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,XY,der(1)(1pter>1q32::3p21>3pter),der(3)(1qter>1q32::3p21>3q29::4p14>4pter),der(4)(4qter>4p14::3q29>3qter)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
6 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome 1: TRANSLOCATION Breakpoint 1q32 t(1;3;4)1q32 |
|
Chromosome 3: TRANSLOCATION Breakpoint 3p21 t(1;3;4)3p21 |
|
Chromosome 3: TRANSLOCATION Breakpoint 3q29 t(1;3;4)3q29 |
|
Chromosome 4: TRANSLOCATION Breakpoint 4p14 t(1;3;4)4p14 |
Remarks |
Family history of multiple abortions; wife is 46,XX |
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 |
- |
|
|