ID   FRDA4230B
AC   CVCL_E6E6
SY   F4230B; 4230B
DR   ABM; T5478
CC   Part of: Friedreich's ataxia primary fibroblast repository.
CC   Sequence variation: Mutation; HGNC; HGNC:3951; FXN; Repeat_expansion; IVS1 GAA[567]; ClinVar=VCV000561195; Zygosity=Heterozygous (ABM=T5478).
CC   Sequence variation: Mutation; HGNC; HGNC:3951; FXN; Repeat_expansion; IVS1 GAA[744]; ClinVar=VCV000561195; Zygosity=Heterozygous (ABM=T5478).
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84718; Friedreich ataxia
DI   ORDO; Orphanet_95; Friedreich ataxia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_ZB98 ! FRDA4230
SX   Female
AG   34Y
CA   Finite cell line
DT   Created: 10-04-25; Last updated: 10-04-25; Version: 1
//