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Cellosaurus GM17926 (CVCL_DA60)

[Text version]
Cell line name GM17926
Accession CVCL_DA60
Resource Identification Initiative To cite this cell line use: GM17926 (RRID:CVCL_DA60)
Comments Population: Caucasian.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; HGNC:7897; NPC1; Simple; p.Tyr509Ser (c.1526A>C); ClinVar=VCV000554002; Zygosity=Heterozygous (Coriell=GM17926).
  • Mutation; HGNC; HGNC:7897; NPC1; Simple; p.Ile1061Thr (c.3182T>C); ClinVar=VCV000002967; Zygosity=Heterozygous (Coriell=GM17926).
Disease Niemann-Pick disease, type C1 (NCIt: C126864)
Niemann-Pick disease type C (ORDO: Orphanet_646)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Children
Category Finite cell line
Publications

PubMed=12955717; DOI=10.1002/humu.10255
Park W.D., O'Brien J.F., Lundquist P.A., Kraft D.L., Vockley C.W., Karnes P.S., Patterson M.C., Snow K.
Identification of 58 novel mutations in Niemann-Pick disease type C: correlation with biochemical phenotype and importance of PTC1-like domains in NPC1.
Hum. Mutat. 22:313-325(2003)

Cross-references
Cell line collections (Providers) Coriell; GM17926
Cell line databases/resources CLO; CLO_0016274
Encyclopedic resources Wikidata; Q54849327
Entry history
Entry creation13-Jul-2016
Last entry update19-Dec-2024
Version number12