Biology:CC2D1A
From HandWiki
Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
Coiled-coil and C2 domain-containing protein 1A is a protein that in humans is encoded by the CC2D1A gene.[1][2][3]
References
- ↑ "Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways". Oncogene 22 (21): 3307–18. May 2003. doi:10.1038/sj.onc.1206406. PMID 12761501.
- ↑ "The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non‐syndromic mental retardation". J Med Genet 43 (3): 203–10. Mar 2006. doi:10.1136/jmg.2005.035709. PMID 16033914.
- ↑ "Entrez Gene: CC2D1A coiled-coil and C2 domain containing 1A". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=54862.
External links
- Human CC2D1A genome location and CC2D1A gene details page in the UCSC Genome Browser.
Further reading
- "5-HT1A receptors, gene repression, and depression: guilt by association". The Neuroscientist 10 (6): 575–93. 2005. doi:10.1177/1073858404267382. PMID 15534042.
- 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. PMID 12477932. Bibcode: 2002PNAS...9916899M.
- Basel-Vanagaite L; Alkelai A; Straussberg R et al. (2003). "Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity". J. Med. Genet. 40 (10): 729–32. doi:10.1136/jmg.40.10.729. PMID 14569116.
- Ota T; Suzuki Y; Nishikawa T et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- "Cell type-dependent recruitment of trichostatin A-sensitive repression of the human 5-HT1A receptor gene". J. Neurochem. 88 (4): 857–68. 2004. doi:10.1046/j.1471-4159.2003.02223.x. PMID 14756806.
- Gerhard DS; Wagner L; Feingold EA et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.
- Rush J; Moritz A; Lee KA et al. (2005). "Immunoaffinity profiling of tyrosine phosphorylation in cancer cells". Nat. Biotechnol. 23 (1): 94–101. doi:10.1038/nbt1046. PMID 15592455.
- Beausoleil SA; Villén J; Gerber SA et al. (2006). "A probability-based approach for high-throughput protein phosphorylation analysis and site localization". Nat. Biotechnol. 24 (10): 1285–92. doi:10.1038/nbt1240. PMID 16964243.
- Rogaeva A; Ou XM; Jafar-Nejad H et al. (2007). "Differential repression by freud-1/CC2D1A at a polymorphic site in the dopamine-D2 receptor gene". J. Biol. Chem. 282 (29): 20897–905. doi:10.1074/jbc.M610038200. PMID 17535813.
- "The mental retardation gene CC2D1A/Freud-1 encodes a long isoform that binds conserved DNA elements to repress gene transcription". Eur. J. Neurosci. 26 (4): 965–74. 2007. doi:10.1111/j.1460-9568.2007.05727.x. PMID 17714190.
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