Open Access Articles- Top Results for ARVCF


SymbolsARVCF ; FLJ35345
External IDsOMIM602269 MGI109620 HomoloGene31046 GeneCards: ARVCF Gene
RNA expression pattern
File:PBB GE ARVCF 205784 x at tn.png
File:PBB GE ARVCF 217516 x at tn.png
More reference expression data
RefSeq (mRNA)NM_001670NM_001272028
RefSeq (protein)NP_001661NP_001258957
Location (UCSC)Chr 22:
19.96 – 20 Mb
Chr 16:
18.35 – 18.41 Mb
PubMed search[1][2]

Armadillo repeat protein deleted in velo-cardio-facial syndrome is a protein that in humans is encoded by the ARVCF gene.[1][2][3]


Armadillo repeat gene deleted in Velo-Cardio-Facial syndrome (ARVCF) is a member of the catenin family which play an important role in the formation of adherens junction complexes, which are thought to facilitate communication between the inside and outside environments of a cell. ARVCF gene was isolated in the search for the genetic defect responsible for the autosomal dominant Velo-Cardio-Facial syndrome (VCFS) a relatively common human disorder with phenotypic features including cleft palate, conotruncal heart defects and facial dysmorphology. ARVCF gene encodes a protein containing two motifs, a coiled coil domain in the N-terminus and a 10 armadillo repeat sequence in the midregion. Since these sequences can facilitate protein-protein interactions ARVCF is thought to function in a protein complex. In addition, ARVCF contains a predicted nuclear-targeting sequence suggesting that it may have a function as a nuclear protein.[3]


ARVCF has been shown to interact with CDH15.[4]


  1. ^ Sirotkin H, O'Donnell H, DasGupta R, Halford S, St Jore B, Puech A et al. (May 1997). "Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome". Genomics 41 (1): 75–83. PMID 9126485. doi:10.1006/geno.1997.4627. 
  2. ^ Kausalya PJ, Phua DC, Hunziker W (November 2004). "Association of ARVCF with Zonula Occludens (ZO)-1 and ZO-2: Binding to PDZ-Domain Proteins and Cell-Cell Adhesion Regulate Plasma Membrane and Nuclear Localization of ARVCF". Mol Biol Cell 15 (12): 5503–15. PMC 532029. PMID 15456900. doi:10.1091/mbc.E04-04-0350. 
  3. ^ a b "Entrez Gene: ARVCF armadillo repeat gene deletes in velocardiofacial syndrome". 
  4. ^ Kaufmann U, Zuppinger C, Waibler Z, Rudiger M, Urbich C, Martin B et al. (November 2000). "The armadillo repeat region targets ARVCF to cadherin-based cellular junctions". J. Cell. Sci. 113 (22): 4121–35. PMID 11058098. 

Further reading

  • Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS et al. (1995). "Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions". Am. J. Med. Genet. 57 (3): 514–22. PMID 7677167. doi:10.1002/ajmg.1320570339. 
  • Sirotkin H, Morrow B, Saint-Jore B, Puech A, Das Gupta R, Patanjali SR et al. (1997). "Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndrome". Genomics 42 (2): 245–51. PMID 9192844. doi:10.1006/geno.1997.4734. 
  • Bonné S, van Hengel J, van Roy F (1998). "Chromosomal mapping of human armadillo genes belonging to the p120(ctn)/plakophilin subfamily". Genomics 51 (3): 452–4. PMID 9721216. doi:10.1006/geno.1998.5398. 
  • Mariner DJ, Wang J, Reynolds AB (2000). "ARVCF localizes to the nucleus and adherens junction and is mutually exclusive with p120(ctn) in E-cadherin complexes". J. Cell. Sci. 113 (8): 1481–90. PMID 10725230. 
  • Kaufmann U, Zuppinger C, Waibler Z, Rudiger M, Urbich C, Martin B et al. (2001). "The armadillo repeat region targets ARVCF to cadherin-based cellular junctions". J. Cell. Sci. 113 (22): 4121–35. PMID 11058098. 
  • Laura RP, Witt AS, Held HA, Gerstner R, Deshayes K, Koehler MF et al. (2002). "The Erbin PDZ domain binds with high affinity and specificity to the carboxyl termini of delta-catenin and ARVCF". J. Biol. Chem. 277 (15): 12906–14. PMID 11821434. doi:10.1074/jbc.M200818200. 
  • Sanders AR, Rusu I, Duan J, Vander Molen JE, Hou C, Schwab SG et al. (2005). "Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia". Mol. Psychiatry 10 (4): 353–65. PMID 15340358. doi:10.1038/ 
  • Ballif BA, Villén J, Beausoleil SA, Schwartz D, Gygi SP (2005). "Phosphoproteomic analysis of the developing mouse brain". Mol. Cell Proteomics 3 (11): 1093–101. PMID 15345747. doi:10.1074/mcp.M400085-MCP200. 
  • Ulfig N, Chan WY (2005). "Expression of ARVCF in the human ganglionic eminence during fetal development". Dev. Neurosci. 26 (1): 38–44. PMID 15509897. doi:10.1159/000080710. 
  • Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C et al. (2006). "Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios". Am. J. Med. Genet. B Neuropsychiatr. Genet. 139 (1): 45–50. PMID 16118784. doi:10.1002/ajmg.b.30230. 

Lua error in package.lua at line 80: module 'Module:Buffer' not found.