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Cellosaurus KMUGMCi004-A (CVCL_C1LN)

[Text version]
Cell line name KMUGMCi004-A
Synonyms KMUGMCi004APC; KN615
Accession CVCL_C1LN
Resource Identification Initiative To cite this cell line use: KMUGMCi004-A (RRID:CVCL_C1LN)
Comments From: Kanazawa Medical University; Uchinada; Japan.
Population: Japanese.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 583; APC; Simple; p.Gly611Valfs*19 (c.1832delG); Zygosity=Heterozygous (PubMed=35868288).
Disease Familial adenomatous polyposis (NCIt: C3339)
Familial adenomatous polyposis (ORDO: Orphanet_733)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 39Y
Category Induced pluripotent stem cell

PubMed=35868288; DOI=10.1016/j.scr.2022.102867
Ura H., Togi S., Hatanaka H., Niida Y.
Establishment of a human induced pluripotent stem cell line, KMUGMCi004-A, from a patient bearing a heterozygous c.1832delG mutation in the APC gene leading familial adenomatous polyposis (FAP).
Stem Cell Res. 63:102867-102867(2022)

Cell line databases/resources hPSCreg; KMUGMCi004-A
Biological sample resources BioSamples; SAMEA110131367
Encyclopedic resources Wikidata; Q114311825
Entry history
Entry creation22-Sep-2022
Last entry update29-Jun-2023
Version number4