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GM02473 LCL from B-Lymphocyte

Description:

XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD

Affected:

No

Sex:

Female

Age:

34 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 Nucleotide and Nucleic Acid Metabolism
Class Repair Defective and Chromosomal Instability Syndromes
Alternate IDs GM17154 [XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD]
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race Black/African American
Family Member 2
Relation to Proband mother
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically normal; 46,XX; 12% of cells show random chromosome loss

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis
 
MEX PHENOTYPES Sklar and Strauss (NATURE 289:417-420,1981) assigned this culture a mex- phenotype based upon its ability to remove O6-MeG from alkylated DNA.
 

Phenotypic Data

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Remarks Clinically normal; 46,XX; 12% of cells show random chromosome loss

Publications

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Johnson RT, Squires S, The XPD complementation group. Insights into xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy. Mutat Res273(2):97-118 1992
PubMed ID: 1372108
 
Teitz T, Eli D, Penner M, Bakhanashvili M, Naiman T, Timme TL, Wood CM, Moses RE, Canaani D, Expression of the cDNA for the beta subunit of human casein kinase II confers partial UV resistance on xeroderma pigmentosum cells. Mutat Res236:85-97 1990
PubMed ID: 1694965
 
Sklar R, Strauss B, Removal of O6-methylguanine from DNA of normal and xeroderma pigmentosum-derived lymphoblastoid lines. Nature289:417-20 1981
PubMed ID: 7464910

External Links

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dbSNP dbSNP ID: 10521
NCBI GTR 278730 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD
OMIM 278730 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD
Omim Description TRICHOTHIODYSTROPHY, TYPE 1, INCLUDED; TDD1, INCLUDED
  XERODERMA PIGMENTOSUM IV; XP4TRICHOTHIODYSTROPHY WITH SUN SENSITIVITY, INCLUDED
  XERODERMA PIGMENTOSUM VIII, FORMERLY; XP8, FORMERLY
  XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD
  XP, GROUP D; XPDC
  XP, GROUP H, FORMERLY; XPH, FORMERLY

Culture Protocols

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Split Ratio 1:4
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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