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Functional evaluation of PTEN missense mutations using in vitro phosphoinositide phosphatase assay.

Authors not recorded

Cancer Res2000PMID 10866302stubpubmedProvenance
Source
PubMed
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-CIVIC-20260908-000001
Published

Abstract

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Linked entities

Linked entities (3)

How each link was made (MeSH, dictionary, registry reference, curation…) and whether it has been validated. Candidate links are not counted in entity statistics.

Validated 3

Curated evidence

Evidence citing this paper (2)

civicProvenance
Source
CIViC — Clinical Interpretation of Variants in Cancer
Dataset
CIViC evidence items
Version
civic-2026-09-08
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Evidence
expert curation
License
CC0 1.0
PMID
10866302
Run
ING-CIVIC-20260908-000001
Open at source
CuratedShowing 1–2 of 2 evidence items · levels, directions and significance as curated at the source; each row links to its CIViC record.
TherapyCancerTypeLevelDirection · significanceRating (1–5)StatusEvidenceSource
PTEN R173C1
(predisposing)Malignant NeoplasmALIASPredisposingDSupports Uncertain Significance3accepted
EID1930

Han et al functionally tested the R173C mutation in PTEN using an expression vector construct, assessing phosphatase activity of the mutant construct with two phosphoinositide substrates ("with[ PtdIn… (full text at CIViC)

PMID 10866302 · Han et al., 2000 · Open in CIViC

civic
PTEN R130Q1
(functional)—UNRESOLVEDFunctionalDSupports Loss Of Function2submitted
EID7693

Missense mutations in PTEN were characterized for phosphatase activity and the ability to bind a phospholipid membrane. Phosphatase assays revealed that PTEN R130Q retains no phosphatase activity in v… (full text at CIViC)

PMID 10866302 · Han et al., 2000 · Open in CIViC

civic