GM04627
Amniotic fluid-derived cell line from Amniotic fluid
Description:
RECOMBINANT CHROMOSOME
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Chromosome Abnormalities |
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Biopsy Source
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Amniotic fluid
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Cell Type
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Amniotic fluid-derived cell line
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Transformant
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Untransformed
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Sample Source
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Amniotic fluid-derived cell line from Amniotic fluid
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Race
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White
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Family Member
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2
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Relation to Proband
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brother
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Confirmation
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Karyotypic analysis after cell line submission to CCR
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ISCN
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46,XY,rec(3)(qter>p25::q21>qter), 9qh+
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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| Passage Frozen |
5 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
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| Remarks |
Mother has inv(3)(p25q21); 46,XY,rec(3), dup q,inv(3)(qter>p25::q21>qter), 9qh+; unbalanced; brother is GM00366 Fibroblast |
| Allderdice PW, Browne N, Murphy DP, Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21). Am J Hum Genet27:699-718 1975 |
| PubMed ID: 1200027 |
| Passage Frozen |
5 |
| 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 |
- |
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