Cellosaurus cell line AIBNi017-A (CVCL

Cross-references
Cell line name	AIBNi017-A
Synonyms	SPGh1-S075mC2
Accession	CVCL_C1SM
Resource Identification Initiative	To cite this cell line use: AIBNi017-A (RRID:CVCL_C1SM)
Comments	From: Australian Institute for Bioengineering and Nanotechnology; Brisbane; Australia. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations	Mutation; HGNC; HGNC:20582; CYP2U1; Simple; p.Ile158Serfs*2 (c.471delC); ClinVar=VCV000655971; Zygosity=Heterozygous (PubMed=36166872).
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Female
Age at sampling	34Y
Category	Induced pluripotent stem cell
Publications	PubMed=36166872; DOI=10.1016/j.scr.2022.102917 Leeson H.C., Goh D., Coman D., Wolvetang E.J. Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations. Stem Cell Res. 64:102917-102917(2022)
Cell line databases/resources	hPSCreg; AIBNi017-A
Biological sample resources	BioSamples; SAMEA111323977
Encyclopedic resources	Wikidata; Q114310552
Entry history
Entry creation	22-Sep-2022
Last entry update	19-Dec-2024
Version number	5