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GM03197 LCL from B-Lymphocyte

Description:

TRANSLOCATED CHROMOSOME

Affected:

No Data

Sex:

Female

Age:

31 YR (At Sampling)

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Chromosome Abnormalities
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Family Member 1
Relation to Proband proband
Confirmation Karyotypic analysis after cell line submission to CCR
ISCN 46,XX,inv(5)(pter>p13::q13>p13:: q13>qter),t(17;22)(17qter>17p13:: 22q11>22qter;22pter>22q11::17p13>17pter)
Species Homo sapiens
Common Name Human
Remarks No hematological disorder; habitual aborter; normal phenotype; see GM03196 Fibroblast

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Chromosome Analysis
 
Cytogenetics Chromosome 17: TRANSLOCATION Breakpoint 17p13 t(17;22)17p13
Chromosome 22: TRANSLOCATION Breakpoint 22q11 t(17;22)22q11
Chromosome 5: INVERSION Breakpoint 5p13 inv(5)5p13
Chromosome 5: INVERSION Breakpoint 5q13 inv(5)5q13

Phenotypic Data

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Remarks No hematological disorder; habitual aborter; normal phenotype; see GM03196 Fibroblast

Publications

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Spiteri E, Babcock M, Kashork CD, Wakui K, Gogineni S, Lewis DA, Williams KM, Minoshima S, Sasaki T, Shimizu N, Potocki L, Pulijaal V, Shanske A, Shaffer LG, Morrow BE, Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes. Hum Mol Genet12(15):1823-37 2003
PubMed ID: 12874103
 
Kanda N, Fukushige S, Murotsu T, Yoshida MC, Tsuchiya M, Asano S, Kaziro Y, Nagata S, Human gene coding for granulocyte-colony stimulating factor is assigned to the q21-q22 region of chromosome 17. Somat Cell Mol Genet13:679-84 1987
PubMed ID: 3499671
 
Fukushige S, Matsubara K, Yoshida M, Sasaki M, Suzuki T, Semba K, Toyoshima K, Yamamoto T, Localization of a novel v-erbB-related gene, c-erbB-2, on human chromosome 17 and its amplification in a gastric cancer cell line. Mol Cell Biol6:955-8 1986
PubMed ID: 2430175
 
Fukushige S, Murotsu T, Matsubara K, Chromosomal assignment of human genes for gastrin, thyrotropin (TSH)- beta subunit and C-erbB-2 by chromosome sorting combined with velocity sedimentation and Southern hybridization. Biochem Biophys Res Commun134:477-83 1986
PubMed ID: 3511905
 
McBride OW, Merry D, Givol D, The gene for human p53 cellular tumor antigen is located on chromosome 17 short arm (17p13). Proc Natl Acad Sci U S A83:130-4 1986
PubMed ID: 3001719
 
Krumlauf R, Jeanpierre M, Young BD, Construction and characterization of genomic libraries from specific human chromosomes. Proc Natl Acad Sci U S A79:2971-5 1982
PubMed ID: 6953442

External Links

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dbSNP dbSNP ID: 16774

Culture Protocols

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Split Ratio 1:5
Temperature 37 C
Percent CO2 5%
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 20% 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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