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Cellosaurus GM27226 (CVCL_YN35)

[Text version]
Cell line name GM27226
Accession CVCL_YN35
Resource Identification Initiative To cite this cell line use: GM27226 (RRID:CVCL_YN35)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:9115; PMM2; Simple; p.Arg141His (c.422G>A); ClinVar=VCV000007706; Zygosity=Heterozygous (Coriell=GM27226).
  • Mutation; HGNC; HGNC:9115; PMM2; Simple; p.Asn216Ile (c.647A>T); ClinVar=VCV000007707; Zygosity=Heterozygous (Coriell=GM27226).
Disease Congenital disorder of glycosylation type Ia (NCIt: C126868)
PMM2-CDG (ORDO: Orphanet_79318)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 1Y
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; GM27226
Encyclopedic resources Wikidata; Q93933090
Entry history
Entry creation12-Mar-2020
Last entry update19-Dec-2024
Version number10