
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
CORO1C
Introduction
Coronin-1C is a protein that in humans is encoded by the CORO1C gene.[1][2][3]
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation.[3]
References
References
- ↑ Okumura M, Kung C, Wong S, Rodgers M, Thomas ML (Oct 1998). “Definition of family of coronin-related proteins conserved between humans and mice: close genetic linkage between coronin-2 and CD45-associated protein”. DNA Cell Biol. 17 (9): 779–87. doi:10.1089/dna.1998.17.779. PMID 9778037.
- ↑ de Hostos EL (Oct 1999). “The coronin family of actin-associated proteins”. Trends Cell Biol. 9 (9): 345–50. doi:10.1016/S0962-8924(99)01620-7. PMID 10461187.
- ↑ 3.0 3.1 “Entrez Gene: CORO1C coronin, actin binding protein, 1C”.
External links
External links
- Human CORO1C genome location and CORO1C gene details page in the UCSC Genome Browser.
Further reading
Further reading
- Rosentreter A, Hofmann A, Xavier CP, et al. (2007). “Coronin 3 involvement in F-actin-dependent processes at the cell cortex”. Exp. Cell Res. 313 (5): 878–95. doi:10.1016/j.yexcr.2006.12.015. PMID 17274980.
- 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.
- 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. PMC 528928. PMID 15489334.
- 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.
- 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.
- Spoerl Z, Stumpf M, Noegel AA, Hasse A (2003). “Oligomerization, F-actin interaction, and membrane association of the ubiquitous mammalian coronin 3 are mediated by its carboxyl terminus”. J. Biol. Chem. 277 (50): 48858–67. doi:10.1074/jbc.M205136200. PMID 12377779.
- Iizaka M, Han HJ, Akashi H, et al. (2000). “Isolation and chromosomal assignment of a novel human gene, CORO1C, homologous to coronin-like actin-binding proteins”. Cytogenet. Cell Genet. 88 (3–4): 221–4. doi:10.1159/000015555. PMID 10828594.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). “Construction and characterization of a full length-enriched and a 5′-end-enriched cDNA library”. Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Wick M, Bürger C, Brüsselbach S, et al. (1994). “Identification of serum-inducible genes: different patterns of gene regulation during G0–>S and G1–>S progression”. J. Cell Sci. 107 (1): 227–39. PMID 8175911.
- Maruyama K, Sugano S (1994). “Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides”. Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
