ID   HPSI0216i-vieg_3
AC   CVCL_IX75
SY   WTSIi472-B; WTSIi547-A
DR   BioSamples; SAMEA4453872
DR   ECACC; 77650491
DR   HipSci; HPSI0216i-vieg_3
DR   hPSCreg; WTSIi472-B
DR   Wikidata; Q54890588
CC   From: University College London; London; United Kingdom.
CC   From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
CC   Population: Caucasian.
CC   Omics: Genomics; Whole exome sequencing.
CC   Omics: Proteomics.
CC   Omics: Transcriptomics; RNAseq.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C140268; Hereditary cerebellar ataxia
DI   ORDO; Orphanet_183518; Rare hereditary ataxia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_IX76 ! HPSI0216i-vieg_5
SX   Male
AG   40-44Y
CA   Induced pluripotent stem cell
DT   Created: 15-05-17; Last updated: 10-04-25; Version: 13
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