NA13325
DNA from Fibroblast
Description:
DIGEORGE SYNDROME; DGS
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases dbGaP |
Class |
Other Disorders of Known Biochemistry |
Quantity |
0.050mg |
Quantitation Method |
Please see our FAQ |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Sample Source
|
DNA from Fibroblast
|
Race
|
White
|
Country of Origin
|
USA
|
Family Member
|
1
|
Relation to Proband
|
proband
|
Confirmation
|
Molecular characterization after cell line submission to CCR
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
PDL at Freeze |
2.19 |
Passage Frozen |
2 |
|
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 22: DELETION Aneuploid Segment (-)22q11>22q11 |
Remarks |
Clinically affected; del(22)(q11) confirmed by FISH analysis with a cosmid probe to the DiGeorge syndrome critical region. |
Goh CJ, Kwon HJ, Kim Y, Jung S, Park J, Lee IK, Park BR, Kim MJ, Kim MJ, Lee MS, Improving CNV Detection Performance in Microarray Data Using a Machine Learning-Based Approach Diagnostics (Basel, Switzerland)14: 2023 |
PubMed ID: 38201393 |
|
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 |
dbSNP |
dbSNP ID: 11766 |
NCBI Gene |
Gene ID:1714 |
NCBI GTR |
188400 DIGEORGE SYNDROME; DGS |
OMIM |
188400 DIGEORGE SYNDROME; DGS |
Omim Description |
CATCH22, INCLUDED |
|
CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED |
|
DIGEORGE SYNDROME; DGS |
|
HYPOPLASIA OF THYMUS AND PARATHYROIDS |
|
SHPRINTZEN VCF SYNDROME, INCLUDED |
|
TAKAO VCF SYNDROME, INCLUDED |
|
THIRD AND FOURTH PHARYNGEAL POUCH SYNDROMEDIGEORGE SYNDROME CHROMOSOME REGION, INCLUDED; DGCR, INCLUDED |
|
VELOCARDIOFACIAL SYNDROME, INCLUDED |
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