Biology:ZBTB20
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Short description: Human protein-coding gene
 Generic protein structure example |
Zinc finger and BTB domain-containing protein 20 is a protein that in humans is encoded by the ZBTB20 gene.[1][2][3]
A mutation in a ZBTB20 gene causes Primrose syndrome.[4]
References
- ↑ "Assignment of the human zinc finger gene, ZNF288, to chromosome 3 band q13.2 by radiation hybrid mapping and fluorescence in situ hybridisation". Cytogenetics and Cell Genetics 89 (3–4): 156–157. Sep 2000. doi:10.1159/000015600. PMID 10965110.
- ↑ "Identification and characterization of DPZF, a novel human BTB/POZ zinc finger protein sharing homology to BCL-6". Biochemical and Biophysical Research Communications 282 (4): 1067–1073. April 2001. doi:10.1006/bbrc.2001.4689. PMID 11352661. Bibcode: 2001BBRC..282.1067Z.
- ↑ "Entrez Gene: ZBTB20 zinc finger and BTB domain containing 20". https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=26137.
- ↑ "Entry- #259050 - PRIMROSE SYNDROME; PRIMS- OMIM- (OMIM.ORG)" (in en-us). https://www.omim.org/entry/259050.
Further reading
- "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene 138 (1–2): 171–174. January 1994. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene 200 (1–2): 149–156. October 1997. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- "DNA cloning using in vitro site-specific recombination". Genome Research 10 (11): 1788–1795. November 2000. doi:10.1101/gr.143000. PMID 11076863.
- "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Research 11 (3): 422–435. March 2001. doi:10.1101/gr.GR1547R. PMID 11230166.
- "From ORFeome to biology: a functional genomics pipeline". Genome Research 14 (10B): 2136–2144. October 2004. doi:10.1101/gr.2576704. PMID 15489336.
- "The LIFEdb database in 2006". Nucleic Acids Research 34 (Database issue): D415–D418. January 2006. doi:10.1093/nar/gkj139. PMID 16381901.
- "Mutations in ZBTB20 cause Primrose syndrome". Nature Genetics 46 (8): 815–817. August 2014. doi:10.1038/ng.3035. PMID 25017102.
External links
- ZBTB20+protein,+human at the US 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.
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