Varaico: Literature-Extracted Genetic Variants

Gene:PRH2
Variant:p.L19I
Back to variants list

PRH2

NM_001110213.1:p.L19I

Associated Papers

Mutation Analysis of DNAJC Family for Early-Onset Parkinson's Disease in a Chinese Cohort.

Li C et al.

Movement Disorders : Official Journal of the Movement Disorder Society, 2020

Discovery of new potentially defective alleles of human CYP2C9.

Blaisdell J et al.

Pharmacogenetics, 2004

Thrombin interacts with thrombomodulin, protein C, and thrombin-activatable fibrinolysis inhibitor via specific and distinct domains.

Hall SW et al.

The Journal of Biological Chemistry, 1999

ADP ribosylation factor 1 mutants identify a phospholipase D effector region and reveal that phospholipase D participates in lysosomal secretion but is not sufficient for recruitment of coatomer I.

Jones DH et al.

The Biochemical Journal, 1999

Functional requirements for inhibition of thrombin by antithrombin III in the presence and absence of heparin.

Tsiang M et al.

The Journal of Biological Chemistry, 1997

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."