Description:
XXY SYNDROME; KLINEFELTER SYNDROME
ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Chromosome Abnormalities dbGaP |
Cell Type
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Fibroblast
|
Transformant
|
Untransformed
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Race
|
White
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Relation to Proband
|
proband
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
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ISCN
|
48,XXYY.arr(X)x2,Yp11.31p11.223(2710425-23302179)x2,Yq11.23q12(26868023-27209311)x2
|
Species
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Homo sapiens
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Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
4 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome X: ANEUPLOID Aneuploid Segment (+)Xpter>Xqter |
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Chromosome Y: ANEUPLOID Aneuploid Segment (+)Ypter>Yqter |
Remarks |
Klinefelter's syndrome variant |
Chien CW, Tang YA, Jeng SL, Pan HA, Sun HS, Blastocyst telomere length predicts successful implantation after frozen-thawed embryo transfer Human reproduction open2024:hoae012 2023 |
PubMed ID: 38515829 |
|
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 |
PubMed ID: 23665875 |
|
Ballif BC, Kashork CD, Saleki R, Rorem E, Sundin K, Bejjani BA, Shaffer LG, Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization Prenatal diagnosis26:333-9 2006 |
PubMed ID: 16491513 |
|
Mutter GL, Pomponio RJ, Molecular diagnosis of sex chromosome aneuploidy using quantitative PCR. Nucleic Acids Res19:4203-7 1991 |
PubMed ID: 1678507 |
Passage Frozen |
4 |
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 |
- |
|
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