Varaico: Literature-Extracted Genetic Variants

Gene:EMC1
Variant:p.R881C
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EMC1

NM_015047.3:p.R881C

Associated Papers

Structural and mechanistic basis of the EMC-dependent biogenesis of distinct transmembrane clients.

Miller-Vedam LE et al.

Elife, 2020

Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects.

Edwards JJ et al.

Jacc. Basic to Translational Science, 2020

32368696 (PubMed )
Supplement: mmc3.xlsx › Cases

Disrupted ER membrane protein complex-mediated topogenesis drives congenital neural crest defects.

Marquez J et al.

The Journal of Clinical Investigation, 2020

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.

Kosmicki JA et al.

Nature Genetics, 2017

28191890 (PubMed )
Supplement: NIHMS845776-supplement-5.xlsx › Congenital_Heart_Disease

Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies.

Tiwari A et al.

Scientific Reports, 2016

27353947 (PubMed )
Supplement: srep28755-s1.pdf
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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."