Property Summary

NCBI Gene PubMed Count 30
PubMed Score 14.85
PubTator Score 9.42

Knowledge Summary


No data available


  Differential Expression (5)

Disease log2 FC p
osteosarcoma -1.590 1.5e-06
group 3 medulloblastoma 2.300 3.8e-03
atypical teratoid / rhabdoid tumor -1.200 1.3e-04
tuberculosis 1.700 4.0e-07
ovarian cancer 1.200 3.7e-05

Protein-protein Interaction (6)

Gene RIF (12)

24157943 Variants in NPHS2, SDCCAG8 and near BMP4 appear to interact with APOL1 to modulate the risk for non-diabetic end stage kidney disease in african americans.
22626039 Our results and prior literature suggest that SDCCAG8 could play an important role in presumed Bardet-Biedl syndrome (BBS) patients affected with severe kidney disease and absent polydactyly.
22614287 significant associations in schizophrenia to SDCAAG8 and extensive replication of associations reported by the Schizophrenia.
22190034 HIV-1 MA is identified to have a physical interaction with serologically defined colon cancer antigen 8 (SDCCAG8) in human HEK293 and/or Jurkat cell lines by using affinity tagging and purification mass spectrometry analyses
22095114 Intronic variants of SDCCAG8, which are associated with early onset obesity, are associated with reduced weight loss after a 1-year lifestyle intervention in overweight children and adolescents even after adjusting for age, sex, baseline measurement.
20835237 Mutation of SDCCAG8 is associated with retinal-renal ciliopathy.
20628086 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
20421936 Meta-analysis and genome-wide association study of gene-disease association. (HuGE Navigator)
20379614 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
20056178 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
19913121 Observational study of gene-disease association. (HuGE Navigator)
19626040 Observational study of gene-disease association. (HuGE Navigator)

AA Sequence

LRTQLPSMPQSDC                                                             701 - 713

Text Mined References (29)

PMID Year Title
25343990 2015 Genome-wide association study of selenium concentrations.
25201988 2014 Common genetic variants associated with cognitive performance identified using the proxy-phenotype method.
25056061 2014 Biological insights from 108 schizophrenia-associated genetic loci.
24166486 2013 GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus.
24157943 2014 Gene-gene interactions in APOL1-associated nephropathy.
23974872 2013 Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
23186163 2013 Toward a comprehensive characterization of a human cancer cell phosphoproteome.
22940612 2012 FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies.
22626039 2012 Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactyly.
22614287 2013 Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.
22190034 2011 Global landscape of HIV-human protein complexes.
22095114 2012 SDCCAG8 obesity alleles and reduced weight loss after a lifestyle intervention in overweight children and adolescents.
21926974 2011 Genome-wide association study identifies five new schizophrenia loci.
21399614 2011 Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods.
20835237 2010 Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy.
20628086 2010 Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
20421936 2010 Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.
20379614 Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
20056178 2010 Polymorphisms in innate immunity genes and patients response to dendritic cell-based HIV immuno-treatment.
19913121 2009 Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
19626040 2009 Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.
15489334 2004 The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
15146197 2004 Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation.
14702039 2004 Complete sequencing and characterization of 21,243 full-length human cDNAs.
14654843 2003 Proteomic characterization of the human centrosome by protein correlation profiling.
12559564 2003 Identification and characterization of the novel centrosome-associated protein CCCAP.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
11042152 2000 Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells.
9610721 1998 Characterization of human colon cancer antigens recognized by autologous antibodies.