Coriell Institute for Medical Research
Coriell Institute of Medical Research
  • Request a Quote
  • Donate
  • Login
  • View Cart
Sample Catalog | Custom Services | Core Facilities | Genomic Data Search
  • Biobank
    • NIGMS
    • NINDS
    • NIA
    • NHGRI
    • NEI
    • Allen Cell Collection
    • Rett Syndrome iPSC Collection
    • Autism Research Resource
    • HD Community Biorepository
    • CDC Cell and DNA
    • J. Craig Venter Institute
    • Orphan Disease Center Collection
    • All Biobanks
  • Research
    • Overview
    • Meet Our Scientists
      • Our Faculty
      • Our Scientific Staff
    • Camden Cancer Research Center
    • Epigenetic Therapies SPORE
    • Core Facilities
    • Epigenomics
    • Camden Opioid Research Initiative (CORI)
    • The Issa & Jelinek Lab
    • The Jian Huang Lab
    • The Luke Chen Lab
      • The Lab
      • The Team
      • Publications
    • The Scheinfeldt Lab
    • The Shumei Song Lab
    • The Nora Engel Lab
      • The Lab
      • The Team
      • Publications
    • Publications
  • Services
    • Overview
    • Biobanking Services
      • Core Services
      • Project Management
      • Research Support Services
      • Sample Cataloging
      • Sample Collection Kits
      • Sample Data Management
      • Sample Distribution
      • Sample Management
      • Sample Procurement
      • Sample Storage
    • Bioinformatics and Biostatistics Services
    • Cellular and Molecular Services
      • Biomarker Research Solutions
      • Cell Culture
      • Nucleic Acid Isolation and Quality Control
    • Clinical Trial Support
      • Overview
      • Sample Collection
      • Data Management
      • Sample Processing and QC
      • Storage and Distribution
      • Biomarker Services
      • Data Analaysis
    • Core Facilties
      • Overview
      • Animal and Xenograft
      • Bioinformatics and Biostatistics
      • Cell Imaging
      • CRISPR Gene Engineering
      • Flow Cytometry and Cell Sorting
      • Genomics and Epigenomics
      • iPSC - Induced Pluripotent Stem Cells
      • Organoids
    • Coriell Marketplace
    • Genomic, Epigenomic and Multiomics Services
    • Stem Cells and iPSC Services
      • Core Services
      • Reprogramming
      • Characterization and Quality Control
      • Differentiated Cell Lines
      • iPSC-Derived Organoids
      • iPSC Expansion
      • iPSC Gene Editing
  • Ordering
    • Stem Cells
    • Cell Lines
    • DNA and RNA
    • Featured Products
      • FFPE
      • HMW DNA
    • Genomic Data Search
    • Search by Catalog ID
    • Help
      • Create Account
      • Order Online
      • Ordering FAQ
      • FAQs/Culture Instructions
      • Reference Materials
        • Biobanks
        • NIGMS Repository
        • NHGRI Repository
        • NINDS Repository
        • NIA Repository
        • NIST
        • GeT-RM
      • Secondary Distribution Policies
      • MTA Assurance Form
      • Shipment Policy
      • Contact Customer Service
  • About Us
    • Our History
    • Meet Our Team
    • Meet Our Board
    • Education
      • Science Fair
      • Summer Experience
      • Outreach
      • Research Program Internship
    • Press Room
      • Press Releases
      • Coriell Blog
      • Annual Report
    • Careers
      • Working at Coriell
    • Giving
      • Donate
      • Giving FAQ
    • Contact Us
    • Legal Notice
  • Login View Cart
search submit
GM26579 Fibroblast from Skin, Flank

Description:

MYOPATHY, MYOFIBRILLAR, 13, WITH RIMMED VACUOLES; MFM13
HEAT-SHOCK 22-KD PROTEIN 8; HSPB8
RIMMED VACUOLAR MYOPATHY

Affected:

Yes

Sex:

Male

Age:

