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Cellosaurus (CVCL_B0F2)

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Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Omics: Genomics; Whole genome sequencing.
Omics: Transcriptomics; RNAseq.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Methylmalonic acidemia (NCIt: C98986)
Methylmalonic acidemia without homocystinuria (ORDO: Orphanet_293355)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 7M
Category Finite cell line
Publications



Three novel mutations responsible for Cockayne syndrome group A.
Genes Genet. Syst. 78:93-102(2003)

Entry history
Entry creation16-Dec-2021
Last entry update10-Apr-2025
Version number5