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Cellosaurus WFS2_1 (CVCL_A5DN)

[Text version]
Cell line name WFS2_1
Accession CVCL_A5DN
Resource Identification Initiative To cite this cell line use: WFS2_1 (RRID:CVCL_A5DN)
Comments Population: Caucasian; Italian.
Derived from site: In situ; Arm, skin, dermis; UBERON=UBERON_0002427+UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Wolfram syndrome (NCIt: C35133)
Wolfram syndrome (ORDO: Orphanet_3463)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_A4FJ (WFS2_1#10)CVCL_A4FK (WFS2_1#11)CVCL_A4FH (WFS2_1#2)
CVCL_A4FL (WFS2_1#24)CVCL_A4FI (WFS2_1#3)
Sex of cell Female
Age at sampling 19Y
Category Finite cell line
Web pages Provider; BioKryo; -; https://biokryo.airliquide.com/sites/biokryo/files/2022-07/human-fibroblasts-catalogue-isenet.pdf
Publications

PubMed=29239282; DOI=10.1089/scd.2017.0158
Alberto La Spada, Aikaterini Ntai, Stefano Genovese, Maurizio Rondinelli, Pasquale De Blasio, Ida Biunno;
Generation of human-induced pluripotent stem cells from Wolfram syndrome type 2 patients bearing the c.103 + 1G>A CISD2 mutation for disease modeling.
Stem Cells Dev. 27:287-295(2018)

Cross-references
Encyclopedic resources Wikidata; Q107117440
Entry history
Entry creation20-May-2021
Last entry update10-Apr-2025
Version number7