Description:
TRANSLOCATED CHROMOSOME
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Chromosome Abnormalities |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Race
|
White
|
Family Member
|
2
|
Relation to Proband
|
mother
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
ISCN
|
46,XX,t(8;15)(8qter>8p21::15q26>15qter; 15pter>15q26::8p21>8pter)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
3 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome 15: TRANSLOCATION Breakpoint 15q26 t(8;15)15q26 |
|
Chromosome 8: TRANSLOCATION Breakpoint 8p21 t(8;15)8p21 |
Remarks |
Clinically normal |
Lin MS, Zhang A, Fujimoto A, Asynchronous DNA replication between 15q11.2q12 homologs: cytogenetic evidence for maternal imprinting and delayed replication. Hum Genet96(5):572-6 1995 |
PubMed ID: 8530005 |
|
Jones LA, Dengler DR, Taysi K, Shackelford GD, Hartmann AF, Partial trisomy of the short arm of chromosome 8 resulting from balanced maternal translocation. J Med Genet17:232-5 1980 |
PubMed ID: 7401137 |
Passage Frozen |
3 |
Split Ratio |
1:5 |
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 |
- |
|
|