GM13166
LCL from B-Lymphocyte
Description:
TURNER SYNDROME
ISOCHROMOSOME
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Chromosome Abnormalities dbGaP |
Biopsy Source
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Peripheral vein
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Cell Type
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B-Lymphocyte
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Tissue Type
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Blood
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Transformant
|
Epstein-Barr Virus
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Sample Source
|
LCL from B-Lymphocyte
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Relation to Proband
|
proband
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Confirmation
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Clinical summary/Case history
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ISCN
|
46,X,idic(X)(p11.2)[35]/45,X[15].arr Xp22.33p11.21(109804-55438185)x1,Xp11.21q28(55583648-154887040)x3
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Species
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Homo sapiens
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Common Name
|
Human
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Remarks
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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 |
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Cytogenetics |
Chromosome X: ISOCHROMOSOME Aneuploid Segment (+)Xqter>Xq10 |
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Chromosome X: ISOCHROMOSOME Aneuploid Segment (-)Xpter>Xp10 |
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Chromosome X: ISOCHROMOSOME Trisomic Segment Xqter>Xq10 |
Remarks |
Turner syndrome; short stature and primary amenorrhea; 30% of cells are 45,X |
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 |
PubMed ID: 23665875 |
Split Ratio |
1:3 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not Inactivated |
Substrate |
None specified |
Subcultivation Method |
dilution - add fresh medium |
Supplement |
- |
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