GM11239
Amniotic fluid-derived cell line from Amniotic fluid
Description:
TRANSLOCATED CHROMOSOME
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Chromosome Abnormalities |
Biopsy Source
|
Amniotic fluid
|
Cell Type
|
Amniotic fluid-derived cell line
|
Transformant
|
Untransformed
|
Sample Source
|
Amniotic fluid-derived cell line from Amniotic fluid
|
Race
|
White
|
Relation to Proband
|
proband
|
Confirmation
|
Clinical summary/Case history
|
ISCN
|
46,XX,t(1:16)(1pter>1q24::16q21>16qter; 16pter>16q21::1q24>1qter)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
3 |
|
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 1: TRANSLOCATION Breakpoint 1q24 t(1:16)1q24 |
|
Chromosome 16: TRANSLOCATION Breakpoint 16q21 t(1:16)16q21 |
Remarks |
46,XX,t(1;16)(1pter>1q24::16q21>16qter; 16pter>16q21::1q24>1qter); balanced; de novo translocation |
Passage Frozen |
3 |
Split Ratio |
1:5 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Amniotic Fluid Culture Medium |
Serum |
none Not inactivated |
Substrate |
None specified |
Subcultivation Method |
trypsin-EDTA |
Supplement |
- |
|
|