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Cellosaurus UKHGi002-B (CVCL_A1QH)

[Text version]
Cell line name UKHGi002-B
Synonyms F-PKE (3)
Accession CVCL_A1QH
Resource Identification Initiative To cite this cell line use: UKHGi002-B (RRID:CVCL_A1QH)
Comments From: Institute of Human Genetics, University Hospital Heidelberg; Heidelberg; Germany.
Population: Caucasian; German.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_A1QG ! UKHGi002-A
Sex of cell Male
Age at sampling 55Y
Category Induced pluripotent stem cell
Publications

PubMed=33002717; DOI=10.1016/j.scr.2020.102004
Cristian F.-B., Koppel A., Janssen J.W.G., Utikal J.S., Rappold G.A., Berkel S.
Generation of two hiPSC lines from a patient with autism spectrum disorder harboring a 120 kb deletion in SHANK2 and two control lines from each parent.
Stem Cell Res. 49:102004-102004(2020)

Cross-references
Cell line databases/resources hPSCreg; UKHGi002-B
Biological sample resources BioSamples; SAMEA7390808
Encyclopedic resources Wikidata; Q102115066
Entry history
Entry creation29-Oct-2020
Last entry update05-Oct-2023
Version number6