Cellosaurus cell line TPP1-iPS 1B (CVCL

Cellosaurus TPP1-iPS 1B (CVCL_VK67)

Cross-references
Cell line name	TPP1-iPS 1B
Accession	CVCL_VK67
Resource Identification Initiative	To cite this cell line use: TPP1-iPS 1B (RRID:CVCL_VK67)
Comments	Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:2073; TPP1; Simple; c.509-1G>C (IVS5-1G>C); ClinVar=VCV000002644; Zygosity=Heterozygous; Note=Splice acceptor mutation (PubMed=24271013). Mutation; HGNC; HGNC:2073; TPP1; Simple; p.Arg208Ter (c.622C>T); ClinVar=VCV000002643; Zygosity=Heterozygous (PubMed=24271013).
Disease	Neuronal ceroid lipofuscinosis type 2 (NCIt: C85864) Congenital neuronal ceroid lipofuscinosis (ORDO: Orphanet_168486)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_VK66 ! TPP1-iPS 1A CVCL_VK68 ! TPP1-iPS 1C
Sex of cell	Female
Age at sampling	Age unspecified
Category	Induced pluripotent stem cell
Publications	PubMed=24271013; DOI=10.1093/hmg/ddt596; PMCID=PMC3959814 Lojewski X., Staropoli J.F., Biswas-Legrand S., Simas A.M., Haliw L., Selig M.K., Coppel S.H., Goss K.A., Petcherski A., Chandrachud U., Sheridan S.D., Lucente D., Sims K.B., Gusella J.F., Sondhi D., Crystal R.G., Reinhardt P., Sterneckert J., Scholer H.R., Haggarty S.J., Storch A., Hermann A., Cotman S.L. Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathway. Hum. Mol. Genet. 23:2005-2022(2014)
Encyclopedic resources	Wikidata; Q98133522
Entry history
Entry creation	07-Sep-2018
Last entry update	19-Dec-2024
Version number	11