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GM25981 Fibroblast

Description:

MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34; MRT34

Affected:

No

Sex:

Female

Age:

43 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
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Race White
Ethnicity Not Hispanic/Latino
Ethnicity Old Order Mennonite
Country of Origin USA
Family Member 2
Family History Y
Relation to Proband mother
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Unaffected carrier; whole exome sequencing revealed a heterozygous mutation c.382G>C (p.Gly128Arg) in the CRADD gene; affected daughter is GM25980; has second affected daughter (not in catalog).

Characterizations

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PDL at Freeze 8.14
Passage Frozen 3
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene CRADD
Chromosomal Location 12q22
Allelic Variant 1 603454.p.Gly128Ar; MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34
Identified Mutation c.382G>C; In 5 Mennonite patients with autosomal recessive nonsyndromic mental retardation-34 (MRT34; 614499), Puffenberger et al. (2012) identified a homozygous 382G-C transversion in the CRADD gene, resulting in a gly128-to-arg (G128R) substitution in a highly conserved residue in the CRADD death domain. The mutation was found by homozygosity mapping followed by exome sequencing. Seven heterozygous carriers of this mutation were found among 203 Mennonite control samples, yielding a population-specific allele frequency of 1.72%. (Puffenberger (2012) stated that the correct population-specific allele frequency data appear in Table 4; corresponding data in the text are incorrect.) Overexpression of mutant murine Cradd with the G128R mutation showed normal protein localization to the nucleus and cytoplasm. However, when co-overexpressed with wildtype Pidd (605247), mutant G128R Cradd formed large cytoplasmic aggregates with a relative loss of Cradd expression in the nucleus. The findings suggested that the G128R mutation alters 1 of the interaction surfaces of the CRADD death domain to decrease affinity for the PIDD death domain.

Phenotypic Data

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Remarks Unaffected carrier; whole exome sequencing revealed a heterozygous mutation c.382G>C (p.Gly128Arg) in the CRADD gene; affected daughter is GM25980; has second affected daughter (not in catalog).

External Links

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NCBI GTR 614499 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34
OMIM 614499 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34

Culture Protocols

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Cumulative PDL at Freeze 8.14
Passage Frozen 3
Split Ratio 1:6
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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