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GM23597 LCL from B-Lymphocyte

Description:

ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO; OTC
ORNITHINE CARBAMOYLTRANSFERASE; OTC

Affected:

At Risk

Sex:

Female

Age:

36 YR (At Sampling)

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Disorders of the Urea Cycle
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race Asian
Ethnicity Not Hispanic/Latino
Country of Origin USA
Family History Y
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Asymptomatic; donor subject is heterozygous for a G>A transition at nucleotide 119 in exon 2 of the OTC gene (c.119G>A) resulting in the substitution of histidine for arginine at codon 40 [Arg40His (R40H)]; positive family history.

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene OTC
Chromosomal Location Xp21.1
Allelic Variant 1 300461.0029; OTC DEFICIENCY
Identified Mutation ARG40HIS; Mavinakere et al. (2001) used (35)S labeling to study import and processing of OTC carrying the R40H mutation in intact CHO cells and in isolated rat liver mitochondria compared to wildtype and OTC carrying an R141Q mutant that causes complete enzyme deficiency. OTC protein carrying the R40H mutation seemed to be imported and processed by the mitochondria in a manner similar to that of wildtype. However, it was consistently degraded to a smaller fragment in the intact cells, unlike the wildtype and R141Q mutant. The mature form of the enzyme was not susceptible to degradation. Mavinakere et al. (2001) concluded that deficiency in OTC enzymatic function conferred by the R40H mutation is likely caused by enhanced degradation of the preprotein in the cytosol. The authors further proposed that the variation in the rate of OTC turnover is responsible for the heterogeneity of the clinical phenotype in patients carrying this mutation.

Phenotypic Data

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Remarks Asymptomatic; donor subject is heterozygous for a G>A transition at nucleotide 119 in exon 2 of the OTC gene (c.119G>A) resulting in the substitution of histidine for arginine at codon 40 [Arg40His (R40H)]; positive family history.

External Links

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Gene Cards OTC
Gene Ontology GO:0000050 urea cycle
GO:0004585 ornithine carbamoyltransferase activity
GO:0005759 mitochondrial matrix
GO:0006520 amino acid metabolism
GO:0006526 arginine biosynthesis
GO:0009348 ornithine carbamoyltransferase complex
GO:0016597 amino acid binding
GO:0016740 transferase activity
NCBI Gene Gene ID:5009
NCBI GTR 300461 ORNITHINE CARBAMOYLTRANSFERASE; OTC
311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO
OMIM 300461 ORNITHINE CARBAMOYLTRANSFERASE; OTC
311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO
Omim Description OCT DEFICIENCY; OCTDORNITHINE CARBAMOYLTRANSFERASE, INCLUDED; OTC, INCLUDED
  ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY
  ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO; OTC
  VALPROATE SENSITIVITY, INCLUDED

Culture Protocols

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Split Ratio 1:3
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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