Cellosaurus cell line NPC1-2#9 (CVCL

Cross-references
Cell line name	NPC1-2#9
Synonyms	WIBR-IPS-NPC1P237S/I1061T #9
Accession	CVCL_RM42
Resource Identification Initiative	To cite this cell line use: NPC1-2#9 (RRID:CVCL_RM42)
Comments	Population: Caucasian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:7897; NPC1; Simple; p.Pro237Ser (c.709C>T); ClinVar=VCV000021142; Zygosity=Heterozygous (PubMed=24936472). Mutation; HGNC; HGNC:7897; NPC1; Simple; p.Ile1061Thr (c.3182T>C); ClinVar=VCV000002967; Zygosity=Heterozygous (PubMed=24936472).
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)
Hierarchy	Parent: CVCL_7374 (GM03123)
Sex of cell	Female
Age at sampling	9Y
Category	Induced pluripotent stem cell
Publications	PubMed=24936472; DOI=10.1016/j.stemcr.2014.03.014; PMCID=PMC4050353 Maetzel D., Sarkar S., Wang H., Abi-Mosleh L., Xu P., Cheng A.W., Gao Q., Mitalipova M., Jaenisch R. Genetic and chemical correction of cholesterol accumulation and impaired autophagy in hepatic and neural cells derived from Niemann-Pick type C patient-specific iPS cells. Stem Cell Reports 2:866-880(2014)
Cell line databases/resources	SKIP; SKIP000696
Encyclopedic resources	Wikidata; Q54930985
Entry history
Entry creation	05-Mar-2018
Last entry update	19-Dec-2024
Version number	10