Varaico: Literature-Extracted Genetic Variants

Gene:DCDC2
Variant:p.P152A
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DCDC2

NM_016356.5:p.P152A

Associated Papers

Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations.

Sprissler R et al.

Cancers, 2020

32570879 (PubMed )
Supplement: cancers-12-01618-s001.zip › cancers-817200-Supplementary_Materials3 › Supplementary_table_S1.xlsx › TSG

iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors.

Melguizo-Sanchis D et al.

Cell Death & Disease, 2018

29374141 (PubMed )
Supplement: 41419_2017_141_MOESM8_ESM.xlsx › SAA1_Deleterious_Hits

Doublecortin domain containing protein 2 (DCDC2) genetic variants in primary sclerosing cholangitis.

Cheung AC et al.

Journal of Hepatology, 2017

Reply to: "Doublecortin domain containing protein 2 (DCDC2) genetic variants in primary sclerosing cholangitis".

Grammatikopoulos T et al.

Journal of Hepatology, 2017

Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.

Venkatesh SK et al.

Journal of Human Genetics, 2013

An examination of candidate gene SNPs for dyslexia in an Indian sample.

Venkatesh SK et al.

Behavior Genetics, 2011

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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."