Cellosaurus cell line CLN3-iPS 1A (CVCL

Cellosaurus CLN3-iPS 1A (CVCL_VK57)

Cross-references
Cell line name	CLN3-iPS 1A
Accession	CVCL_VK57
Resource Identification Initiative	To cite this cell line use: CLN3-iPS 1A (RRID:CVCL_VK57)
Comments	Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:2074; CLN3; Simple; c.461-280_677+382del (1.02-kb del); ClinVar=VCV000003552; Zygosity=Homozygous (PubMed=24271013).
Disease	Neuronal ceroid lipofuscinosis type 3 (NCIt: C61258) Congenital neuronal ceroid lipofuscinosis (ORDO: Orphanet_168486)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_VK58 ! CLN3-iPS 1B
Sex of cell	Male
Age at sampling	Age unspecified
Category	Induced pluripotent stem cell
Publications	PubMed=24271013; DOI=10.1093/hmg/ddt596; PMCID=PMC3959814 Xenia Lojewski, John F. Staropoli, Sunita Biswas-Legrand, Alexandra M. Simas, Larissa Haliw, Martin K. Selig, Scott H. Coppel, Kendrick A. Goss, Anton Petcherski, Uma Chandrachud, Steven D. Sheridan ...Show all 23 authors... , Diane E. Lucente, Katherine B. Sims, James Francis Gusella, Dolan Sondhi, Ronald G. Crystal, Peter Reinhardt, Jared Sterneckert, Hans Robert Scholer, Stephen John Haggarty, Alexander Storch, Andreas Hermann, Susan L. Cotman; Show fewer authors 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; Q93454896
Entry history
Entry creation	07-Sep-2018
Last entry update	19-Dec-2024
Version number	11