Associated Papers
Functional characterization of C21ORF2 association with the NEK1 kinase mutated in human in diseases.
Gregorczyk M et al.
Life Science Alliance, 2023
Prediction of structural consequences for disease causing variants in C21orf2 protein using computational approaches.
Iyer S et al.
Journal of Biomolecular Structure & Dynamics, 2019
Exome-wide Association Study Identifies CLEC3B Missense Variant p.S106G as Being Associated With Extreme Longevity in East Asian Populations.
Tanisawa K et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2017
27154906 (PubMed )
Supplement: glw074_suppl_20160228_jgbs_2015_218r1_supplemantary_tables.xlsx › Table_S3
Extended haplotype association study in Crohn's disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3.
Zhang W et al.
Genes and Immunity, 0
23615072 (PubMed )
Supplement: NIHMS458938-supplement-1.xls › Supplemental_table_3
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