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AG18465 LCL from B-Lymphocyte

Description:

ROTHMUND-THOMSON SYNDROME; RTS
RECQ PROTEIN-LIKE 4; RECQL4

Affected:

Yes

Sex:

Male

Age:

13 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images
  • Culture Protocols

Overview

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Repository NIA Aging Cell Culture Repository
Subcollection Heritable Diseases
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race Hispanic/Latino
Family Member 1
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
ISCN 47,XY,inv(9)(pter>p11::q13>p11::q13>qter),+11[3]/46,XY,inv(9)(pter>p11::q13>p11::q13>qter)[47]
Species Homo sapiens
Common Name Human
Remarks Clinically affected; donor has features of severe poikiloderma, small stature, skeletal abnormalities, and right cataract; the donor subject is homozygous for a truncating mutation in the RECQL4 gene: a C>T transition at nucleotide g.4503(g.4503C>T) in exon 14 which leads to truncation at codon 810 [GLN810TER (Q810X)]. The karyotype is 47,XY,inv(9)(p11q13),+11[3]/46,XY,inv(9)(p11q13)[47] with 8% of the cells examined showing random chromosome loss/gain. The legacy karyotype description shown in this Remark may not be representative of the current available product.

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
 
Gene RECQL4
Chromosomal Location 8q24.3
Allelic Variant 1 GLN810TER; ROTHMUND-THOMSON SYNDROME
Identified Mutation g.4503C>T
 
Gene RECQL4
Chromosomal Location 8q24.3
Allelic Variant 2 GLN810TER; ROTHMUND-THOMSON SYNDROME
Identified Mutation g.4503C>T

Phenotypic Data

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Remarks Clinically affected; donor has features of severe poikiloderma, small stature, skeletal abnormalities, and right cataract; the donor subject is homozygous for a truncating mutation in the RECQL4 gene: a C>T transition at nucleotide g.4503(g.4503C>T) in exon 14 which leads to truncation at codon 810 [GLN810TER (Q810X)]. The karyotype is 47,XY,inv(9)(p11q13),+11[3]/46,XY,inv(9)(p11q13)[47] with 8% of the cells examined showing random chromosome loss/gain. The legacy karyotype description shown in this Remark may not be representative of the current available product.

Publications

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Wang LL, Gannavarapu A, Kozinetz CA, Levy ML, Lewis RA, Chintagumpala MM, Ruiz-Maldanado R, Contreras-Ruiz J, Cunniff C, Erickson RP, Lev D, Rogers M, Zackai EH, Plon SE, Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome. J Natl Cancer Inst95(9):669-74 2003
PubMed ID: 12734318

External Links

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dbSNP dbSNP ID: 22295
Gene Cards RECQL4
RTS
Gene Ontology GO:0003676 nucleic acid binding
GO:0003678 DNA helicase activity
GO:0005524 ATP binding
GO:0005634 nucleus
GO:0006281 DNA repair
GO:0007275 development
GO:0008026 ATP-dependent helicase activity
GO:0016787 hydrolase activity
NCBI Gene Gene ID:9401
NCBI GTR 268400 ROTHMUND-THOMSON SYNDROME, TYPE 2; RTS2
603780 RECQ PROTEIN-LIKE 4; RECQL4
OMIM 268400 ROTHMUND-THOMSON SYNDROME, TYPE 2; RTS2
603780 RECQ PROTEIN-LIKE 4; RECQL4
Omim Description POIKILODERMA ATROPHICANS AND CATARACT
  ROTHMUND-THOMSON SYNDROME; RTS

Images

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View karyotype 
karyotype 

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
Commercial:
$257.00USD
Academic &
Non-profit:
$103.00USD
NIA Grantees:
$47.00USD
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How to Order
  • Ordering Instructions
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