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GM02292 LCL from B-Lymphocyte

Description:

LESCH-NYHAN SYNDROME; LNS

Affected:

Yes

Sex:

Male

Age:

19 FW (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 Nucleotide and Nucleic Acid Metabolism
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Ethnicity ENGLISH
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Similarly affected brother; see GM02290A & GM02291 Fibroblast & GM02338 Amniotic; nonviable in HAT medium; no detectable stable HPRT mRNA

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
 
hypoxanthine phosphoribosyltransferase Lymphoblasts are nonviable in HAT medium and have no detectable stable HPRT mRNA (Yang et al Nature 310:412 1984). Monnat (Cancer Res 49:8187 1989) used this cell culture as an HPRT negative and HPRT mRNA negative control in respective enzyme activity assays and in Northern analyses. EC Number: 2.4.2.8; 0% activity.
 

Phenotypic Data

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Remarks Similarly affected brother; see GM02290A & GM02291 Fibroblast & GM02338 Amniotic; nonviable in HAT medium; no detectable stable HPRT mRNA

Publications

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Caballero M, Ge T, Rebelo AR, Seo S, Kim S, Brooks K, Zuccaro M, Kanagaraj R, Vershkov D, Kim D, Smogorzewska A, Smolka M, Benvenisty N, West SC, Egli D, Mace EM, Koren A, Comprehensive analysis of DNA replication timing across 184 cell lines suggests a role for MCM10 in replication timing regulation Human molecular genetics: 2021
PubMed ID: 35394024
 
Dittmann KH, Dikomey E, Mayer C, Rodemann HP, The Bowman-Birk protease inhibitor enhances clonogenic cell survival of ionizing radiation-treated nucleotide excision repair-competent cells but not of xeroderma pigmentosum cells. Int J Radiat Biol76(2):223-9 2000
PubMed ID: 10716643
 
Monnat RJ Jr, Molecular analysis of spontaneous hypoxanthine phosphoribosyltransferase mutations in thioguanine-resistant HL-60 human leukemia cells. Cancer Res49:81-7 1989
PubMed ID: 2908855
 
Yang TP, Patel PI, Chinault AC, Stout JT, Jackson LG, Hildebrand BM, Caskey CT, Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients. Nature310:412-4 1984
PubMed ID: 6087154
 
Tischfield J, Schafer IA, Dickerman LH, Trill J, Mulivor RA, Greene AE, Coriell LL, Lesch-Nyhan syndrome. Repository identification Nos. GM-2290, 2291, 2292, 2338, 3115, 3116, and 3117. Cytogenet Cell Genet24:199-200 1979
PubMed ID: 477417

External Links

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dbSNP dbSNP ID: 21193
NCBI GTR 300322 LESCH-NYHAN SYNDROME; LNS
OMIM 300322 LESCH-NYHAN SYNDROME; LNS
Omim Description LESCH-NYHAN SYNDROME; LNS

Images

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View pedigree 

Culture Protocols

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Split Ratio 1:3
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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