ID

45985

Descrizione

Principal Investigator: Nicholas O. Davidson, MD, Washington University, St. Louis, MO, USA MeSH: Familial Adenomatous Polyposis,Colonic Neoplasms https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000904 The ~80% of individuals with classic familial adenomatous polyposis (FAP) have detectable mutations in the coding sequence of the adenomatous polyposis coli (APC) gene. To investigate the 20% of families without detectable causative mutations, we used exome sequencing and second-generation sequencing of the APC locus including non-coding regions. We identified a novel ~11kb deletion 44kb upstream of APC that was present only in affected individuals of three kindreds. SNP analysis showed that this ~11kb deletion was accompanied by silencing of one of the APC alleles in blood-derived RNA of affected individuals.

collegamento

dbGaP study=phs000904

Keywords

  1. 06/04/24 06/04/24 - Madita Rudolph
Titolare del copyright

Nicholas O. Davidson, MD, Washington University, St. Louis, MO, USA

Caricato su

6 aprile 2024

DOI

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Licenza

Creative Commons BY 4.0

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dbGaP phs000904 APC Promoter Deletion in Classic Familial Adenomatous Polyposis

Eligibility Criteria

Inclusion and exclusion criteria
Descrizione

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
*Inclusion Criteria:* Individuals with classic familial adenomatous polyposis were tested for known APC mutations with Colaris AP® (Myriad Genetic Laboratories). Those without detectable mutations by Colaris AP® and consenting family members were enrolled.
Descrizione

Elig.phs000904.v1.p1.1

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0032580
UMLS CUI [1,3]
C4522286
UMLS CUI [1,4]
C0039593
UMLS CUI [2,1]
C1512693
UMLS CUI [2,2]
C0021430
UMLS CUI [2,3]
C0086282
*Exclusion Criteria:* Individuals with sporadic gastrointestinal cancer or a family history of cancer not suggestive of hereditary or familial diseases were excluded.
Descrizione

Elig.phs000904.v1.p1.2

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0685938
UMLS CUI [1,3]
C0205422
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C0260515
UMLS CUI [2,3]
C0019247
UMLS CUI [2,4]
C1272460

Similar models

Eligibility Criteria

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000904.v1.p1.1
Item
*Inclusion Criteria:* Individuals with classic familial adenomatous polyposis were tested for known APC mutations with Colaris AP® (Myriad Genetic Laboratories). Those without detectable mutations by Colaris AP® and consenting family members were enrolled.
boolean
C1512693 (UMLS CUI [1,1])
C0032580 (UMLS CUI [1,2])
C4522286 (UMLS CUI [1,3])
C0039593 (UMLS CUI [1,4])
C1512693 (UMLS CUI [2,1])
C0021430 (UMLS CUI [2,2])
C0086282 (UMLS CUI [2,3])
Elig.phs000904.v1.p1.2
Item
*Exclusion Criteria:* Individuals with sporadic gastrointestinal cancer or a family history of cancer not suggestive of hereditary or familial diseases were excluded.
boolean
C0680251 (UMLS CUI [1,1])
C0685938 (UMLS CUI [1,2])
C0205422 (UMLS CUI [1,3])
C0680251 (UMLS CUI [2,1])
C0260515 (UMLS CUI [2,2])
C0019247 (UMLS CUI [2,3])
C1272460 (UMLS CUI [2,4])

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