GM10207
LCL from B-Lymphocyte
Description:
OROFACIAL CLEFT 1; OFC1
TRANSLOCATED CHROMOSOME
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Heritable Diseases Chromosome Abnormalities |
Class |
Disorders of Connective Tissue, Muscle, and Bone |
Biopsy Source
|
Peripheral vein
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Cell Type
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B-Lymphocyte
|
Tissue Type
|
Blood
|
Transformant
|
Epstein-Barr Virus
|
Sample Source
|
LCL from B-Lymphocyte
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Race
|
White
|
Ethnicity
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GERMAN
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Relation to Proband
|
proband
|
Confirmation
|
Clinical summary/Case history
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ISCN
|
46,XY,t(10;14)(10qter>10p13::14q24.3> 14qter;14pter>14q24.3::10p13>10pter)
|
Species
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Homo sapiens
|
Common Name
|
Human
|
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 |
|
Cytogenetics |
Chromosome 10: TRANSLOCATION Breakpoint 10p13 t(10;14)10p13 |
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Chromosome 14: TRANSLOCATION Breakpoint 14q24 t(10;14)14q24 |
Remarks |
Bilateral cleft lip without cleft palate; 46,XY,t(10;14)(p13;q24.3); balanced; history of recurrent miscarriages; son with the same balanced translocation has a ventricular septal defect |
Schuffenhauer S, Lichtner P, Peykar-Derakhshandeh P, Murken J, Haas OA, Back E, Wolff G, Zabel B, Barisic I, Rauch A, Borochowitz Z, Dallapiccola B, Ross M, Meitinger T, Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2). Eur J Hum Genet6:213-25 1998 |
PubMed ID: 9781025 |
|
Cowchock S, Apparently balanced chromosome translocations and midline defects [letter] Am J Med Genet33:424 1989 |
PubMed ID: 2801781 |
Split Ratio |
1:4 |
Temperature |
37 C |
Percent CO2 |
5% |
Percent O2 |
AMBIENT |
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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