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GM00054 Fibroblast

Description:

GALACTOSEMIA

Affected:

Yes

Sex:

Male

Age:

3 MO (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 Carbohydrate Metabolism
Cell Type Fibroblast
Transformant Untransformed
Race White
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks See also GM00638A (SV40 Transformed) and GM02795A Lymphoid; G6PD type B; same patient as GM01907; deficient transferase and normal kinase activity in fibroblasts

Characterizations

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Passage Frozen 10
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis
 
UDP-glucose--hexose-1-phosphate uridylyltransferase According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 2.7.7.12
 

Phenotypic Data

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Remarks See also GM00638A (SV40 Transformed) and GM02795A Lymphoid; G6PD type B; same patient as GM01907; deficient transferase and normal kinase activity in fibroblasts

Publications

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Lai K, Langley SD, Khwaja FW, Schmitt EW, Elsas LJ, GALT deficiency causes UDP-hexose deficit in human galactosemic cells Glycobiology13:285-94 2003
PubMed ID: 12626383
 
Day RS 3d, Ziolkowski CH, Scudiero DA, Meyer SA, Lubiniecki AS, Girardi AJ, Galloway SM, Bynum GD, Defective repair of alkylated DNA by human tumour and SV40-transformed human cell strains. Nature288:724-7 1980
PubMed ID: 6256643
 
Tedesco TA, Miller KL, Galactosemia: alterations in sulfate metabolism secondary to galactose- 1-phosphate uridyltransferase deficiency. Science205:1395-7 1979
PubMed ID: 472754
 
Chen YT, Worthy TE, Krooth RS, Evidence for a striking increase in acetylcholinesterase activity in cultured human fibroblasts which are trisomic for chromosome two. Somatic Cell Genet4:265-98 1978
PubMed ID: 694721
 
Greene AE, Manduka M, Coriell LL, SV40 virus transformation of genetic mutant cell cultures. Monogr Hum Genet9:248-52 1978
PubMed ID: 215903
 
Croce CM, Assignment of the integration site for simian virus 40 to chromosome 17 in GM54VA, a human cell line transformed by simian virus 40. Proc Natl Acad Sci U S A74:315-8 1977
PubMed ID: 189310
 
Friedman TB, Yarkin RJ, Merril CR, Galactose and glucose metabolism in galactokinase deficient, galactose- 1-P-uridyl transferase deficient and normal human fibroblasts. J Cell Physiol85:569-78 1975
PubMed ID: 167035

External Links

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dbSNP dbSNP ID: 19634
NCBI GTR 230400 GALACTOSEMIA I; GALAC1
OMIM 230400 GALACTOSEMIA I; GALAC1
Omim Description GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCY
  GALACTOSEMIA
  GALT DEFICIENCYGALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE; GALT, INCLUDED

Culture Protocols

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Passage Frozen 10
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 -
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International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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