Varaico: Literature-Extracted Genetic Variants

Gene:CENPE
Variant:p.K1355E
Back to variants list

CENPE

NM_001813.3:p.K1355E

Associated Papers

A non-canonical function for Centromere-associated protein-E controls centrosome integrity and orientation of cell division.

Owa M et al.

Communications Biology, 2021

Kinesin-7 CENP-E regulates cell division, gastrulation and organogenesis in development.

Yu KW et al.

European Journal of Cell Biology, 2020

Systematic analysis of the intersection of disease mutations with protein modifications.

Simpson CM et al.

Bmc Medical Genomics, 2019

31345222 (PubMed )
Supplement: 12920_2019_543_MOESM6_ESM.xlsx › S5C

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Rivas MA et al.

Plos Genetics, 2018

29795570 (PubMed )
Supplement: pgen.1007329.s012.xlsx › Data_File_S3

Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.

Nava C et al.

Amino Acids, 2015

26215737 (PubMed )
Supplement: 726_2015_2057_MOESM2_ESM.xlsx › Sup_Table_3

De novo mutations in moderate or severe intellectual disability.

Hamdan FF et al.

Plos Genetics, 2014

25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1883.659

Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism.

Mirzaa GM et al.

Human Genetics, 2014

Computational screening and molecular dynamics simulation of disease associated nsSNPs in CENP-E.

Kumar A et al.

Mutation Research, 0

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."