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Cellosaurus HPSI1016i-riwg_8 (CVCL_LM58)

[Text version]
Cell line name HPSI1016i-riwg_8
Synonyms WTSIi681-B; WTSIi712-A
Accession CVCL_LM58
Resource Identification Initiative To cite this cell line use: HPSI1016i-riwg_8 (RRID:CVCL_LM58)
Comments From: Cambridge BioResource; Cambridge; United Kingdom.
Population: Caucasian; Irish.
Donor information: Donor is said to be suffering from a 'rare genetic neurological disorder'.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Nervous system disorder (NCIt: C26835)
Rare genetic neurological disorder (ORDO: Orphanet_71859)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_LM57 ! HPSI1016i-riwg_2
Sex of cell Female
Age at sampling 5-9Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) ECACC; 77650796
Cell line databases/resources HipSci; HPSI1016i-riwg_8
hPSCreg; WTSIi681-B
Biological sample resources BioSamples; SAMEA104132682
Encyclopedic resources Wikidata; Q54891615
Entry history
Entry creation15-Nov-2017
Last entry update29-Jun-2023
Version number10