GM26117
LCL from B-Lymphocyte
Description:
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION; CFTD
ACTIN, ALPHA-1, SKELETAL MUSCLE; ACTA1
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases Muscular Dystrophies CMD Specific PIGI Consented Sample |
Biopsy Source
|
Peripheral vein
|
Cell Type
|
B-Lymphocyte
|
Tissue Type
|
Blood
|
Transformant
|
Epstein-Barr Virus
|
Sample Source
|
LCL from B-Lymphocyte
|
Race
|
White
|
Ethnicity
|
Lithuanian
|
Country of Origin
|
LITHUANIA
|
Family History
|
N
|
Relation to Proband
|
proband
|
Confirmation
|
Molecular characterization before cell line submission to CCR
|
ISCN
|
46,XX[33].arr(1-22,X)x2
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by LINE assay |
|
Gene |
ACTA1 |
Chromosomal Location |
1q42.13 |
Allelic Variant 1 |
; |
Identified Mutation |
ASN94LYS |
Remarks |
Clinically affected; donor is heterozygous for a pathogenic mutation in the ACTA1 gene (c.282C>A, p.N94K); donor also heterozygous for the following genetic variants that are not currently associated with the donor's phenotype: RYR1 gene (c.9635A>G, p.E3212G), OPA1 gene (c.1146A>G, p.I382M), and TK2 gene (c.547C>T, p.R183W); normal MRI brain scan; the following motor functions were never achieved: holding head up, sitting, walking or running without assistance; Karyotype was normal, with 2 cells with multiple random chromosome gain. |
Gene Cards |
ACTA1 |
Gene Ontology |
GO:0003774 motor activity |
|
GO:0005200 structural constituent of cytoskeleton |
|
GO:0005884 actin filament |
|
GO:0006936 muscle contraction |
|
GO:0007517 muscle development |
NCBI Gene |
Gene ID:4349 |
|
Gene ID:58 |
NCBI GTR |
102610 ACTIN, ALPHA, SKELETAL MUSCLE 1; ACTA1 |
|
255310 MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION; CFTD |
OMIM |
102610 ACTIN, ALPHA, SKELETAL MUSCLE 1; ACTA1 |
|
255310 MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION; CFTD |
Omim Description |
FIBER-TYPE DISPROPORTION MYOPATHY, CONGENITAL; CFTDM |
|
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION |
Split Ratio |
1:3 |
Temperature |
37 C |
Percent CO2 |
5% |
Percent O2 |
AMBIENT |
Medium |
Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not Inactivated |
Substrate |
None specified |
Subcultivation Method |
dilution - add fresh medium |
Supplement |
- |
|
|