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GM22766 LCL from B-Lymphocyte

Description:

SMITH-MAGENIS SYNDROME; SMS
RETINOIC ACID-INDUCED GENE 1; RAI1

Affected:

Yes

Sex:

Female

Age:

7 YR (At Sampling)

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Chromosome Abnormalities
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race East Indian
Ethnicity PAKISTANI/AFGHANI/PERSIAN/PORTUGUESE/GERMAN
Family Member 1
Family History N
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
ISCN 46,XX.ish 17p11.2(LIS1,FLI1)x2
Species Homo sapiens
Common Name Human
Remarks Clinically affected; low set angular ears; upslanting eyes; hypertelorism seizures; frequent ear and respiratory infections; constipation; speech delay; intellectual disability; sleep disturbance; repetitive behaviors; delayed toilet training; donor subject has a G>T change at nucleotide 223 of the RAI1 gene resulting in the substitution of serine for alanine at codon 75 [Ala75Ser (A75S)]; mother is GM22767.

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin confirmed by LINE assay
 
Gene RAI1
Chromosomal Location 17p11.2
Allelic Variant 1 A75S; SMITH-MAGENIS SYNDROME
Identified Mutation ALA75SER

Phenotypic Data

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Remarks Clinically affected; low set angular ears; upslanting eyes; hypertelorism seizures; frequent ear and respiratory infections; constipation; speech delay; intellectual disability; sleep disturbance; repetitive behaviors; delayed toilet training; donor subject has a G>T change at nucleotide 223 of the RAI1 gene resulting in the substitution of serine for alanine at codon 75 [Ala75Ser (A75S)]; mother is GM22767.

Publications

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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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Gene Cards RAI
RAI1
Gene Ontology GO:0003677 DNA binding
GO:0006355 regulation of transcription, DNA-dependent
NCBI Gene Gene ID:10743
NCBI GTR 182290 SMITH-MAGENIS SYNDROME; SMS
607642 RETINOIC ACID-INDUCED GENE 1; RAI1
OMIM 182290 SMITH-MAGENIS SYNDROME; SMS
607642 RETINOIC ACID-INDUCED GENE 1; RAI1
Omim Description SMITH-MAGENIS CHROMOSOME REGION; SMCR
  SMITH-MAGENIS SYNDROME; SMS

Images

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View FISH Texas Red detects LIS1(17p13.3), FITC detects (FLI1),DAPI counterstain
FISH Texas Red detects LIS1(17p13.3), FITC detects (FLI1),DAPI counterstain

Culture Protocols

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Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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