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GM13325 Fibroblast

Description:

DIGEORGE SYNDROME; DGS

Affected:

Yes

Sex:

Female

Age:

9 DA (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
dbGaP
Class Other Disorders of Known Biochemistry
Cell Type Fibroblast
Transformant Untransformed
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 Clinically affected; del(22)(q11) confirmed by FISH analysis with a cosmid probe to the DiGeorge syndrome critical region.

Characterizations

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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

Phenotypic Data

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Remarks Clinically affected; del(22)(q11) confirmed by FISH analysis with a cosmid probe to the DiGeorge syndrome critical region.

Publications

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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

External Links

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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

Images

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View copy number variation 
copy number variation 

Culture Protocols

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Cumulative PDL at Freeze 5.97
Passage Frozen 2
Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium MEM (Eagle) Alpha Modification with nucleosides with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Heat Inactivated
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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How to Order
  • Ordering Instructions
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