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Cellosaurus STJUDEi005-A (CVCL_C6SV)

[Text version]
Cell line name STJUDEi005-A
Synonyms INS14
Accession CVCL_C6SV
Resource Identification Initiative To cite this cell line use: STJUDEi005-A (RRID:CVCL_C6SV)
Comments From: St. Jude Children's Research Hospital; Memphis; USA.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:10402; RPS19; Simple; p.Arg62Trp (c.184C>T); ClinVar=VCV000006314; Zygosity=Heterozygous (hPSCreg=STJUDEi005-A).
Disease Congenital pure red cell aplasia (NCIt: C61236)
Blackfan-Diamond anemia (ORDO: Orphanet_124)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_C6SW (STJUDEi005-A-1)
Sex of cell Female
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; STJUDEi005-A
Biological sample resources BioSamples; SAMEA111437016
Encyclopedic resources Wikidata; Q117704900
Entry history
Entry creation21-Mar-2023
Last entry update19-Dec-2024
Version number5