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GM26046 Fibroblast from Skin, Arm

Description:

RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL
BRCA1-ASSOCIATED ATM ACTIVATOR 1; BRAT1

Affected:

No

Sex:

Male

Age:

34 YR (At Sampling)

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
PIGI Consented Sample
Biopsy Source Arm
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Arm
Race White
Ethnicity Not Hispanic/Latino
Ethnicity Amish
Country of Origin USA
Family Member 2
Family History Y
Relation to Proband father
Species Homo sapiens
Common Name Human
Remarks Unaffected carrier father of GM26045 (fibro); mutation in the BRAT1 gene: c.638_639insA; 2 children (1 in repository) with recessive lethal neonatal rigidity and multifocal seizure syndrome; genetic testing in 2nd child revealed a homozygous recessive mutation in the BRAT1 gene: c.638_639insA.

Characterizations

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PDL at Freeze 2.59
Passage Frozen 2
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene BRAT1
Chromosomal Location 7p22.3
Allelic Variant 1 614506.0001; RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL
Identified Mutation c.638_639insA; By homozygosity mapping followed by exome sequencing of 2 Amish patients from Pennsylvania with lethal neonatal rigidity and multifocal seizure syndrome (RMFSL; 614498), Puffenberger et al. (2012) identified a homozygous 1-bp insertion (638_639insA) in the BRAT1 gene, resulting in a frameshift and premature termination. Two unrelated Old Order Amish infants from different demes in Wisconsin and Kentucky with a similar phenotype were found to carry the same homozygous mutation. Two heterozygous carriers of this mutation were found among 201 Old Order Amish control samples, yielding a population-specific allele frequency of 0.50%. The mutation abolished the nuclear localization signal, and rendered the protein unstable when expressed in human cells as shown by Western blot analysis.

Phenotypic Data

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Remarks Unaffected carrier father of GM26045 (fibro); mutation in the BRAT1 gene: c.638_639insA; 2 children (1 in repository) with recessive lethal neonatal rigidity and multifocal seizure syndrome; genetic testing in 2nd child revealed a homozygous recessive mutation in the BRAT1 gene: c.638_639insA.

External Links

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Gene Cards BRAT1
NCBI GTR 614498 RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL
614506 BRCA1-ASSOCIATED ATM ACTIVATOR 1; BRAT1
OMIM 614498 RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL
614506 BRCA1-ASSOCIATED ATM ACTIVATOR 1; BRAT1

Culture Protocols

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Cumulative PDL at Freeze 5.89
Passage Frozen 2
Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Percent O2 3%
Medium Eagles Minimum Essential Medium with Earle's salts:Dulbecco's modified MEM with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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