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Cellosaurus SJTUXHi002-A (CVCL_C0F7)

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Cell line name SJTUXHi002-A
Accession CVCL_C0F7
Resource Identification Initiative To cite this cell line use: SJTUXHi002-A (RRID:CVCL_C0F7)
Comments From: Shanghai Xinhua Hospital, Shanghai Jiao Tong University; Shanghai; China.
Population: Chinese; Han.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:4572; GRIA2; Simple; c.1998delT; Zygosity=Heterozygous (PubMed=35134694).
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 8Y
Category Induced pluripotent stem cell
Publications

PubMed=35134694; DOI=10.1016/j.scr.2022.102676
Yong Ji, Hui Lv, Zi-Lin Chen, Jue-Hua Yu, Shuan-Feng Fang, Fei Li;
Generation of a human induced pluripotent stem cell line (SJTUXHi002-A) from an individual with autism spectrum disorder carrying a heterozygous mutation in GRIA2.
Stem Cell Res. 60:102676-102676(2022)

Cross-references
Cell line databases/resources hPSCreg; SJTUXHi002-A
Biological sample resources BioSamples; SAMEA11567037
Encyclopedic resources Wikidata; Q112930397
Entry history
Entry creation23-Jun-2022
Last entry update19-Dec-2024
Version number5