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Cellosaurus SDQLCHi014-A (CVCL_YI67)

[Text version]
Cell line name SDQLCHi014-A
Accession CVCL_YI67
Resource Identification Initiative To cite this cell line use: SDQLCHi014-A (RRID:CVCL_YI67)
Comments From: Qilu Children's Hospital of Shandong University; Jinan; China.
Population: Chinese; Han.
Derived from site: In situ; Urine; UBERON=UBERON_0001088.
Sequence variations
  • Mutation; HGNC; HGNC:4599; GRM7; Unexplicit; Ex3-7del; Zygosity=Heterozygous; Note=De novo mutation (PubMed=31707215).
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 5Y
Category Induced pluripotent stem cell
Publications

PubMed=31707215; DOI=10.1016/j.scr.2019.101635
Yang X.-M., Liu Y., Zhou T.-C., Zhang H.-Y., Dong R., Li Y., Liu N., Liu Y., Gai Z.-T.
An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303kb de novo deletion at chr3p26.1 implicating GRM7 gene.
Stem Cell Res. 41:101635-101635(2019)

Cross-references
Cell line databases/resources hPSCreg; SDQLCHi014-A
Encyclopedic resources Wikidata; Q98129475
Entry history
Entry creation19-Dec-2019
Last entry update19-Dec-2024
Version number8