Varaico: Literature-Extracted Genetic Variants

Gene:CCDC92
Variant:p.S70C
Back to variants list

CCDC92

NM_025140.3:p.S70C

Associated Papers

Integrated Cross-Platform Analysis Reveals Candidate Variants and Linkage Disequilibrium-Defined Loci Associated with Osteoporosis in Korean Postmenopausal Women.

Kim SK et al.

Diagnostics (basel, Switzerland), 2026

An integrative framework to prioritize genes in more than 500 loci associated with body mass index.

Hemerich D et al.

American Journal of Human Genetics, 2024

38754426 (PubMed )
Supplement: mmc2.xlsx › Table_S3

Genetic ablation of diabetes-associated gene Ccdc92 reduces obesity and insulin resistance in mice.

Ren L et al.

Iscience, 2023

High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune profile, clinical outcome and sensitivity to targeted therapies.

Toulmonde M et al.

Ebiomedicine, 2020

33254023 (PubMed )
Supplement: mmc5.xlsx › UPS_somatic_mutations_filtered

Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.

Vujkovic M et al.

Nature Genetics, 2020

32541925 (PubMed )
Supplement: NIHMS1589535-supplement-1589535_Supp_Tab1-26.xlsx › T14

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

Fragoza R et al.

Nature Communications, 2019

31515488 (PubMed )
Supplement: 41467_2019_11959_MOESM11_ESM.xlsx › SD7_-_Drug_Targets

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.

Justice AE et al.

Nature Genetics, 2019

30778226 (PubMed )
Supplement: NIHMS1016010-supplement-SupplementaryData17.xlsx › SD17._VEP_annotation

Regional fat depot masses are influenced by protein-coding gene variants.

Neville MJ et al.

Plos One, 2019

Structural Capacitance in Protein Evolution and Human Diseases.

Li C et al.

Journal of Molecular Biology, 2018

Association between single nucleotide polymorphism rs11057401 of CCDC92 gene and the risk of coronary heart disease (CHD).

Xiao L et al.

Lipids in Health and Disease, 2018

Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.

Lu X et al.

Nature Genetics, 2017

29083407 (PubMed )
Supplement: NIHMS909133-supplement-2.xlsx › Supplementary_Table_11

Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease.

Klarin D et al.

Nature Genetics, 2017

Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.

Ryu GM et al.

Nucleic Acids Research, 2009

19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeI-
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."