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NA10890 DNA from Somatic cell hybrid

Description:

CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS

Affected:

No Data

Sex:

No Data

Age:

No Data

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Hybrids
Quantity 0.050mg
Quantitation Method Please see our FAQ
Cell Type Somatic cell hybrid
Transformant Untransformed
Sample Source DNA from Somatic cell hybrid
Confirmation Clinical summary/Case history
ISCN Mouse/human somatic cell hybrid retaining a human der(Y) chromosome
Remarks Line Y17-41; produced by fusing GM06326, 46,X,t(Y;17)(q11;q12), with the TK-deficient mouse cell line Cl1D; selected in HAT medium; retains the human der(Y) in 100% of cells & no other intact human chromosomes

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 and by Chromosome Analysis
 
GENE MAPPING & DOSAGE STUDIES - Y CHROMOSOME DNA from this somatic cell hybrid gave a negative result in Southern blot hybridization analysis with a probe for Yq12, DYZ1, and gave a positive result with a probe for Yp11.3 and Xp22.32, DXYS20.
 
GENE MAPPING & DOSAGE STUDIES - CHROMOSOME 17 DNA from this somatic cell hybrid gave a negative result in Southern blot hybridization analysis with a probe for 17p13.1, MYH2, and gave a positive result with a probe for 17q21.3q23, MPO.
 

Phenotypic Data

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Remarks Line Y17-41; produced by fusing GM06326, 46,X,t(Y;17)(q11;q12), with the TK-deficient mouse cell line Cl1D; selected in HAT medium; retains the human der(Y) in 100% of cells & no other intact human chromosomes

Publications

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Penin J, Dufour S, Faure V, Fritah S, Seigneurin-Berny D, Col E, Verdel A, Vourc'h C, Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells Chromosoma130:53-60 2020
PubMed ID: 33547955
 
Plummer SJ, Simmons JA, Adams L, Casey G, Mapping of 228 ESTs and 26 genes into an integrated physical and genetic map of human chromosome 17. Genomics45:140-6 1997
PubMed ID: 9339370
 
Verdier AS, Mattei MG, Lovec H, Hartung H, Goldfarb M, Birnbaum D, Coulier F, Chromosomal mapping of two novel human FGF genes, FGF11 and FGF12. Genomics40:151-4 1997
PubMed ID: 9070933
 
Bukvic N, Susca F, Gentile M, Tangari E, Ianniruberto A, Guanti G, An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite. Hum Genet97:453-6 1996
PubMed ID: 8834241
 
Kusuda J, Hidari N, Hirai M, Hashimoto K, Sequence analysis of the cDNA for the human casein kinase I delta (CSNK1D) gene and its chromosomal localization. Genomics32:140-3 1996
PubMed ID: 8786104
 
Kusuda J, Tanuma R, Gotoh E, Toyoda A, Hashimoto K, Assignment of a human autoimmune antigen, p80-coilin gene to chromosome 17q21-q23 and of its possible pseudogene to chromosome 14. Hum Genet95:233-4 1995
PubMed ID: 7860074
 
Polymeropoulos MH, Torres R, Yanovski JA, Chandrasekharappa SC, Ledbetter DH, The human corticotropin-releasing factor receptor (CRHR) gene maps to chromosome 17q12-q22. Genomics28:123-4 1995
PubMed ID: 7590738

External Links

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dbSNP dbSNP ID: 11444
Pricing
International/Commercial/For-profit:
$449.00USD
U.S. Academic/Non-profit/Government:
$263.00USD
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