66 YR (At Sampling)

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

Overview

back to top
Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
PIGI Consented Sample
Biopsy Source Flank
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Flank
Race White
Ethnicity Not Hispanic/Latino
Country of Origin USA
Family Member 5
Family History N
Relation to Proband uncle
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Clinically affected; distal myopathy, generalized; muscle biopsy indicated inclusion body myopathy; co-segregation analysis results and confirmation by automated Sanger sequencing revealed a maternally inherited heterozygous mutation in the HSPB8 gene: c.515dupC (p.P173Sfs*43) in exon CDS 3; positive family history: this mutation is also present in the affected nephew (lymph GM26095, fibro GM26096) and affected sister (lymph GM26097, fibro GM26098); heterozygous variants of uncertain significance (VUS) that are present in both the affected son and affected brother are: CCDC78 c.986T>C (p.I329T), MUSK c.43C>A (p.L15M), and TRIM32 c.1223G>A (p.R408H); at-risk half-sister (GM26100-lymph); assistive device: wheelchair; pedigree and family history in PMID 31403083.

Characterizations

back to top
PDL at Freeze 5.62
Passage Frozen 7
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene HSPB8
Chromosomal Location 12q24.23
Allelic Variant 1 p.P173Sfs*43; MYOPATHY, MYOFIBRILLAR, 13, WITH RIMMED VACUOLES; MFM13
Identified Mutation c.515dupC (p.P173Sfs*43)

Phenotypic Data

back to top
Remarks Clinically affected; distal myopathy, generalized; muscle biopsy indicated inclusion body myopathy; co-segregation analysis results and confirmation by automated Sanger sequencing revealed a maternally inherited heterozygous mutation in the HSPB8 gene: c.515dupC (p.P173Sfs*43) in exon CDS 3; positive family history: this mutation is also present in the affected nephew (lymph GM26095, fibro GM26096) and affected sister (lymph GM26097, fibro GM26098); heterozygous variants of uncertain significance (VUS) that are present in both the affected son and affected brother are: CCDC78 c.986T>C (p.I329T), MUSK c.43C>A (p.L15M), and TRIM32 c.1223G>A (p.R408H); at-risk half-sister (GM26100-lymph); assistive device: wheelchair; pedigree and family history in PMID 31403083.

Publications

back to top
Al-Tahan S, Weiss L, Yu H, Tang S, Saporta M, Vihola A, Mozaffar T, Udd B, Kimonis V, New family with HSPB 8-associated autosomal dominant rimmed vacuolar myopathy Neurology Genetics5:e349 2018
PubMed ID: 31403083

External Links

back to top
Gene Cards HSPB8
Gene Ontology GO:0004674 protein serine/threonine kinase activity
GO:0006457 protein folding
GO:0006986 response to unfolded protein
GO:0008372 cellular_component unknown
GO:0016740 transferase activity
GO:0051082 unfolded protein binding
NCBI Gene Gene ID:26353
NCBI GTR 608014 HEAT-SHOCK 22-KD PROTEIN 8; HSPB8
621078 MYOPATHY MYOFIBRILLAR 13 WITH RIMMED VACUOLES; MFM13
OMIM 608014 HEAT-SHOCK 22-KD PROTEIN 8; HSPB8
621078 MYOPATHY MYOFIBRILLAR 13 WITH RIMMED VACUOLES; MFM13

Culture Protocols

back to top
Passage Frozen 7
Split Ratio 1:2
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
Add to Cart
How to Order
  • Ordering Instructions
  • MTA / Assurance Form
  • Statement of Research Intent Form
Related Products
Same Subject
  • GM28861 - Stem cell
Same Family
  • 3328
Miscellaneous
  • DNA on Demand
  • Custom Services

Our mission is to prevent and cure disease through biomedical research.

CONTACT US

CUSTOMER SERVICE
customerservice@coriell.org (800) 752-3805 • (856) 757-4848
Subscribe to our newsletter here

Coriell Institute for Medical Research
403 Haddon Avenue Camden, NJ 08103, USA (856) 966-7377

Ⓒ 2025 Coriell Institute. All rights reserved.

  • Facebook
  • Linkedin
  • Youtube