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GM26093 Fibroblast from Skin, Hip

Description:

NEMALINE MYOPATHY 2, AUTOSOMAL RECESSIVE; NEM2
NEBULIN; NEB

Affected:

Yes

Sex:

Male

Age:

6 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
Muscular Dystrophies
CMD Specific
PIGI Consented Sample
Biopsy Source Hip
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Hip
Race More than one race
Ethnicity Not Hispanic/Latino
Ethnicity Chinese/Ashkenazi Jewish
Country of Origin USA
Family Member 1
Family History N
Relation to Proband proband
Confirmation Clinical summary/Case history
ISCN 46,XY[20]
Species Homo sapiens
Common Name Human
Remarks Clinically affected; symptom onset at birth; achieved/maintained motor functions: held head up without assistance, turned in bed without assistance at age 6 months, sat without assistance at age 8 months, stood without assistance at age 1.5 years, walked with assistance at age 2 years, walked indoors and outdoors unassisted at age 2 years old; gene sequencing of TPM3,TPM2 and NEB genes identified heterozygous mutation defined as c.9619-2A>G near the junction of intron 66 and exon 67 of the NEB gene; subject is also heterozygous for mutation defined as c.24473_24476dupAACA which is predicted to result in a frame shift and premature protein termination (p.His8159GlnfsStop8); respiratory support used during perinatal period; lymphoblast is GM25172.

Characterizations

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PDL at Freeze 6.35
Passage Frozen 2
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene NEB
Chromosomal Location 2q23.3
Allelic Variant 1 ; NEMALINE MYOPATHY 2 (NEM2)
Identified Mutation c.9619-2A>G
 
Gene NEB
Chromosomal Location 2q23.3
Allelic Variant 1 p.His8159GlnfsStop8; NEMALINE MYOPATHY 2 (NEM2)
Identified Mutation c.24473_24476dupAACA

Phenotypic Data

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Remarks Clinically affected; symptom onset at birth; achieved/maintained motor functions: held head up without assistance, turned in bed without assistance at age 6 months, sat without assistance at age 8 months, stood without assistance at age 1.5 years, walked with assistance at age 2 years, walked indoors and outdoors unassisted at age 2 years old; gene sequencing of TPM3,TPM2 and NEB genes identified heterozygous mutation defined as c.9619-2A>G near the junction of intron 66 and exon 67 of the NEB gene; subject is also heterozygous for mutation defined as c.24473_24476dupAACA which is predicted to result in a frame shift and premature protein termination (p.His8159GlnfsStop8); respiratory support used during perinatal period; lymphoblast is GM25172.

External Links

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Gene Cards NEB
Gene Ontology GO:0003779 actin binding
GO:0007525 somatic muscle development
GO:0008307 structural constituent of muscle
GO:0015629 actin cytoskeleton
GO:0030017 sarcomere
GO:0030832 regulation of actin filament length
NCBI Gene Gene ID:4703
NCBI GTR 161650 NEBULIN; NEB
256030 NEMALINE MYOPATHY 2; NEM2
OMIM 161650 NEBULIN; NEB
256030 NEMALINE MYOPATHY 2; NEM2
Omim Description NEMALINE MYOPATHY 2, AUTOSOMAL RECESSIVE; NEM2

Culture Protocols

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Cumulative PDL at Freeze 6.35
Passage Frozen 2
Split Ratio 1:7
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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