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Cellosaurus BCHi007-A (CVCL_D6RV)

[Text version]
Cell line name BCHi007-A
Synonyms HNDS0005-01 #B
Accession CVCL_D6RV
Resource Identification Initiative To cite this cell line use: BCHi007-A (RRID:CVCL_D6RV)
Comments From: Children's Hospital Boston; Boston; USA.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 408; ALDH5A1; Simple; p.Gly409Asp (c.1226G>A); ClinVar=VCV000001359; Zygosity=Homozygous (PubMed=38677032).
Disease Succinic semialdehyde dehydrogenase deficiency (NCIt: C206527)
Succinic semialdehyde dehydrogenase deficiency (ORDO: Orphanet_22)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_D6RW (BCHi007-A-1)
Sex of cell Female
Age at sampling 21Y
Category Induced pluripotent stem cell
Publications

PubMed=38677032; DOI=10.1016/j.scr.2024.103424; PMCID=PMC11178435
Afshar-Saber W., Chen C.-D., Teaney N.A., Kim K., Yang Z.-Q., Gasparoli F.M., Ebrahimi-Fakhari D., Buttermore E.D., Chen I.P.-F., Pearl P.L., Sahin M.
Generation and characterization of six human induced pluripotent stem cell lines (hiPSCs) from three individuals with SSADH deficiency and CRISPR-corrected isogenic controls.
Stem Cell Res. 77:103424-103424(2024)

Cross-references
Cell line databases/resources hPSCreg; BCHi007-A
Biological sample resources BioSamples; SAMEA115476580
Entry history
Entry creation10-Sep-2024
Last entry update10-Sep-2024
Version number1