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Cellosaurus UCLi006-A (CVCL_VF11)

[Text version]
Cell line name UCLi006-A
Synonyms LCMD-L302P-UCL01C2
Accession CVCL_VF11
Resource Identification Initiative To cite this cell line use: UCLi006-A (RRID:CVCL_VF11)
Comments From: University College London; London; United Kingdom.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:6636; LMNA; Simple; p.Leu302Pro (c.905T>C); ClinVar=VCV000066953; Zygosity=Heterozygous (hPSCreg=UCLi006-A).
Disease Muscular dystrophy congenital, LMNA-related (NCIt: C148369)
Congenital muscular dystrophy due to LMNA mutation (ORDO: Orphanet_157973)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; UCLi006-A
ECACC; 66540593 - Discontinued
Cell line databases/resources hPSCreg; UCLi006-A
Biological sample resources BioSamples; SAMEA104130970
Encyclopedic resources Wikidata; Q54989674
Entry history
Entry creation14-May-2018
Last entry update19-Dec-2024
Version number12