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proteins. Page last changed on 19 Dec 2016.
Diffuse panbronchiolitis critical region 1
C6orf37, DPCR1, FAM46A
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Top mentioned proteins:
AGE, CAN, ACID, OUT, bcl-2
Papers on
C6orf37
Susceptibility to large-joint osteoarthritis (hip and knee) is associated with BAG6 rs3117582 SNP and the VNTR polymorphism in the second exon of the FAM46A gene on chromosome 6.
Oslo, Norway. In J Orthop Res, 2015
Family with sequence similarity 46, member A (FAM46A) gene VNTR and BCL2-Associated Athanogene 6 (BAG6) gene rs3117582 polymorphisms were genotyped in a case-control study with 474 large-joint (hip and knee) osteoarthritis (OA) patients and 568 controls in Croatian population by candidate-gene approach for association with OA.
Association of the FAM46A gene VNTRs and BAG6 rs3117582 SNP with non small cell lung cancer (NSCLC) in Croatian and Norwegian populations.
Oslo, Norway. In Plos One, 2014
We analyzed for associations between a variable number of tandem repeat (VNTR) polymorphism in the Family with sequence similarity 46, member A (FAM46A) gene and a single nucleotide polymorphism (rs3117582) in the BCL2-Associated Athanogene 6 (BAG6) with non small cell lung cancer in Croatian and Norwegian subjects.
Lower PRDM2 expression is associated with dopamine-agonist resistance and tumor recurrence in prolactinomas.
Beijing, China. In Bmc Cancer, 2014
New resistant variants were identified in multiple genes including PRDM2, PRG4, MUC4, DSPP, DPCR1, RP1L1, MX2, POTEF, C1orf170, and KRTAP10-3.
Long non-coding RNA deregulation in tongue squamous cell carcinoma.
Hong Kong, Hong Kong. In Biomed Res Int, 2013
Lnc-PPP2R4-5, lnc-SPRR2D-1, lnc-MAN1A2-1, lnc-FAM46A-1, lnc-MBL2-4:1, and lnc-MBL2-4:3 were upregulated in the microdissected tongue SCC tissues.
Variations in the MHC region confer risk to esophageal squamous cell carcinoma on the subjects from high-incidence area in northern China.
Zhengzhou, China. In Plos One, 2013
These three SNPs were located at the genes of HLA-DQA1, TRIM27, and DPCR1, respectively.
Association of variable number of tandem repeats in the coding region of the FAM46A gene, FAM46A rs11040 SNP and BAG6 rs3117582 SNP with susceptibility to tuberculosis.
Oslo, Norway. In Plos One, 2013
We analyzed for association between the Family with sequence similarity 46, member A (FAM46A) gene (located on chromosome 6q14.1),
Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders.
Jerusalem, Israel. In Front Neurosci, 2013
The most widely shared subset of genes-common to five of six disorders-included ANK3, AS3MT, CACNA1C, CACNB2, CNNM2, CSMD1, DPCR1, ITIH3, NT5C2, PPP1R11, SYNE1, TCF4, TENM4, TRIM26, and ZNRD1.
Blood transcriptomic biomarkers in adult primary care patients with major depressive disorder undergoing cognitive behavioral therapy.
Chicago, United States. In Transl Psychiatry, 2013
Blood transcript levels of nine markers of ADCY3, DGKA, FAM46A, IGSF4A/CADM1, KIAA1539, MARCKS, PSME1, RAPH1 and TLR7, differed significantly between participants with MDD (N=32) and ND controls (N=32) at baseline (q< 0.05).
Evaluating genome-wide association study-identified breast cancer risk variants in African-American women.
Nashville, United States. In Plos One, 2012
Three additional SNPs, including rs1011970 (9p21/CDKN2A/2B), rs941764 (14q32/CCDC88C), and rs17529111 (6q14/FAM46A), showed a significant association in analyses conducted by breast cancer subtype.
Effect of diffuse panbronchiolitis critical region 1 polymorphisms on the risk of aspirin-exacerbated respiratory disease in Korean asthmatics.
GeneRIF
Seoul, South Korea. In Respir Care, 2012
results show that polymorphisms in DPCR1 are not associated with the risk of aspirin-exacerbated respiratory disease in Korean asthmatics
Molecular cloning of two novel mucin-like genes in the disease-susceptibility locus for diffuse panbronchiolitis.
Tokyo, Japan. In Hum Genet, 2011
We cloned two novel mucin-like genes designated panbronchiolitis related mucin-like 1 and 2 (PBMUCL1 and PBMUCL2) in the candidate region, which form a mucin-like gene cluster together with two adjacent genes, MUC21 and DPCR1.
Gene expression profiling of metaplastic lineages identifies CDH17 as a prognostic marker in early stage gastric cancer.
Nashville, United States. In Gastroenterology, 2010
Immunostaining was detected for 12 proteins, including 3 new markers of IM (ACE2, LGALS4, AKR1B10) and 3 of SPEM (OLFM4, LYZ, DPCR1).
Gene expression profiles for predicting the efficacy of the anticancer drug 5-fluorouracil in breast cancer.
Kao-hsiung, Taiwan. In Dna Cell Biol, 2010
The experimental results demonstrated that FAM46A, IL18, CCL28, TNF, CXCL2, PLEKHA8, HRAS, FDXR, and CHI3L1 genes showed statistically significant differential expression between primary breast cancer culture cells that respond and nonrespond to 5-FU.
Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs.
GeneRIF
Sevilla, Spain. In Ann Hum Genet, 2008
Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterization of novel VNTRs is reported.
Identification of a novel VNTR polymorphism in C6orf37 and its association with colorectal cancer risk in Chinese population.
GeneRIF
Hangzhou, China. In Clin Chim Acta, 2006
A novel VNTR polymorphism in C6orf37 exists in Chinese population and is not associated with colorectal cancer risk
[Bioinformatic analysis of adenoma-normal mucosa SSH library of colon].
Hangzhou, China. In Yi Chuan, 2006
We also detected the expression of 2 genes with highest hits, Reg4 and FAM46A, by semi-quantitative RT-PCR.
Identification of novel candidate genes in the diffuse panbronchiolitis critical region of the class I human MHC.
GeneRIF
Isehara, Japan. In Immunogenetics, 2002
C6orf37OS (C6orf37 Opposite Strand). Unexpectedly, RT-PCR analysis detected transcripts from the anti-sense DNA strand of this C6orf37 locus in numerous tissues, with most-abundant expression in lung, kidney, and testis.
Identification and characterization of C6orf37, a novel candidate human retinal disease gene on chromosome 6q14.
GeneRIF
Edmonton, Canada. In Biochem Biophys Res Commun, 2002
a candidate of human retinal disease on chromosome 6
