Varaico: Literature-Extracted Genetic Variants

Gene:CEP135
Variant:p.S997L
Back to variants list

CEP135

NM_025009.5:p.S997L

Associated Papers

Analysis of the "centrosome-ome" identifies MCPH1 deletion as a cause of centrosome amplification in human cancer.

Denu RA et al.

Scientific Reports, 2020

32681070 (PubMed )
Supplement: 41598_2020_68629_MOESM2_ESM.xlsx › Supp_Table_4

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_MOESM2_ESM.xlsx › S2

Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization.

Bizet AA et al.

Nature Communications, 2015

26487268 (PubMed )
Supplement: ncomms9666-s1.pdf

Bioinformatics analysis of thousands of TCGA tumors to determine the involvement of epigenetic regulators in human cancer.

Gnad F et al.

Bmc Genomics, 2015

26110843 (PubMed )
Supplement: 1471-2164-16-S8-S5-S7.xls › RecurrentMutations
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."