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Cellosaurus BCHi006-B (CVCL_A7KK)

[Text version]

Cell line name BCHi006-B
Synonyms MAN0855-01 #D
Accession CVCL_A7KK
Resource Identification Initiative To cite this cell line use: BCHi006-B (RRID:CVCL_A7KK)
Comments From: Children's Hospital Boston; Boston; USA.
Derived from sampling site: Skin; dermis.
Sequence variations Mutation; HGNC; 11411; CDKL5; Simple; p.Asp471Glufs*37 (c.1412delA); Zygosity=Heterozygous (PubMed=33714067).
Disease Early infantile 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_A7KJ ! BCHi006-A
Sex of cell Female
Age at sampling 3Y
Category Induced pluripotent stem cell

PubMed=33714067; DOI=10.1016/j.scr.2021.102276
Chen 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)

Cell line databases/resources hPSCreg; BCHi006-B
Other Wikidata; Q107113448
Entry history
Entry creation20-May-2021
Last entry update23-Sep-2021
Version number2