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GM01704 Fibroblast

Description:

GALACTOSEMIA
GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT

Affected:

Yes

Sex:

Male

Age:

2 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images
  • 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 2
Relation to Proband cousin
Confirmation Molecular characterization after cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks 2nd generation with transferase deficiency galactosemia; GALT gene mutation is [Gln188Arg (Q188R)]/?; 2nd allele is negative for R333W and N314D

Characterizations

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Passage Frozen 3
 
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
 
Gene GALT
Chromosomal Location 9p13
Allelic Variant 1 606999.0006; GALACTOSEMIA
Identified Mutation GLN188ARG; Reichardt et al. [Am J Hum Genet 49: 860 (1991)] demonstrated a transition at nucleotide 591 that substituted arginine for glutamine-188. The mutated glutamine is not only highly conserved in evolution, but is also 2 amino acid residues downstream from the active site histidine-proline-histidine triad. Lymphoblasts from subjects homozygous for the GLN188ARG mutation show essentially no detectable GALT activity [Fridovich-Keil and Jinks-Robertson. Proc Nat Acad Sci USA 90: 398 (1993)].

Phenotypic Data

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Remarks 2nd generation with transferase deficiency galactosemia; GALT gene mutation is [Gln188Arg (Q188R)]/?; 2nd allele is negative for R333W and N314D

Publications

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Janes V, Grabany S, Delbrouck J, Vincent SP, Gottschalk J, Elling L, Hanisch FG, Fluorinated Galactoses Inhibit Galactose-1-Phosphate Uridyltransferase and Metabolically Induce Galactosemia-like Phenotypes in HEK-293 Cells Cells9: 2020
PubMed ID: 32138379

External Links

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dbSNP dbSNP ID: 14673
Gene Cards GALT
Gene Ontology GO:0003982 UTP-hexose-1-phosphate uridylyltransferase activity
GO:0006012 galactose metabolism
GO:0008108 UDP-glucose-hexose-1-phosphate uridylyltransferase activity
GO:0016740 transferase activity
NCBI Gene Gene ID:2592
NCBI GTR 230400 GALACTOSEMIA I; GALAC1
606999 GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT
OMIM 230400 GALACTOSEMIA I; GALAC1
606999 GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT
Omim Description GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCY
  GALACTOSEMIA
  GALT DEFICIENCYGALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE; GALT, INCLUDED

Images

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View pedigree 

Culture Protocols

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Passage Frozen 3
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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$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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