Description:
TRANSLOCATED CHROMOSOME
Repository
|
NIGMS Human Genetic Cell Repository
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Subcollection |
Chromosome Abnormalities |
Quantity |
25 µg |
Quantitation Method |
Please see our FAQ |
Biopsy Source
|
Peripheral vein
|
Cell Type
|
B-Lymphocyte
|
Tissue Type
|
Blood
|
Transformant
|
Epstein-Barr Virus
|
Sample Source
|
DNA from LCL
|
Race
|
White
|
Family Member
|
1
|
Relation to Proband
|
mother
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
ISCN
|
46,XX,t(10;21)(10qter>10p11.2::21q22.3> 21qter;21pter>21q22.3::10p11.2>10pter)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome 10: TRANSLOCATION Breakpoint 10p11 t(10;21)10p11 |
|
Chromosome 21: TRANSLOCATION Breakpoint 21q22 t(10;21)21q22 |
Remarks |
Clinically normal |
Ye MH, Saito-Ohara F, Ikeuchi T, High-resolution chromosome R-banding in lymphoblastoid cell lines by the combined use of cell synchronization and ethidium bromide treatment. Jpn J Hum Genet41:203-8 1996 |
PubMed ID: 8914636 |
|
Jenkins EC, Devine-Gage EA, Robakis NK, Yao XL, Brown WT, Houck GE Jr, Wolfe G, Ramakrishna N, Silverman WP, Wisniewski HM, Fine mapping of an Alzheimer disease-associated gene encoding beta-amyloid protein. Biochem Biophys Res Commun151:1-8 1988 |
PubMed ID: 3279948 |
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