ID   HPSI0316i-muwv_3
AC   CVCL_IX77
SY   WTSIi448-A
DR   BioSamples; SAMEA4448534
DR   ECACC; 77650502
DR   HipSci; HPSI0316i-muwv_3
DR   hPSCreg; WTSIi448-A
DR   Wikidata; Q54890639
CC   From: University College London; London; United Kingdom.
CC   From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
CC   Population: Asian.
CC   Omics: Deep exome analysis.
CC   Omics: Transcriptome analysis by 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_IX78 ! HPSI0316i-muwv_6
SX   Male
AG   40-44Y
CA   Induced pluripotent stem cell
DT   Created: 15-05-17; Last updated: 29-06-23; Version: 12
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