Cellosaurus cell line PDSHT410M#11 (CVCL

Cross-references
Cell line name	PDSHT410M#11
Synonyms	T410M clone #11
Accession	CVCL_RL31
Resource Identification Initiative	To cite this cell line use: PDSHT410M#11 (RRID:CVCL_RL31)
Comments	Population: Japanese. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations	Mutation; HGNC; HGNC:8818; SLC26A4; Simple; p.Thr410Met (c.1229C>T); ClinVar=VCV000043498; Zygosity=Homozygous (PubMed=28052261).
Disease	Pendred syndrome (NCIt: C121745) Pendred syndrome (ORDO: Orphanet_705)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_RL30 ! PDSHT410M#3 CVCL_RL32 ! PDSHT410M#12
Sex of cell	Female
Age at sampling	4Y
Category	Induced pluripotent stem cell
Publications	PubMed=28052261; DOI=10.1016/j.celrep.2016.12.020 Hosoya M., Fujioka M., Sone T., Okamoto S., Akamatsu W., Ukai H., Ueda H.R., Ogawa K., Matsunaga T., Okano H. 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)
Cell line databases/resources	SKIP; SKIP001753
Encyclopedic resources	Wikidata; Q54946864
Entry history
Entry creation	05-Mar-2018
Last entry update	19-Dec-2024
Version number	9