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Cellosaurus CCD2-iPS 4 (CVCL_A4TK)

[Text version]
Cell line name CCD2-iPS 4
Accession CVCL_A4TK
Resource Identification Initiative To cite this cell line use: CCD2-iPS 4 (RRID:CVCL_A4TK)
Comments From: Department of Biochemistry, Tokyo Dental College; Tokyo; Japan.
Derived from site: In situ; Oral cavity, oral mucosa; UBERON=UBERON_0003729.
Sequence variations
  • Mutation; HGNC; HGNC:10472; RUNX2; Simple; p.Gln67Ter (c.199C>T); Zygosity=Heterozygous (PubMed=29357927).
Disease Cleidocranial dysplasia (NCIt: C75020)
Cleidocranial dysplasia (ORDO: Orphanet_1452)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_A4TL ! CCD2-iPS 7
CVCL_A4TM ! CCD2-iPS 8
CVCL_A4TN ! CCD2-iPS 9
CVCL_A4TP ! CCD2-iPS 12
Sex of cell Female
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Publications

PubMed=29357927; DOI=10.1186/s13287-017-0754-4; PMCID=PMC5778688
Akiko Saito, Akio Ooki, Takashi Nakamura, Shoko Onodera, Kamichika Hayashi, Daigo Hasegawa, Takahito Okudaira, Katsuhito Watanabe, Hiroshi Kato, Takeshi Onda, Akira Watanabe ...Show all 19 authors... , Kenjiro Kosaki, Ken Nishimura, Manami Ohtaka, Mahito Nakanishi, Teruo Sakamoto, Akira Yamaguchi, Kenji Sueishi, Toshifumi Azuma; Show fewer authors
Targeted reversion of induced pluripotent stem cells from patients with human cleidocranial dysplasia improves bone regeneration in a rat calvarial bone defect model.
Stem Cell Res. Ther. 9:12.1-12.10(2018)

Cross-references
Cell line databases/resources SKIP; SKIP003021
Encyclopedic resources Wikidata; Q107114617
Entry history
Entry creation20-May-2021
Last entry update19-Dec-2024
Version number5