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GM05002 Fibroblast

Description:

GLUTARICACIDEMIA I

Affected:

Yes

Sex:

Male

Age:

2 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
Cell Type Fibroblast
Transformant Untransformed
Race White
Ethnicity IRISH
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Delayed motor & mental development, dystonia, spasticity, choreoathetosis, & metabolic acidosis; deficient glutarylCoA dehydrogenase activity; negative family history; donor subject is a compound heterozygote: one allele has a G>A transition at nucleotide 344 in exon 5 of the GCDH gene (C.344G>A) resulting in the substitution of tyrosine for cysteine at codon 115 [Cys115Tyr (C115Y)]; and the second allele has a C>T transition at nucleotide 743 in exon 7 (c.743C>T) resulting in a substitution of leucine for proline at codon 248 [Pro248Leu (P248L)]

Characterizations

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Passage Frozen 6
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis
 
glutaryl-CoA dehydrogenase According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 1.3.99.7
 
glutaryl-CoA dehydrogenase According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 1.3.99.7
 
Gene GCDH
Chromosomal Location 19p13.2
Allelic Variant 1 C115Y; GLUTARICACIDEMIA I
Identified Mutation CYS115TYR
 
Gene GCDH
Chromosomal Location 19p13.2
Allelic Variant 2 P248L; GLUTARICACIDEMIA I
Identified Mutation PRO248LEU

Phenotypic Data

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Remarks Delayed motor & mental development, dystonia, spasticity, choreoathetosis, & metabolic acidosis; deficient glutarylCoA dehydrogenase activity; negative family history; donor subject is a compound heterozygote: one allele has a G>A transition at nucleotide 344 in exon 5 of the GCDH gene (C.344G>A) resulting in the substitution of tyrosine for cysteine at codon 115 [Cys115Tyr (C115Y)]; and the second allele has a C>T transition at nucleotide 743 in exon 7 (c.743C>T) resulting in a substitution of leucine for proline at codon 248 [Pro248Leu (P248L)]

Publications

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Leibel RL, Shih VE, Goodman SI, Bauman ML, McCabe ER, Zwerdling RG, Bergman I, Costello C, Glutaric acidemia: a metabolic disorder causing progressive choreoathetosis. Neurology30:1163-8 1980
PubMed ID: 6775244

External Links

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dbSNP dbSNP ID: 21186
NCBI GTR 231670 GLUTARIC ACIDEMIA I; GA1
OMIM 231670 GLUTARIC ACIDEMIA I; GA1
Omim Description GA I
  GLUTARICACIDEMIA I
  GLUTARICACIDURIA I
  GLUTARYL-CoA DEHYDROGENASE DEFICIENCYGLUTARYL-CoA DEHYDROGENASE, INCLUDED; GCDH, INCLUDED

Culture Protocols

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Passage Frozen 6
Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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