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Cellosaurus GM29256 (CVCL_D6WT)

[Text version]
Cell line name GM29256
Synonyms GM29256*B
Accession CVCL_D6WT
Resource Identification Initiative To cite this cell line use: GM29256 (RRID:CVCL_D6WT)
Comments Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:6884; MAPK8IP3; Simple; c.2451+1G>A; Zygosity=Unspecified; Note=Splice donor mutation (Coriell=GM29256).
Disease Neurodevelopmental disorder with or without variable brain abnormalities (NCIt: C206532)
Non-specific syndromic intellectual disability (ORDO: Orphanet_528084)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; GM29256
Entry history
Entry creation10-Sep-2024
Last entry update19-Dec-2024
Version number2