Description:
TRANSLOCATED CHROMOSOME
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Chromosome Abnormalities |
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Cell Type
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Fibroblast
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Transformant
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Untransformed
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Race
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White
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Relation to Proband
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proband
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Confirmation
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Karyotypic analysis after cell line submission to CCR
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ISCN
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46,XY,t(9;13)(9qter>9p22 or p23::13q14 or q21>13qter;13pter>13q14 or q21::9p22 or p23>9pter)
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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 |
6 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
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| Cytogenetics |
Chromosome 13: TRANSLOCATION Breakpoint 13q14 t(9;13)13q14 |
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Chromosome 13: TRANSLOCATION Breakpoint 13q21 t(9;13)13q21 |
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Chromosome 9: TRANSLOCATION Breakpoint 9p22 t(9;13)9p22 |
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Chromosome 9: TRANSLOCATION Breakpoint 9p23 t(9;13)9p23 |
| Remarks |
Phenotypically normal; family history of recurrent abortions |
| Serra A, Ricci R, Aronson MM, Mulivor RA, Greene AE, Coriell LL, A familial t(9;13) balanced translocation associated with recurrent abortion. Repository identification No. GM2492. Cytogenet Cell Genet27:269 1980 |
| PubMed ID: 7438787 |
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| Singh-Kahlon D, Serra A, Familial C/D translocation t(9;13)(9p23.13q21) in a male associated with recurrent abortion. Hum Genet33:223-30 1976 |
| PubMed ID: 964984 |
| Passage Frozen |
6 |
| Split Ratio |
1:3 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
| Serum |
15% fetal bovine serum Not inactivated |
| Substrate |
None specified |
| Subcultivation Method |
trypsin-EDTA |
| Supplement |
- |
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