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,XX,t(11;16)(11pter>11q13::16p11> 16pter;16qter>16p11::11q13>11qter)
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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 |
8 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
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| Cytogenetics |
Chromosome 11: TRANSLOCATION Breakpoint 11q13 t(11;16)11q13 |
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Chromosome 16: TRANSLOCATION Breakpoint 16p11 t(11;16)16p11 |
| Remarks |
Phenotypically normal; mother and daughter have same balanced translocation |
| Junien C, van Heyningen V, Evans G, Little P, Mannens M, Report of the second chromosome 11 workshop. Genomics12:620-5 1992 |
| PubMed ID: 1348491 |
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| Rettig WJ, Grzeschik KH, Yenamandra AK, Garcia E, Old LJ, Definition of selectable cell surface markers for human chromosomes and chromosome segments in rodent-human hybrids. Somat Cell Mol Genet14:223-31 1988 |
| PubMed ID: 3163425 |
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| Koeffler, Regional assignment of the human genes for alpha-globin and phosphoglycolate phosphatase to 16p. Cytogenet Cell Genet32:291 (1982):223-31 1982 |
| PubMed ID: 3163425 |
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| Koeffler HP, Sparkes RS, Stang H, Mohandas T, Regional assignment of genes for human alpha-globin and phosphoglycollate phosphatase to the short arm of chromosome 16. Proc Natl Acad Sci U S A78:7015-8 1981 |
| PubMed ID: 6273902 |
| Passage Frozen |
8 |
| Split Ratio |
1:2 |
| 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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