Home  |  Contact

Cellosaurus HPS2040 (CVCL_A3HN)

Cell line name HPS2040
Accession CVCL_A3HN
Resource Identification Initiative To cite this cell line use: HPS2040 (RRID:CVCL_A3HN)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 1037; CFB; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS2040).
Disease Atypical hemolytic uremic syndrome-4 (NCIt: C176902)
Atypical hemolytic uremic syndrome (ORDO: Orphanet_2134)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_A3HJ ! HPS2036
CVCL_A3HK ! HPS2037
CVCL_A3HL ! HPS2038
CVCL_A3HM ! HPS2039
CVCL_A3HP ! HPS2041
Sex of cell Female
Age at sampling 10-19Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS2040
Encyclopedic resources Wikidata; Q105508416
Entry history
Entry creation12-Jan-2021
Last entry update29-Jun-2023
Version number4