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Cellosaurus PDSH723R01#16 (CVCL_RL26)

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Cell line name PDSH723R01#16
Synonyms H723R clone #16; H723R #16
Accession CVCL_RL26
Resource Identification Initiative To cite this cell line use: PDSH723R01#16 (RRID:CVCL_RL26)
Comments Population: Japanese.
Omics: Genomics; Whole exome sequencing.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
Disease Pendred syndrome (NCIt: C121745)
Pendred syndrome (ORDO: Orphanet_705)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_RL33 (GE#21)CVCL_RL34 (GE#22)CVCL_RL35 (GE#24)
CVCL_RL36 (GE#51)CVCL_RL37 (GE#81)CVCL_RL38 (GE#83)
CVCL_RL39 (GE#91)
Originate from same individual CVCL_RL24 ! PDSH723R01#5
CVCL_RL25 ! PDSH723R01#12
Sex of cell Female
Age at sampling 7Y
Category Induced pluripotent stem cell
Publications

PubMed=28052261; DOI=10.1016/j.celrep.2016.12.020
Makoto Hosoya, Masato Fujioka, Takefumi Sone, Satoshi Okamoto, Wado Akamatsu, Hideki Ukai, Hiroki R. Ueda, Kaoru Ogawa, Tatsuo Matsunaga, Hideyuki Okano;
Cochlear cell modeling using disease-specific iPSCs unveils a degenerative phenotype and suggests treatments for congenital progressive hearing loss.
Cell Rep. 18:68-81(2017)

Cross-references
Cell line databases/resources SKIP; SKIP001746
Encyclopedic resources Wikidata; Q54946854
Entry history
Entry creation05-Mar-2018
Last entry update10-Apr-2025
Version number10