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GM01454 LCL from B-Lymphocyte

Description:

CYSTATHIONINURIA
CYSTATHIONINE GAMMA-LYASE; CTH

Affected:

Yes

Sex:

Male

Age:

7 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
Class Disorders of Amino Acid Metabolism
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race Asian
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Unresponsive to B6; HLA type A28,A2, Bw40,Bw21; 47,XY,+12/47,XY,+12,add(13) (q34); 48%/52%; random chromosome rearrangements are present; donor subject is homozygous for a 2 bp deletion at nucleotide 940 in exon 8 of the CTH gene (940_941delCT) resulting in the substitution of threonine for leucine at codon 262 {Leu262Thr (L262T)] causing a stop codon at 282

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Chromosome Analysis
 
Gene CTH
Chromosomal Location 1p31.1
Allelic Variant 1 607657.0001; CYSTATHIONINURIA
Identified Mutation 2 BP DEL, 940CT
 
Gene CTH
Chromosomal Location 1p31.1
Allelic Variant 2 607657.0001; CYSTATHIONINURIA
Identified Mutation 2 BP DEL, 940CT
Cytogenetics Chromosome 12: ANEUPLOID Aneuploid Segment (+)12pter>12qter
Chromosome 12: ANEUPLOID Trisomic Segment 12pter>12qter

Phenotypic Data

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Remarks Unresponsive to B6; HLA type A28,A2, Bw40,Bw21; 47,XY,+12/47,XY,+12,add(13) (q34); 48%/52%; random chromosome rearrangements are present; donor subject is homozygous for a 2 bp deletion at nucleotide 940 in exon 8 of the CTH gene (940_941delCT) resulting in the substitution of threonine for leucine at codon 262 {Leu262Thr (L262T)] causing a stop codon at 282

Publications

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Treff NR, Tao X, Ferry KM, Su J, Taylor D, Scott RT, Development and validation of an accurate quantitative real-time polymerase chain reaction-based assay for human blastocyst comprehensive chromosomal aneuploidy screening Fertility and sterility97:819-824.e2 2011
PubMed ID: 22342859
 
Wang J, Hegele RA, Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH). Hum Genet112(4):404-8 2003
PubMed ID: 12574942

External Links

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dbSNP dbSNP ID: 10403
Gene Cards CTH
Gene Ontology GO:0004123 cystathionine gamma-lyase activity
GO:0006520 amino acid metabolism
GO:0016829 lyase activity
GO:0019344 cysteine biosynthesis
NCBI Gene Gene ID:1491
NCBI GTR 219500 CYSTATHIONINURIA
607657 CYSTATHIONINE GAMMA-LYASE; CTH
OMIM 219500 CYSTATHIONINURIA
607657 CYSTATHIONINE GAMMA-LYASE; CTH
Omim Description CYSTATHIONINURIA
  GAMMA-CYSTATHIONASE DEFICIENCY; CTHCYSTATHIONINE-GAMMA-LYASE, INCLUDED

Culture Protocols

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Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
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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