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Cellosaurus GM29378 (CVCL_F0Z9)

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Cell line name GM29378
Synonyms GM29378*C
Accession CVCL_F0Z9
Resource Identification Initiative To cite this cell line use: GM29378 (RRID:CVCL_F0Z9)
Comments Population: Jewish; Ashkenazi.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:11164; SNRPN; Simple; p.Arg25Ter (c.73C>T); Zygosity=Heterozygous; Note=De novo mutation (Coriell=GM29378).
Disease Prader-Willi syndrome (NCIt: C75463)
Prader-Willi syndrome (ORDO: Orphanet_739)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_C7L4 (GM27891)
Sex of cell Female
Age at sampling 10Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; GM29378
Entry history
Entry creation27-Nov-2025
Last entry update27-Nov-2025
Version number1