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Cellosaurus GM29608 (CVCL_F0ZN)

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Cell line name GM29608
Synonyms GM29608*B
Accession CVCL_F0ZN
Resource Identification Initiative To cite this cell line use: GM29608 (RRID:CVCL_F0ZN)
Comments Population: Caucasian.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; HGNC:14214; CIC; Simple; p.Arg1262Ter (c.3784C>T) (p.Arg353Ter, c.1057C>T); ClinVar=VCV000431168; Zygosity=Heterozygous (Coriell=GM29608).
Disease Intellectual developmental disorder, autosomal dominant 45 (NCIt: C222355)
Autosomal dominant non-syndromic intellectual disability (ORDO: Orphanet_178469)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Children
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; GM29608
Entry history
Entry creation27-Nov-2025
Last entry update27-Nov-2025
Version number1