NA00271
DNA from Fibroblast
Description:
TRANSLOCATED CHROMOSOME
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Chromosome Abnormalities |
Quantity |
10 µg |
Quantitation Method |
Please see our FAQ |
Cell Type
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Fibroblast
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Transformant
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Untransformed
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Sample Source
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DNA from Fibroblast
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Race
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White
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Relation to Proband
|
parent
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Confirmation
|
Karyotypic analysis after cell line submission to CCR
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ISCN
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46,XX,t(17;19)(17pter>17q23::19p13> 19pter;19qter>19p13::17q23>17qter)
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
|
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Passage Frozen |
3 |
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IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
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Cytogenetics |
Chromosome 17: TRANSLOCATION Breakpoint 17q23 t(17;19)17q23 |
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Chromosome 19: TRANSLOCATION Breakpoint 19p13 t(17;19)19p13 |
Remarks |
Normal phenotype; 1 spontaneous abortion and 1 stillborn with anomalies |
van Tuinen P, Rich DC, Summers KM, Ledbetter DH, Regional mapping panel for human chromosome 17: application to neurofibromatosis type 1. Genomics1:374-81 1987 |
PubMed ID: 3130306 |
|
Chen SH, Van Tuinen P, Ledbetter DH, Smith LC, Chan L, Human liver fatty acid binding protein gene is located on chromosome 2. Somat Cell Mol Genet12:303-6 1986 |
PubMed ID: 3012800 |
|
Kim HJ, Hsu LY, Hirschhorn K, Miller RC, Greene AE, Coriell LL, A (17;19) translocation, balanced, 46 chromosomes. Repository identification No. GM-271. Cytogenet Cell Genet14:92-3 1975 |
PubMed ID: 1169138 |
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