Cellosaurus cell line CRICKi007-A (CVCL

Cross-references
Cell line name	CRICKi007-A
Synonyms	iFCI009
Accession	CVCL_C3R2
Resource Identification Initiative	To cite this cell line use: CRICKi007-A (RRID:CVCL_C3R2)
Comments	From: The Francis Crick Institute Limited; London; United Kingdom. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:17208; BICD2; Simple; p.Ile189Phe (c.565A>T); ClinVar=VCV000637065; Zygosity=Heterozygous (PubMed=36332468).
Disease	Autosomal dominant childhood-onset lower extremity-predominant spinal muscular atrophy-2A (NCIt: C191766) BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy (ORDO: Orphanet_363454)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Female
Age at sampling	11Y
Category	Induced pluripotent stem cell
Publications	PubMed=36332468; DOI=10.1016/j.scr.2022.102954 Devito L.G., Cooper F., D'Angelo I., Smith J., Healy L.E. Generation of four iPSC lines (CRICKi004-A; CRICKi005-A; CRICKi006-A, CRICKi007-A) from spinal muscle atrophy patients with lower extremity dominant (SMALED) phenotype. Stem Cell Res. 65:102954-102954(2022)
Cell line databases/resources	hPSCreg; CRICKi007-A
Biological sample resources	BioSamples; SAMEA112227670
Encyclopedic resources	Wikidata; Q116048790
Entry history
Entry creation	15-Dec-2022
Last entry update	19-Dec-2024
Version number	5