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GM22194 LCL from B-Lymphocyte

Description:

BARTH SYNDROME; BTHS
TAFAZZIN; TAZ

Affected:

Yes

Sex:

Male

Age:

9 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Ethnicity DUTCH/SCOTTISH
Family History N
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Clinically affected; one affected maternal nephew; family history of spontaneous abortions; 3-methylglutaconic aciduria; failure to thrive; neutropenia; donor subject has a complete deletion of the TAZ (G4.5) gene

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin confirmed by LINE assay
 
Gene TAZ
Chromosomal Location Xq28
Allelic Variant 1 ; BARTH SYNDROME
Identified Mutation COMPLETE DELETION

Phenotypic Data

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Remarks Clinically affected; one affected maternal nephew; family history of spontaneous abortions; 3-methylglutaconic aciduria; failure to thrive; neutropenia; donor subject has a complete deletion of the TAZ (G4.5) gene

Publications

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Chan JZ, Fernandes MF, Steckel KE, Bradley RM, Hashemi A, Groh MR, Sciaini G, Stark KD, Duncan RE, N-oleoylethanolamide treatment of lymphoblasts deficient in Tafazzin improves cell growth and mitochondrial morphology and dynamics Scientific reports12:9466 2022
PubMed ID: 35676289
 
Zegallai HM, Hatch GM, Impaired surface marker expression in stimulated Epstein-Barr virus transformed lymphoblasts from Barth Syndrome patients Scientific reports12:6195 2022
PubMed ID: 35418665
 
Ghosh S, Basu Ball W, Madaris TR, Srikantan S, Madesh M, Mootha VK, Gohil VM, An essential role for cardiolipin in the stability and function of the mitochondrial calcium uniporter Proceedings of the National Academy of Sciences of the United States of America12:6195 2020
PubMed ID: 32601238

External Links

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Gene Cards TAZ
Gene Ontology GO:0006936 muscle contraction
GO:0007507 heart development
GO:0007517 muscle development
GO:0008152 metabolism
GO:0008415 acyltransferase activity
GO:0016021 integral to membrane
NCBI Gene Gene ID:6901
NCBI GTR 300394 TAFAZZIN; TAZ
302060 BARTH SYNDROME; BTHS
OMIM 300394 TAFAZZIN; TAZ
302060 BARTH SYNDROME; BTHS
Omim Description 3-@METHYLGLUTACONICACIDURIA, TYPE II
  BARTH SYNDROME; BTHS
  CARDIOSKELETAL MYOPATHY WITH NEUTROPENIA AND ABNORMAL MITOCHONDRIA
  ENDOCARDIAL FIBROELASTOSIS 2; EFE2
  ISOLATED NONCOMPACTION OF THE LEFT VENTRICLE MYOCARDIUM, INCLUDED;INVM, INCLUDED
  MGA, TYPE IITAFAZZIN, INCLUDED; TAZ, INCLUDED

Culture Protocols

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Split Ratio 1:5
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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