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Cellosaurus CHD-39 (CVCL_ZW20)

[Text version]
Cell line name CHD-39
Synonyms iPSC.3
Accession CVCL_ZW20
Resource Identification Initiative To cite this cell line use: CHD-39 (RRID:CVCL_ZW20)
Comments From: National Human Genome Research Institute; Bethesda; USA.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:1968; LYST; Simple; p.Val1564_Arg1621del (c.4862+1G>A) (c.4689_4862del); Zygosity=Heterozygous (PubMed=32619719).
  • Mutation; HGNC; HGNC:1968; LYST; Simple; p.His3236Tyr (c.9706C>T); Zygosity=Heterozygous (PubMed=32619719).
Disease Chediak-Higashi syndrome (NCIt: C2941)
Chediak-Higashi syndrome (ORDO: Orphanet_167)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 4Y
Category Induced pluripotent stem cell
Publications

PubMed=32619719; DOI=10.1016/j.scr.2020.101883
Serra-Vinardell J., Sandler M.B., Pak E., Zheng W., Dutra A., Introne W., Gahl W.A., Malicdan M.C.V.
Generation and characterization of four Chediak-Higashi syndrome (CHS) induced pluripotent stem cell (iPSC) lines.
Stem Cell Res. 47:101883-101883(2020)

Cross-references
Encyclopedic resources Wikidata; Q102113675
Entry history
Entry creation29-Oct-2020
Last entry update19-Dec-2024
Version number6