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GM03808 Fibroblast

Description:

WILMS TUMOR 1; WT1
CHROMOSOME DELETION

Affected:

Yes

Sex:

Male

Age:

9 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
Chromosome Abnormalities
Class Heritable Cancer Syndromes and other Cancers
Cell Type Fibroblast
Transformant Untransformed
Race White
Relation to Proband proband
Confirmation Clinical summary/Case history
ISCN 46,XY,del(11)(pter>p14::p11.2>qter)
Species Homo sapiens
Common Name Human
Remarks AGR triad; seizures; Wilms tumor; 46,XY, del(11)(pter>p1400::p11.2>qter); lacks 1 copy of catalase gene

Characterizations

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Passage Frozen 2
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Chromosome Analysis
 
GENE MAPPING & DOSAGE STUDIES - CHROMOSOME 11 Gessler et al (Am J Hum Genet 44:486-495,1989) utilized 37 DNA probes which map to the WAGR region of chromosome 11 to define the WAGR gene loci and provide a high resolution map of this region. DNA from this cell culture showed reduced dosage, indicative of a heterozygous deletion, for at least some of the probes tested.
 
Cytogenetics Chromosome 11: DELETION Aneuploid Segment (-)11p14>11p11

Phenotypic Data

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Remarks AGR triad; seizures; Wilms tumor; 46,XY, del(11)(pter>p1400::p11.2>qter); lacks 1 copy of catalase gene

Publications

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Treff NR, Zimmerman R, Bechor E, Hsu J, Rana B, Jensen J, Li J, Samoilenko A, Mowrey W, Van Alstine J, Leondires M, Miller K, Paganetti E, Lello L, Avery S, Hsu S, Melchior Tellier LCA, Validation of concurrent preimplantation genetic testing for polygenic and monogenic disorders, structural rearrangements, and whole and segmental chromosome aneuploidy with a single universal platform European journal of medical genetics62:103647 2019
PubMed ID: 31026593
 
Gessler M, Hameister H, Henry I, Junien C, Braun T, Arnold HH, The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith- Wiedemann syndrome. Hum Genet86:135-8 1990
PubMed ID: 2176177
 
Gessler M, Thomas GH, Couillin P, Junien C, McGillivray BC, Hayden M, Jaschek G, Bruns GA, A deletion map of the WAGR region on chromosome 11. Am J Hum Genet44:486-95 1989
PubMed ID: 2539014

External Links

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dbSNP dbSNP ID: 23296
NCBI GTR 194070 WILMS TUMOR 1; WT1
OMIM 194070 WILMS TUMOR 1; WT1
Omim Description NEPHROBLASTOMA
  WILMS TUMOR 1; WT1

Culture Protocols

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Passage Frozen 2
Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
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International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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