Description:
TRANSLOCATED CHROMOSOME
|
Repository
|
NIGMS Human Genetic Cell Repository
|
| Subcollection |
Chromosome Abnormalities dbGaP |
|
Cell Type
|
Fibroblast
|
|
Transformant
|
Untransformed
|
|
Race
|
White
|
|
Ethnicity
|
PORTUGUESE
|
|
Relation to Proband
|
proband
|
|
Confirmation
|
Clinical summary/Case history
|
|
ISCN
|
46,X,der(X)(Xpter>Xq28::2p21>2pter)mat
|
|
Species
|
Homo sapiens
|
|
Common Name
|
Human
|
|
Remarks
|
|
| Passage Frozen |
17 |
| |
| 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 2: DERIVATIVE CHROMOSOME Aneuploid Segment (+)2pter>2p21 |
|
Chromosome 2: DERIVATIVE CHROMOSOME Trisomic Segment 2pter>2p21 |
|
Chromosome X: DERIVATIVE CHROMOSOME Aneuploid Segment (-)Xq28>Xqter |
| Remarks |
Congenital heart disease; growth and mental retardation; alacrima; unusual triangular facies; strabismus; frontal bossing; simple, low set, posteriorly rotated ears; hypotonia |
| Walters-Sen L, Neitzel D, Bristow SL, Mitchell A, Alouf CA, Aradhya S, Faulkner N, Experience analysing over 190,000 embryo trophectoderm biopsies using a novel FAST-SeqS preimplantation genetic testing assay Reproductive biomedicine online44:228-238 2022 |
| PubMed ID: 35039224 |
| |
| 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 |
| |
| Taylor Clelland CL, Levy B, McKie JM, Duncan AM, Hirschhorn K, Bancroft C, Cloning and characterization of human PREB; a gene that maps to a genomic region
associated with trisomy 2p syndrome. Mamm Genome11(8):675-81 2000 |
| PubMed ID: 10920239 |
| |
| Leach FS, Nicolaides NC, Papadopoulos N, Liu B, Jen J, Parsons R, Peltomaki P, Sistonen P, Aaltonen LA, Nystrom-Lahti M, et al, Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell75:1215-25 1993 |
| PubMed ID: 8261515 |
| |
| Scola, 2p partial trisomy. Am J Hum Genet31:110A (1979):1215-25 1979 |
| PubMed ID: 8261515 |
| Passage Frozen |
17 |
| 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 |
- |
|
|