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Cellosaurus GIBHi001-A (CVCL_XJ81)

[Text version]
Cell line name GIBHi001-A
Synonyms ASD-hiPSC
Accession CVCL_XJ81
Resource Identification Initiative To cite this cell line use: GIBHi001-A (RRID:CVCL_XJ81)
Comments From: Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences; Guangzhou; China.
Derived from site: In situ; Urine; UBERON=UBERON_0001088.
Sequence variations
  • Mutation; HGNC; 3614; FCGR1BP; Simple; p.Arg139Ter (c.415C>T); Zygosity=Heterozygous (PubMed=31520889).
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 16Y
Category Induced pluripotent stem cell
Publications

PubMed=31520889; DOI=10.1016/j.scr.2019.101571
Li S., Zhao H.-F., Huang R.-Q., He L., Tian C., Huang H.-L., Han X.-B., Tang F., Lin Z.-X., Deng S.-H., Zhou J.-D., Li Z.-Y.
Generation of iPSC line (GIBHi001-A) from a patient with autism spectrum disorder.
Stem Cell Res. 40:101571-101571(2019)

Cross-references
Cell line databases/resources hPSCreg; GIBHi001-A
SKIP; SKIP005559
Biological sample resources BioSamples; SAMEA5928136
Encyclopedic resources Wikidata; Q93561133
Entry history
Entry creation19-Dec-2019
Last entry update29-Jun-2023
Version number7