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GM06935 Fibroblast from Skin, Unspecified

Description:

FANCONI ANEMIA COMPLEMENTATION GROUP UNDETERMINED

Affected:

Yes

Sex:

Female

Age:

12 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 Repair Defective and Chromosomal Instability Syndromes
Biopsy Source Unspecified
Cell Type Fibroblast
Tissue Type Skin
Transformant Simian Virus 40
Sample Source Fibroblast from Skin, Unspecified
Race White
Ethnicity ARABIAN
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected; pancytopenia; brown patchy pigmentation on skin; untransformed fibroblasts are not sensitive to cell killing by mitomycin-C or diepoxybutane even at higher concentrations; modal number of chromosomes is 114, range is 106 to 122; structural aberrations & polyploidy; SV40 transformed GM02053.

Characterizations

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Passage Frozen 27
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Chromosome Analysis. DNA fingerprinting and HLA DQ-alpha typing showed that this SV40 transformed fibroblast culture had the same pattern and genotype as GM02053, the untransformed fibroblast.
 

Phenotypic Data

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Remarks Clinically affected; pancytopenia; brown patchy pigmentation on skin; untransformed fibroblasts are not sensitive to cell killing by mitomycin-C or diepoxybutane even at higher concentrations; modal number of chromosomes is 114, range is 106 to 122; structural aberrations & polyploidy; SV40 transformed GM02053.

Publications

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Ruppitsch W, Meisslitzer C, Weirich-Schwaiger H, Klocker H, Scheidereit C, Schweiger M, Hirsch-Kauffmann M, The role of oxygen metabolism for the pathological phenotype of Fanconi anemia. Hum Genet99:710-9 1997
PubMed ID: 9187662
 
Saito H, Grompe M, Neeley TL, Jakobs PM, Moses RE, Fanconi anemia cells have a normal gene structure for topoisomerase I. Hum Genet93:583-6 1994
PubMed ID: 8168839
 
Saito H, Moses RE, Immortalization of Werner syndrome and progeria fibroblasts Experimental cell research192:373-9 1991
PubMed ID: 1671011

External Links

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dbSNP dbSNP ID: 16966

Culture Protocols

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Passage Frozen 27
Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 10% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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