Description:
ISOCHROMOSOME
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,i(13)(qter>q10::q10>qter)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome 13: ISOCHROMOSOME Aneuploid Segment (+)13q10>13qter |
|
Chromosome 13: ISOCHROMOSOME Aneuploid Segment (-)13p10>13pter |
|
Chromosome 13: ISOCHROMOSOME Trisomic Segment 13q10>13qter |
Remarks |
Cleft lip & palate; empty right eye socket; radial denervation of wrists; duplication of great toes; scalp hemangioma; passage 3 at IMR; 46,XX,r(13) was also seen in blood lymphocytes |
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 |
- |
|
|