Varaico: Literature-Extracted Genetic Variants

Gene:PRKN
Variant:p.C182*
Back to variants list

PRKN

NM_004562.3:p.C182*

Associated Papers

Comparison of TP53 mutations in myelodysplasia and acute leukemia suggests divergent roles in initiation and progression.

Jambhekar A et al.

Blood Neoplasia, 2024

40453522 (PubMed )
Supplement: BNEO_NEO-2023-000115-mmc1.xlsx › MDS

SNRPD2 Is a Novel Substrate for the Ubiquitin Ligase Activity of the Salmonella Type III Secretion Effector SlrP.

Bullones-Bolaños A et al.

Biology, 2022

Lysosomal defects in ATP13A2 and GBA associated familial Parkinson's disease.

Sato S et al.

Journal of Neural Transmission (vienna, Austria : 1996), 2017

Aurora B kinase is a potent and selective target in MYCN-driven neuroblastoma.

Bogen D et al.

Oncotarget, 2015

HTRA2 variations in Taiwanese Parkinson's disease.

Chen CM et al.

Journal of Neural Transmission (vienna, Austria : 1996), 2014

Mutations in the ATP13A2 gene and Parkinsonism: a preliminary review.

Yang X et al.

Biomed Research International, 2014

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."