic acid-binding protein Zn2+ fingers support replication of human immunodeficiency virus type 1 when they are substituted in the nucleocapsid protein. |journal=J. Virol. |volume=77 |issue= 15 |pages= 8524–31 |year= 2003 |pmid= 12857921 |doi=  }}
-*{{cite journal  | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
+*{{cite journal  | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
-*{{cite journal  | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
+*{{cite journal  | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
-*{{cite journal  | author=Vallo L, Bonifazi E, Borgiani P, ''et al.'' |title=Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population. |journal=Mol. Cell. Probes |volume=19 |issue= 1 |pages= 71-4 |year= 2005 |pmid= 15652222 |doi= 10.1016/j.mcp.2004.09.003 }}
+*{{cite journal  | author=Vallo L, Bonifazi E, Borgiani P, ''et al.'' |title=Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population. |journal=Mol. Cell. Probes |volume=19 |issue= 1 |pages= 71–4 |year= 2005 |pmid= 15652222 |doi= 10.1016/j.mcp.2004.09.003 }}
-*{{cite journal  | author=Botta A, Caldarola S, Vallo L, ''et al.'' |title=Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2). |journal=Biochim. Biophys. Acta |volume=1762 |issue= 3 |pages= 329-34 |year= 2006 |pmid= 16376058 |doi= 10.1016/j.bbadis.2005.11.004 }}
+*{{cite journal  | author=Botta A, Caldarola S, Vallo L, ''et al.'' |title=Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2). |journal=Biochim. Biophys. Acta |volume=1762 |issue= 3 |pages= 329–34 |year= 2006 |pmid= 16376058 |doi= 10.1016/j.bbadis.2005.11.004 }}
-*{{cite journal  | author=Margolis JM, Schoser BG, Moseley ML, ''et al.'' |title=DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression. |journal=Hum. Mol. Genet. |volume=15 |issue= 11 |pages= 1808-15 |year= 2006 |pmid= 16624843 |doi= 10.1093/hmg/ddl103 }}
+*{{cite journal  | author=Margolis JM, Schoser BG, Moseley ML, ''et al.'' |title=DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression. |journal=Hum. Mol. Genet. |volume=15 |issue= 11 |pages= 1808–15 |year= 2006 |pmid= 16624843 |doi= 10.1093/hmg/ddl103 }}
-*{{cite journal  | author=Toth C, Dunham C, Suchowersky O, ''et al.'' |title=Unusual clinical, laboratory, and muscle histopathological findings in a family with myotonic dystrophy type 2. |journal=Muscle Nerve |volume=35 |issue= 2 |pages= 259-64 |year= 2007 |pmid= 17068784 |doi= 10.1002/mus.20685 }}
+*{{cite journal  | author=Toth C, Dunham C, Suchowersky O, ''et al.'' |title=Unusual clinical, laboratory, and muscle histopathological findings in a family with myotonic dystrophy type 2. |journal=Muscle Nerve |volume=35 |issue= 2 |pages= 259–64 |year= 2007 |pmid= 17068784 |doi= 10.1002/mus.20685 }}
-*{{cite journal  | author=Gerbasi VR, Link AJ |title=The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. |journal=Mol. Cell Proteomics |volume=6 |issue= 6 |pages= 1049-58 |year= 2007 |pmid= 17327219 |doi= 10.1074/mcp.M600384-MCP200 }}
+*{{cite journal  | author=Gerbasi VR, Link AJ |title=The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. |journal=Mol. Cell Proteomics |volume=6 |issue= 6 |pages= 1049–58 |year= 2007 |pmid= 17327219 |doi= 10.1074/mcp.M600384-MCP200 }}
 *{{cite journal  | author=Ewing RM, Chu P, Elisma F, ''et al.'' |title=Large-scale mapping of human protein-protein interactions by mass spectrometry. |journal=Mol. Syst. Biol. |volume=3 |issue=  |pages= 89 |year= 2007 |pmid= 17353931 |doi= 10.1038/msb4100134 }}
 }}

Revision as of 10:30, 11 June 2008

References

Further reading

External links