Varaico: Literature-Extracted Genetic Variants

Gene:C8G
Variant:p.P3H
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C8G

NM_000606.3:p.P3H

Associated Papers

Depletion of individual dietary amino acids induce distinct metabolic and chromatin states.

Haws SA et al.

The Journal of Biological Chemistry, 2025

41419194 (PubMed )
Supplement: mmc4.xlsx › Shared_EAA_DE_GO-BP_Enrichment

Germline pathogenic variation impacts somatic alterations and patient outcomes in pediatric central nervous system tumors.

Corbett RJ et al.

Nature Communications, 2025

41271695 (PubMed )
Supplement: 41467_2025_65190_MOESM12_ESM.xlsx › S10C_KEGG_pathways

Germline pathogenic variation impacts somatic alterations and patient outcomes in pediatric CNS tumors.

Corbett RJ et al.

Medrxiv : the Preprint Server for Health Sciences, 2025

39974082 (PubMed )
Supplement: media-11.xlsx › S10C_KEGG_pathways

Multiomic approach and Mendelian randomization analysis identify causal associations between blood biomarkers and subcortical brain structure volumes.

Jain PR et al.

Neuroimage, 2023

37995919 (PubMed )
Supplement: NIHMS1949324-supplement-2.zip › Additional_File_2.xlsx › Amygdala

Multiomic approach and Mendelian randomization analysis identify causal associations between blood biomarkers and subcortical brain structure volumes.

Jain P et al.

Medrxiv : the Preprint Server for Health Sciences, 2023

37066330 (PubMed )
Supplement: media-1.zip › Additional_File_2.xlsx › Amygdala

IGF1 deficiency integrates stunted growth and neurodegeneration in Down syndrome.

Araya P et al.

Cell Reports, 2022

36577365 (PubMed )
Supplement: NIHMS1861170-supplement-6.xlsx › A._SOMAscan_prot._T21_vs._D21

Proteomic Landscape of Exosomes Reveals the Functional Contributions of CD151 in Triple-Negative Breast Cancer.

Li S et al.

Molecular & Cellular Proteomics : Mcp, 2021

34265469 (PubMed )
Supplement: mmc7.xlsx › Enrichment

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases.

Zheng J et al.

Nature Genetics, 2020

32895551 (PubMed )
Supplement: EMS118445-supplement-Supplementary_Tables.xlsx › TableS1.Instruments

Novel CSF biomarkers in genetic frontotemporal dementia identified by proteomics.

van der Ende EL et al.

Annals of Clinical and Translational Neurology, 2019

31019994 (PubMed )
Supplement: ACN3-6-698-s003.xlsx › Enriched_GO_terms

The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance.

Conte I et al.

Nucleic Acids Research, 2014

24895435 (PubMed )
Supplement: supp_gku498_nar-02440-y-2013-File009.xlsx › Supp_Table_2

The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.

Dewald G et al.

Annals of Human Genetics, 1996

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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."