Cellosaurus cell line FRDA4192 (CVCL

Cross-references
Cell line name	FRDA4192
Synonyms	F4192
Accession	CVCL_ZB96
Resource Identification Initiative	To cite this cell line use: FRDA4192 (RRID:CVCL_ZB96)
Comments	Omics: Transcriptome analysis by RNAseq. Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:3951; FXN; Repeat_expansion; IVS1 GAA[400]; ClinVar=VCV000561195; Zygosity=Heterozygous (PubMed=29125828). Mutation; HGNC; HGNC:3951; FXN; Repeat_expansion; IVS1 GAA[967]; ClinVar=VCV000561195; Zygosity=Heterozygous (PubMed=29125828).
Disease	Friedreich ataxia (NCIt: C84718) Friedreich ataxia (ORDO: Orphanet_95)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	33Y
Category	Finite cell line
Publications	PubMed=29125828; DOI=10.1242/dmm.030536; PMCID=PMC5719256 Napierala J.S., Li Y.-J., Lu Y., Lin K., Hauser L.A., Lynch D.R., Napierala M. Comprehensive analysis of gene expression patterns in Friedreich's ataxia fibroblasts by RNA sequencing reveals altered levels of protein synthesis factors and solute carriers. Dis. Model. Mech. 10:1353-1369(2017)
Encyclopedic resources	Wikidata; Q98126249
Entry history
Entry creation	02-Jul-2020
Last entry update	19-Dec-2024
Version number	8