Cellosaurus cell line RCMGi002-A (CVCL

Cross-references
Cell line name	RCMGi002-A
Synonyms	P7L2
Accession	CVCL_YT37
Resource Identification Initiative	To cite this cell line use: RCMGi002-A (RRID:CVCL_YT37)
Comments	From: Research Centre for Medical Genetics; Moscow; Russia. Population: Caucasian. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:1884; CFTR; Simple; p.Phe508del (c.1521_1523delCTT); ClinVar=VCV000007105; Zygosity=Homozygous (PubMed=33684631).
Disease	Cystic fibrosis (NCIt: C2975) Cystic fibrosis (ORDO: Orphanet_586)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Female
Age at sampling	24Y
Category	Induced pluripotent stem cell
Publications	PubMed=33684631; DOI=10.1016/j.scr.2021.102251 Kondrateva E.V., Demchenko A.G., Slesarenko Y.S., Yasinovsky M., Amelina E., Tabakov V.Y., Voronina E.S., Lavrov A.V., Smirnikhina S.A. Derivation of iPSC line (RCMGi002-A) from dermal fibroblasts of a cystic fibrosis female patient with homozygous F508del mutation. Stem Cell Res. 53:102251-102251(2021)
Cell line databases/resources	hPSCreg; RCMGi002-A
Biological sample resources	BioSamples; SAMEA6703339
Encyclopedic resources	Wikidata; Q98128872
Entry history
Entry creation	12-Mar-2020
Last entry update	19-Dec-2024
Version number	7