Cellosaurus cell line iPSc-GD-C21 (CVCL

Cellosaurus iPSc-GD-C21 (CVCL_IN11)

Cross-references
Cell line name	iPSc-GD-C21
Synonyms	GD iPSC C21; Gaucher iPSC-C21; C21; 21C
Accession	CVCL_IN11
Resource Identification Initiative	To cite this cell line use: iPSc-GD-C21 (RRID:CVCL_IN11)
Comments	Omics: Transcriptomics; Microarray. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:4177; GBA1; Simple; p.Gly241Arg (c.721G>A) (G202R); ClinVar=VCV000093459; Zygosity=Heterozygous (PubMed=23118351). Mutation; HGNC; HGNC:4177; GBA1; Simple; p.Leu483Pro (c.1448T>C) (L444P); ClinVar=VCV000004288; Zygosity=Heterozygous (PubMed=23118351).
Disease	Gaucher disease (NCIt: C61268) Gaucher disease (ORDO: Orphanet_355)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_IN10 ! iPSc-GD-A8
Sex of cell	Male
Age at sampling	Age unspecified
Category	Induced pluripotent stem cell
Publications	PubMed=23118351; DOI=10.1093/hmg/dds471 Gustavo Tiscornia, Erika Lorenzo Vivas, Leslie Matalonga, Ina Berniakovich, Montserrat Barragan Monasterio, Cristina Eguizabal Argaiz, Laura Gort, Federico Gonzalez, Carmen Ortiz Mellet, Jose Manuel Garcia-Fernandez, Antonia Ribes ...Show all 13 authors... , Anna Veiga, Juan Carlos Izpisua Belmonte; Show fewer authors Neuronopathic Gaucher's disease: induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds. Hum. Mol. Genet. 22:633-645(2013)
Encyclopedic resources	Wikidata; Q54898225
Gene expression databases	GEO; GSM1012128
Entry history
Entry creation	01-Dec-2016
Last entry update	10-Apr-2025
Version number	17