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GM24467 Fibroblast from Skin, Skin

Description:

SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
SELENOPROTEIN N, 1; SEPN1

Affected:

Yes

Sex:

Female

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
Class Congenital Muscle Diseases
Biopsy Source Skin
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Skin
Race White
Ethnicity Not Hispanic/Latino
Country of Origin USA
Family History N
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected; motor functions achieved: turned in bed at 6 months, sat without assistance at 6 months, stood without assistance at 12 months, walked at 14 months, climbed stairs at 18 months, ran at 16 months; constipation; alveolar hypoventilation requiring bipap and cough assist; rigid spine with scoliosis in the lumbar region; Northstar Assessment Score of 29 out of 34; CK: 125; respiratory status: FVC (liters) 0.8 liters, FVC% predicted 55, MIP:35, MIP%59, MEP 39, MEP% 60, cough peak flow: 120; donor subject is heterozygous for a mutation (c.142delG) in exon 1 of the SEPN1 gene predicting premature protein termination (p.Val48SerfsStop18); donor subject is also heterozygous for a mutation (c.943G>A) in exon 7 of the SEPN1 gene predicting a p.Gly315Ser amino acid substitution; medications include Miralax; wears glasses and TSLO brace; surgeries include: g-tube placement for food aversion and failure to thrive.

Characterizations

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PDL at Freeze 3.23
Passage Frozen 2
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene SEPN1
Chromosomal Location 1p36-p35
Allelic Variant 1 606210.0008;
Identified Mutation c.943G>A
 
Gene SEPN1
Chromosomal Location 1p36-p35
Allelic Variant 1 Frameshift;
Identified Mutation c.142delG

Phenotypic Data

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Remarks Clinically affected; motor functions achieved: turned in bed at 6 months, sat without assistance at 6 months, stood without assistance at 12 months, walked at 14 months, climbed stairs at 18 months, ran at 16 months; constipation; alveolar hypoventilation requiring bipap and cough assist; rigid spine with scoliosis in the lumbar region; Northstar Assessment Score of 29 out of 34; CK: 125; respiratory status: FVC (liters) 0.8 liters, FVC% predicted 55, MIP:35, MIP%59, MEP 39, MEP% 60, cough peak flow: 120; donor subject is heterozygous for a mutation (c.142delG) in exon 1 of the SEPN1 gene predicting premature protein termination (p.Val48SerfsStop18); donor subject is also heterozygous for a mutation (c.943G>A) in exon 7 of the SEPN1 gene predicting a p.Gly315Ser amino acid substitution; medications include Miralax; wears glasses and TSLO brace; surgeries include: g-tube placement for food aversion and failure to thrive.

External Links

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Gene Cards SELENON
SEPN1
Gene Ontology GO:0000004 biological_process unknown
GO:0005509 calcium ion binding
GO:0005576 extracellular
GO:0005783 endoplasmic reticulum
NCBI Gene Gene ID:57190
NCBI GTR 602771 SELENON-RELATED MYOPATHY RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
606210 SELENOPROTEIN N; SELENON
OMIM 602771 SELENON-RELATED MYOPATHY RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
606210 SELENOPROTEIN N; SELENON
Omim Description MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE, WITH EARLY SPINERIGIDITY

Culture Protocols

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Cumulative PDL at Freeze 3.23
Passage Frozen 2
Split Ratio 1:7
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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