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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; 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
Shuai Li, Hui-Fang Zhao, Rong-Qi Huang, Lang He, Chao Tian, Hua-Lin Huang, Xiao-Bo Han, Feng Tang, Zuo-Xian Lin, Si-Hao Deng, Jian-Da Zhou, Zhi-Yuan Li;
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 update19-Dec-2024
Version number8