Cellosaurus cell line WAe009-A-82 (CVCL

Cross-references
Cell line name	WAe009-A-82
Synonyms	SMUDHe010-A-82
Accession	CVCL_B5QN
Resource Identification Initiative	To cite this cell line use: WAe009-A-82 (RRID:CVCL_B5QN)
Comments	From: Southern Medical University; Guangzhou; China. Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358. Cell type: Embryonic stem cell; CL=CL_0002322.
Sequence variations	Mutation; HGNC; 8507; OSMR; Simple_edited; p.Gly513Asp (c.1538G>A); ClinVar=VCV000802119; Zygosity=Homozygous; Note=By CRISPR/Cas9 (PubMed=35714449).
Disease	Familial primary localized cutaneous amyloidosis-1 (NCIt: C189282) Familial primary localized cutaneous amyloidosis (ORDO: Orphanet_353220)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy	Parent: CVCL_9773 (WA09)
Sex of cell	Female
Age at sampling	Blastocyst stage
Category	Embryonic stem cell
Publications	PubMed=35714449; DOI=10.1016/j.scr.2022.102842 Zheng W., Zhong Y.-D., Yuan L.-Y., Yu X.-L., Wang X., Yang C., Liu H.-T., Lv P., Luo Y.-Y., Qiu B.-Y., Liu J., Yang B. Generation of a human embryonic stem cell line (SMUDHe010-A-82) carrying a homozygous c.1538G > A (p.G513D) mutation in the OSMR gene by CRISPR/Cas9-mediated homologous recombination. Stem Cell Res. 63:102842-102842(2022)
Cell line databases/resources	hPSCreg; WAe009-A-82
Biological sample resources	BioSamples; SAMEA12121387
Encyclopedic resources	Wikidata; Q112041926
Entry history
Entry creation	17-Mar-2022
Last entry update	29-Jun-2023
Version number	5