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Cellosaurus STJUDEi005-A-1 (CVCL_C6SW)

[Text version]
Cell line name STJUDEi005-A-1
Synonyms INS14 Isogenic
Accession CVCL_C6SW
Resource Identification Initiative To cite this cell line use: STJUDEi005-A-1 (RRID:CVCL_C6SW)
Comments From: St. Jude Children's Research Hospital; Memphis; USA.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 10402; RPS19; Simple_corrected; p.Arg62Trp (c.184C>T); ClinVar=VCV000006314; Zygosity=Heterozygous; Note=By CRISPR/Cas9 (hPSCreg=STJUDEi005-1).
Disease Congenital pure red cell aplasia (NCIt: C61236)
Blackfan-Diamond anemia (ORDO: Orphanet_124)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_C6SV (STJUDEi005-A)
Sex of cell Female
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; STJUDEi005-A-1
Biological sample resources BioSamples; SAMEA111437018
Encyclopedic resources Wikidata; Q117704901
Entry history
Entry creation21-Mar-2023
Last entry update29-Jun-2023
Version number2