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Cellosaurus USCi004-A (CVCL_UL42)

[Text version]
Cell line name USCi004-A
Synonyms iBFLS2; 26B
Accession CVCL_UL42
Resource Identification Initiative To cite this cell line use: USCi004-A (RRID:CVCL_UL42)
Comments From: University of Southern California, Los Angeles; Los Angeles; USA.
Sequence variations
  • Mutation; HGNC; 18145; PHF6; Simple; p.Cys45Tyr (c.134G>A); ClinVar=VCV000011066; Zygosity=Unspecified.
Disease Mental retardation, X-linked, syndromic, Borjeson-Forssman-Lehmann type (NCIt: C157122)
Borjeson-Forssman-Lehmann syndrome (ORDO: Orphanet_127)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; USCi004-A
Encyclopedic resources Wikidata; Q98134365
Entry history
Entry creation25-Feb-2019
Last entry update21-Mar-2023
Version number6