Description:
TRANSLOCATED CHROMOSOME
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Chromosome Abnormalities |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Race
|
White
|
Relation to Proband
|
proband
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
ISCN
|
46,XX,t(11;16)(11pter>11q13::16p11> 16pter;16qter>16p11::11q13>11qter)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
8 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome 11: TRANSLOCATION Breakpoint 11q13 t(11;16)11q13 |
|
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 |
|
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 |
|
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 |
|
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 |
- |
|
|