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Cellosaurus IBBISTi004-B (CVCL_B7GT)

[Text version]
Cell line name IBBISTi004-B
Synonyms iPSC AS-GB clone 20; AS-GB clone 20
Accession CVCL_B7GT
Resource Identification Initiative To cite this cell line use: IBBISTi004-B (RRID:CVCL_B7GT)
Comments From: Simao Jose Teixeira da Rocha; Porto Salvo; Portugal.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Angelman syndrome (NCIt: C75462)
Angelman syndrome (ORDO: Orphanet_72)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_B7GS ! IBBISTi004-A
CVCL_B7GU ! IBBISTi004-C
Sex of cell Female
Age at sampling 3Y
Category Induced pluripotent stem cell
Publications

PubMed=35339881; DOI=10.1016/j.scr.2022.102757
Maranga C., Pereira C.A., Raposo A.C., Vieira A., Duarte S., Bekman E.P., Milagre I., da Rocha S.J.T.
Generation and characterization of induced pluripotent stem cell line (IBBISTi004-A) from an Angelman syndrome patient carrying a class II deletion of the maternal chromosome 15q11.2-q13.
Stem Cell Res. 61:102757-102757(2022)

Cross-references
Cell line databases/resources hPSCreg; IBBISTi004-B
Biological sample resources BioSamples; SAMEA13019138
Encyclopedic resources Wikidata; Q112929810
Entry history
Entry creation23-Jun-2022
Last entry update30-Jan-2024
Version number5