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Cellosaurus STBCi028-B (CVCL_RB92)

[Text version]
Cell line name STBCi028-B
Synonyms SFC018-03-02
Accession CVCL_RB92
Resource Identification Initiative To cite this cell line use: STBCi028-B (RRID:CVCL_RB92)
Comments From: StemBANCC; Oxford; United Kingdom.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; 1388; CACNA1A; Simple; p.Arg582Gln (c.1745G>A) (p.Arg583Gln, c.1748G>A); ClinVar=VCV000008505; Zygosity=Heterozygous.
Disease Familial hemiplegic migraine-1 (NCIt: C189277)
Familial or sporadic hemiplegic migraine (ORDO: Orphanet_569)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_RB91 ! STBCi028-A
CVCL_RB93 ! STBCi028-C
Sex of cell Female
Age at sampling 35-39Y
Category Induced pluripotent stem cell
Cell line collections (Providers) EBiSC; STBCi028-B
ECACC; 66540701 - Discontinued
Cell line databases/resources hPSCreg; STBCi028-B
Biological sample resources BioSamples; SAMEA104493667
Encyclopedic resources Wikidata; Q54956429
Entry history
Entry creation05-Mar-2018
Last entry update30-Jan-2024
Version number10