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Cellosaurus BCHi003-A (CVCL_A7KD)

[Text version]
Cell line name BCHi003-A
Synonyms HNDS0059-01 #A
Accession CVCL_A7KD
Resource Identification Initiative To cite this cell line use: BCHi003-A (RRID:CVCL_A7KD)
Comments From: Children's Hospital Boston; Boston; USA.
Population: Caucasian.
Characteristics: Established from a patient that is mosaic for a CDKL5 p.Leu629Ter mutation, but this cell line does not contain this mutation.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Developmental and epileptic encephalopathy 2 (NCIt: C147070)
CDKL5-related epileptic encephalopathy (ORDO: Orphanet_505652)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_A7KE ! BCHi003-B
Sex of cell Male
Age at sampling 2Y11M
Category Induced pluripotent stem cell
Publications

PubMed=33714067; DOI=10.1016/j.scr.2021.102276; PMCID=PMC8953930
Chen I.P.-F., Chen T., Forman T.E., Swanson A.C., O'Kelly B., Dwyer S.A., Buttermore E.D., Kleiman R., Carrington S.J.S., Lavery D.J., Swanson L.C., Olson H.E., Sahin M.
Generation and characterization of human induced pluripotent stem cells (iPSCs) from three male and three female patients with CDKL5 deficiency disorder (CDD).
Stem Cell Res. 53:102276-102276(2021)

Cross-references
Cell line databases/resources hPSCreg; BCHi003-A
Encyclopedic resources Wikidata; Q107113440
Entry history
Entry creation20-May-2021
Last entry update29-Jun-2023
Version number5