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Cellosaurus HPS2031 (CVCL_C9VB)

[Text version]
Cell line name HPS2031
Accession CVCL_C9VB
Resource Identification Initiative To cite this cell line use: HPS2031 (RRID:CVCL_C9VB)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 438; ALPL; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS2031).
Disease Hypophosphatasia (NCIt: C26798)
Hypophosphatasia (ORDO: Orphanet_436)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_C9VA ! HPS2030
CVCL_C9VC ! HPS2032
CVCL_C9VD ! HPS2033
CVCL_C9VE ! HPS2034
CVCL_C9VF ! HPS2035
Sex of cell Female
Age at sampling 1-5Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS2031
Encyclopedic resources Wikidata; Q123032022
Entry history
Entry creation05-Oct-2023
Last entry update30-Jan-2024
Version number2