ID

45608

Beschrijving

Principal Investigator: Joshua D. Milner, MD, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA MeSH: Dermatitis, Atopic,Asthma,Food Hypersensitivity,Skin Diseases, Infectious https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001369 We described five patients from four unrelated families who had severe atopic dermatitis and susceptibility to mild skin viral infections. Some patients also exhibited other allergic symptoms such as asthma and food allergy. We performed targeted sequencing for affected patients A-I of family A and B-I of family B, whole exome sequencing for D-I, D-II.1 and healthy mother D-II.3 of family D, and whole genome sequencing for C-I and healthy mother C-II.2 of family C. We identified three different novel damaging missense mutations of CARD11 (GeneID:84433) in patients A-I (L194P), B-I (R975W), and C-I (E57D). In patients D-I and D-II.1, a dup183_196 (p.K196_V197insMKEERDSYNDELVK) mutation was found in the coil-coil domain of the protein. These mutations act as dominant negatives impeding the scaffolding function of the wild type protein, which leads to downstream NF-kB and mTORC1 signaling defects after TCR stimulation. Sanger sequencing later identified the corresponding CARD11 mutations in the affected family members (C-II.1, D-II.2) that are not included in the dbGaP submission. Hypomorphic CARD11 dominant negative mutants are novel causes of severe atopic disease.

Link

dbGaP study = phs001369

Trefwoorden

  1. 21-02-23 21-02-23 - Simon Heim
Houder van rechten

Joshua D. Milner, MD, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA

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21 februari 2023

DOI

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Licentie

Creative Commons BY 4.0

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dbGaP phs001369 Germline hypomorphic CARD11 mutations in severe atopic disease

Eligibility Criteria

Inclusion and exclusion criteria
Beschrijving

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
*Inclusion Criteria: * Families who had similar atopic features (non-syndromic) and mild infections were studied.
Beschrijving

*Inclusion Criteria: * Families who had similar atopic features (non-syndromic) and mild infections were studied.

Datatype

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0015576
UMLS CUI [1,3]
C0392707
UMLS CUI [1,4]
C2945599
UMLS CUI [1,5]
C3714514
DNA was available for use in whole genome or exome sequencing.
Beschrijving

Elig.phs001369.v1.p1.2

Datatype

boolean

Alias
UMLS CUI [1,1]
C0470187
UMLS CUI [1,2]
C0012854
UMLS CUI [1,3]
C3640076
UMLS CUI [1,4]
C3640077
Informed consent documentation was available.
Beschrijving

Elig.phs001369.v1.p1.3

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0920316
UMLS CUI [1,3]
C0470187

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
*Inclusion Criteria: * Families who had similar atopic features (non-syndromic) and mild infections were studied.
Item
*Inclusion Criteria: * Families who had similar atopic features (non-syndromic) and mild infections were studied.
boolean
C1512693 (UMLS CUI [1,1])
C0015576 (UMLS CUI [1,2])
C0392707 (UMLS CUI [1,3])
C2945599 (UMLS CUI [1,4])
C3714514 (UMLS CUI [1,5])
Elig.phs001369.v1.p1.2
Item
DNA was available for use in whole genome or exome sequencing.
boolean
C0470187 (UMLS CUI [1,1])
C0012854 (UMLS CUI [1,2])
C3640076 (UMLS CUI [1,3])
C3640077 (UMLS CUI [1,4])
Elig.phs001369.v1.p1.3
Item
Informed consent documentation was available.
boolean
C0021430 (UMLS CUI [1,1])
C0920316 (UMLS CUI [1,2])
C0470187 (UMLS CUI [1,3])

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