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Cellosaurus AIBNi018-A (CVCL_C1SN)

[Text version]
Cell line name AIBNi018-A
Synonyms SPGh2-S964pC6
Accession CVCL_C1SN
Resource Identification Initiative To cite this cell line use: AIBNi018-A (RRID:CVCL_C1SN)
Comments From: Australian Institute for Bioengineering and Nanotechnology; Brisbane; Australia.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 20582; CYP2U1; Simple; p.Leu362Pro (c.1085T>C); Zygosity=Heterozygous (PubMed=36166872).
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 37Y
Category Induced pluripotent stem cell

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; AIBNi018-A
Biological sample resources BioSamples; SAMEA111323979
Encyclopedic resources Wikidata; Q114310555
Entry history
Entry creation22-Sep-2022
Last entry update29-Jun-2023
Version number4