CDC123

General Information

Full gene name:cell division cycle 123 homolog (S. cerevisiae)
Entrez Gene ID:8872
Location:10p13
Synonyms:D123, C10orf7
Type:protein-coding

User SNPs

SNPs given by the user that are near or inside this gene:

SNP Distance (bp) Direction
rs12779790 35421 downstream

NCBI Summary

None available.

OMIM

No OMIM data available for this gene.

NCBI Phenotypes

  • Identification of new genetic risk variants for type 2 diabetes.
  • NHGRI GWA Catalog
  • Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
  • Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.

Gene Ontology

  • G1 phase of mitotic cell cycle
  • cell cycle arrest
  • cell division
  • cytoplasm
  • regulation of mitotic cell cycle
  • positive regulation of cell proliferation

KEGG Pathways

No pathways found linked to this gene.

GeneRIFs

  • Observational study of gene-disease association, gene-gene interaction, and gene-environment interaction. (HuGE Navigator) [PMID 20889853]
  • Affinity Capture-MS [PMID 21987572]
  • Observational study of gene-disease association. (HuGE Navigator) [PMID 20816152]
  • Observational study and meta-analysis of gene-disease association. (HuGE Navigator) [PMID 20927120]
  • Observational study of gene-disease association, gene-gene interaction, gene-environment interaction, and genetic testing. (HuGE Navigator) [PMID 20075150]
  • Meta-analysis and genome-wide association study of gene-disease association. (HuGE Navigator) [PMID 18372903]
  • Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) [PMID 20379614]
  • A significant association of rs10906115 in CDC123/CAMK1D and rs1359790 near SPRY2 was identified with type 2 diabetes in a Japanese population. [PMID 21909839]
  • Dosage Rescue [PMID 15319434]
  • Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) [PMID 20571754]
  • Meta-analysis and HuGE review of gene-disease association. (HuGE Navigator) [PMID 19602701]
  • Observational study of gene-disease association, gene-gene interaction, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) [PMID 20879858]

PubMed Articles

Recent articles:

  • Lee KA et al. “Ubiquitin ligase substrate identification through quantitative proteomics at both the protein and peptide levels.” J Biol Chem. 2011 Dec 2;286(48):41530-8. PMID 21987572
  • Imamura M et al. “Genetic variants at CDC123/CAMK1D and SPRY2 are associated with susceptibility to type 2 diabetes in the Japanese population.” Diabetologia. 2011 Dec;54(12):3071-7. PMID 21909839
  • Kim W et al. “Systematic and quantitative assessment of the ubiquitin-modified proteome.” Mol Cell. 2011 Oct 21;44(2):325-40. PMID 21906983
  • Wagner SA et al. “A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles.” Mol Cell Proteomics. 2011 Oct;10(10):M111.013284. PMID 21890473
  • Soler Artigas M et al. “Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.” Nat Genet. 2011 Sep 25;43(11):1082-90. PMID 21946350
  • Danielsen JM et al. “Mass spectrometric analysis of lysine ubiquitylation reveals promiscuity at site level.” Mol Cell Proteomics. 2011 Mar;10(3):M110.003590. PMID 21139048
  • de Miguel-Yanes JM et al. “Genetic risk reclassification for type 2 diabetes by age below or above 50 years using 40 type 2 diabetes risk single nucleotide polymorphisms.” Diabetes Care. 2011 Jan;34(1):121-5. PMID 20889853
  • Zhou DZ et al. “Variations in/nearby genes coding for JAZF1, TSPAN8/LGR5 and HHEX-IDE and risk of type 2 diabetes in Han Chinese.” J Hum Genet. 2010 Dec;55(12):810-5. PMID 20927120
  • Rotger M et al. “Impact of single nucleotide polymorphisms and of clinical risk factors on new‐onset diabetes mellitus in HIV‐infected individuals.” Clin Infect Dis. 2010 Nov 1;51(9):1090-8. PMID 20879858
  • Shu XO et al. “Identification of new genetic risk variants for type 2 diabetes.” PLoS Genet. 2010 Sep 16;6(9). PMID 20862305

Top Pubmed articles linked to gene CDC123 matching any search term:

  • Imamura M et al. “Genetic variants at CDC123/CAMK1D and SPRY2 are associated with susceptibility to type 2 diabetes in the Japanese population.” Diabetologia. 2011 Dec;54(12):3071-7. PMID 21909839
  • Vangipurapu J et al. “Association of indices of liver and adipocyte insulin resistance with 19 confirmed susceptibility loci for type 2 diabetes in 6,733 non-diabetic Finnish men.” Diabetologia. 2011 Mar;54(3):563-71. PMID 21153532
  • de Miguel-Yanes JM et al. “Genetic risk reclassification for type 2 diabetes by age below or above 50 years using 40 type 2 diabetes risk single nucleotide polymorphisms.” Diabetes Care. 2011 Jan;34(1):121-5. PMID 20889853
  • Zhou DZ et al. “Variations in/nearby genes coding for JAZF1, TSPAN8/LGR5 and HHEX-IDE and risk of type 2 diabetes in Han Chinese.” J Hum Genet. 2010 Dec;55(12):810-5. PMID 20927120
  • Stuebe AM et al. “Obesity and diabetes genetic variants associated with gestational weight gain.” Am J Obstet Gynecol. 2010 Sep;203(3):283.e1-17. PMID 20816152
  • Morgan AR et al. “Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study.” BMC Med Genet. 2010 Aug 16;11:125. PMID 20712903
  • Zhao J et al. “Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.” Diabetes. 2010 Mar;59(3):751-5. PMID 19933996
  • Wen J et al. “Investigation of type 2 diabetes risk alleles support CDKN2A/B, CDKAL1, and TCF7L2 as susceptibility genes in a Han Chinese cohort.” PLoS One. 2010 Feb 10;5(2):e9153. PMID 20161779
  • Talmud PJ et al. “Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort study.” BMJ. 2010 Jan 14;340:b4838. PMID 20075150
  • Schleinitz D et al. “Lack of significant effects of the type 2 diabetes susceptibility loci JAZF1, CDC123/CAMK1D, NOTCH2, ADAMTS9, THADA, and TSPAN8/LGR5 on diabetes and quantitative metabolic traits.” Horm Metab Res. 2010 Jan;42(1):14-22. PMID 19670153
  • Simonis-Bik AM et al. “Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function.” Diabetes. 2010 Jan;59(1):293-301. PMID 19833888
  • Lango Allen H et al. “Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes.” Diabetes. 2010 Jan;59(1):266-71. PMID 19794065
  • Boesgaard TW et al. “Variant near ADAMTS9 known to associate with type 2 diabetes is related to insulin resistance in offspring of type 2 diabetes patients–EUGENE2 study.” PLoS One. 2009 Sep 30;4(9):e7236. PMID 19789630
  • Kang ES et al. “Association of common type 2 diabetes risk gene variants and posttransplantation diabetes mellitus in renal allograft recipients in Korea.” Transplantation. 2009 Sep 15;88(5):693-8. PMID 19741467
  • Stancáková A et al. “Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men.” Diabetes. 2009 Sep;58(9):2129-36. PMID 19502414
  • Omori S et al. “Replication study for the association of new meta-analysis-derived risk loci with susceptibility to type 2 diabetes in 6,244 Japanese individuals.” Diabetologia. 2009 Aug;52(8):1554-60. PMID 19455301

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