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Cellosaurus HPS1776 (CVCL_UN90)

Cell line name HPS1776
Accession CVCL_UN90
Resource Identification Initiative To cite this cell line use: HPS1776 (RRID:CVCL_UN90)
Comments Population: Japanese.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 7459; MT-ND4; Simple; p.Arg340His (m.11778G>A); ClinVar=VCV000009708; Zygosity=Unspecified (RCB=HPS1776).
Disease Leber hereditary optic atrophy (NCIt: C84808)
Leber hereditary optic neuropathy (ORDO: Orphanet_104)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 20-29Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS1776
Encyclopedic resources Wikidata; Q94219838
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number7