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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

Zinc finger protein 365

UAN, Su48, ZNF365, ZNF365D
This gene encodes several isoforms which have different expression patterns and functions. Mutation in this gene is associated with uric acid nephrolithiasis (UAN). Alternatively spliced variants, encoding distinct proteins, have been identified. [provided by RefSeq, May 2010] (from NCBI)
Top mentioned proteins: AGE, HAD, ACID, CAN, TCPTP
Papers on UAN
Variants in 6q25.1 are associated with mammographic density in Malaysian Chinese women.
New
Teo et al., Malaysia. In Cancer Epidemiol Biomarkers Prev, Jan 2016
We could not replicate the most significant association found previously in European women (rs10995190, ZNF365 gene) because the minor allele was absent for Asian women.
Investigation of the association of Vogt-Koyanagi-Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai.
New
Yang et al., Chongqing, China. In Br J Ophthalmol, Jan 2016
The aim of the study was to replicate the association of IL23R-C1orf141 and ADO-ZNF365-EGR2 with VKH syndrome in four sets of multinational populations in Asia.
[Association between ZNF365 gene polymorphisms and bronchial asthma in children].
New
Cheng et al., Xianning, China. In Zhongguo Dang Dai Er Ke Za Zhi, Aug 2015
OBJECTIVE: To study the association of single nucleotide polymorphisms (SNP) (rs2393903 and rs10995251) in ZNF365 gene with bronchial asthma and its clinical characteristics in Han Chinese children in Hubei, China.
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression.
New
Chenevix-Trench et al., Stockholm, Sweden. In Am J Hum Genet, Aug 2015
Genome-wide association studies have identified SNPs near ZNF365 at 10q21.2 that are associated with both breast cancer risk and mammographic density.
Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures.
New
Vachon et al., Australia. In Cancer Res, Jul 2015
We found strong support for established associations between rs10995190 (in the region of ZNF365), rs2046210 (ESR1), and rs3817198 (LSP1) and adjusted absolute and percent dense areas (all P < 10(-5)).
Uric acid crystal could inhibit Numb-induced URAT1 lysosome degradation in uric acid nephropathy.
New
Zhou et al., Guangzhou, China. In J Physiol Biochem, Jun 2015
To investigate whether uric acid could regulate urate transporter 1 (URAT1) protein and activity level, we established uric acid nephropathy (UAN) rat model and detected their serum uric acid and URAT1 level with or without the treatment of allopurinol.
Pectoral muscle attenuation as a marker for breast cancer risk in full-field digital mammography.
New
Humphreys et al., Stockholm, Sweden. In Cancer Epidemiol Biomarkers Prev, Jun 2015
In addition, the controls dataset was used to test for the association of our measures against rs10995190, in the ZNF365 gene, a genetic variant known to be associated with mammography density and breast cancer risk.
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans.
Song et al., Seoul, South Korea. In Inflamm Bowel Dis, 2015
ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38),
Identification of two novel mammographic density loci at 6Q25.1.
Czene et al., Stockholm, Sweden. In Breast Cancer Res, 2014
RESULTS: Genome-wide significant associations were observed for two previously identified loci: ZNF365 (rs10995194, P = 2.3 × 10(-8) for percent MD and P = 8.7 × 10(-9) for absolute MD) and AREG (rs10034692, P = 6.7 × 10(-9) for absolute MD).
A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density.
Chang-Claude et al., Heidelberg, Germany. In Breast Cancer Res, 2014
We selected for evaluation 1327 single nucleotide polymorphisms (SNPs) showing the lowest P-values for interaction (P int) in a meta-analysis of genome-wide gene-environment interaction studies with MHT use on risk of breast cancer, 2541 SNPs in candidate genes (AKR1C4, CYP1A1-CYP1A2, CYP1B1, ESR2, PPARG, PRL, SULT1A1-SULT1A2 and TNF) and ten SNPs (AREG-rs10034692, PRDM6-rs186749, ESR1-rs12665607, ZNF365-rs10995190, 8p11.23-rs7816345,
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
Impact
Yang et al., Chongqing, China. In Nat Genet, 2014
ADO-ZNF365-EGR2, rs442309, P(combined) = 2.97 × 10(-11), OR = 1.37; and HLA-DRB1/DQA1, rs3021304, P(combined) = 1.26 × 10(-118), OR = 2.97).
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.
Impact
Tamari et al., Yokohama, Japan. In Nat Genet, 2012
On the basis of data from a genome-wide association study (GWAS) and a validation study comprising a total of 3,328 subjects with atopic dermatitis and 14,992 controls in the Japanese population, we report here 8 new susceptibility loci: IL1RL1-IL18R1-IL18RAP (P(combined) = 8.36 × 10(-18)), the major histocompatibility complex (MHC) region (P = 8.38 × 10(-20)), OR10A3-NLRP10 (P = 1.54 × 10(-22)), GLB1 (P = 2.77 × 10(-16)), CCDC80 (P = 1.56 × 10(-19)), CARD11 (P = 7.83 × 10(-9)), ZNF365 (P = 5.85 × 10(-20)) and CYP24A1-PFDN4 (P = 1.65 × 10(-8)).
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
GeneRIF
Consortium of Investigators of Modifiers of BRCA1/2 et al., Rochester, United States. In Cancer Epidemiol Biomarkers Prev, 2012
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
Variants in ZNF365 isoform D are associated with Crohn's disease.
GeneRIF
Taylor et al., Los Angeles, United States. In Gut, 2011
the non-synonymous Ala62Thr SNP, rs7076156, underlies the association between 10q21 and CD risk and suggest that this SNP acts by altering expression of genes under the control of ZNF365 isoform D.
Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies.
Review
Lai et al., China. In Breast Cancer Res Treat, 2011
Of the 25 SNPs, 20 were noteworthy: C6orf97 (rs2046210 and rs3757318), FGFR2 (rs2981579, rs1219648, and rs2981582), LSP1 (rs909116), RNF146 (rs2180341), SLC4A7 (rs4973768), MRPS30 (rs7716600), TOX3 (rs3803662 and rs4784227), ZNF365 (rs10995190), rs889312, rs614367, rs13281615, rs13387042, rs11249433, rs1011970, rs614367, and rs1562430.
Common variants in ZNF365 are associated with both mammographic density and breast cancer risk.
Impact
Tamimi et al., Boston, United States. In Nat Genet, 2011
We conducted a meta analysis of five genome-wide association studies of percent mammographic density and report an association with rs10995190 in ZNF365 (combined P = 9.6 × 10(-10)).
Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder.
GeneRIF
Mori et al., Hamamatsu, Japan. In Am J Med Genet B Neuropsychiatr Genet, 2009
The association of PCNT2 and DBZ with schizophrenia and bipolar disorder in a case-control study of Japanese cohorts, was examined.
Centrosomal proteins Nde1 and Su48 form a complex regulated by phosphorylation.
GeneRIF
Greene et al., Philadelphia, United States. In Oncogene, 2006
findings indicate that Su48 can form a protein complex with Nde1 in the centrosome and plays an important role for successful mitosis
[Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis].
Review
Esposito et al., Avellino, Italy. In Minerva Med, 2005
Uric acid nephrolithiasis (UAN) accounts for 20% of all stones but its prevalence varies between countries.
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate.
GeneRIF
Pirastu et al., Alghero, Italy. In Am J Hum Genet, 2003
A novel gene responsible for UAN was identified in an Italian population.
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