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Cellosaurus GM18455 (CVCL_DA79)

[Text version]
Cell line name GM18455
Accession CVCL_DA79
Resource Identification Initiative To cite this cell line use: GM18455 (RRID:CVCL_DA79)
Comments Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; 14537; NPC2; Simple; p.Glu20Ter (c.58G>T); ClinVar=VCV000008477; Zygosity=Heterozygous (Coriell=GM18455).
  • Mutation; HGNC; 14537; NPC2; Simple; p.Cys47Phe (c.140G>T); ClinVar=VCV000549984; Zygosity=Heterozygous (Coriell=GM18455).
Disease Niemann-Pick disease, type C2 (NCIt: C126865)
Niemann-Pick disease type C (ORDO: Orphanet_646)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_UL88 (AKOSi001-A)
Sex of cell Male
Age at sampling Age unspecified
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; GM18455
Cell line databases/resources CLO; CLO_0031138
Encyclopedic resources Wikidata; Q54849545
Entry history
Entry creation13-Jul-2016
Last entry update30-Jan-2024
Version number12