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Cellosaurus HPS1912 (CVCL_C9Q0)

[Text version]
Cell line name HPS1912
Accession CVCL_C9Q0
Resource Identification Initiative To cite this cell line use: HPS1912 (RRID:CVCL_C9Q0)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease 1p36 deletion syndrome (NCIt: C74983)
1p36 deletion syndrome (ORDO: Orphanet_1606)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_C9Q1 ! HPS1913
CVCL_C9Q2 ! HPS1914
CVCL_C9Q3 ! HPS1915
CVCL_C9Q4 ! HPS1916
CVCL_C9Q5 ! HPS1917
Sex of cell Male
Age at sampling 10-19Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS1912
Encyclopedic resources Wikidata; Q123031948
Entry history
Entry creation05-Oct-2023
Last entry update30-Jan-2024
Version number2