Cellosaurus cell line XXMUFAi001-A (CVCL

Cross-references
Cell line name	XXMUFAi001-A
Accession	CVCL_E8YH
Resource Identification Initiative	To cite this cell line use: XXMUFAi001-A (RRID:CVCL_E8YH)
Comments	From: The First Affiliated Hospital of Xinxiang Medical University; Xinxiang; China. Population: Chinese; Han. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations	Mutation; HGNC; HGNC:6251; KCNH2; Simple; p.Lys897Thr (c.2690A>C); ClinVar=VCV000067427; Zygosity=Heterozygous (PubMed=39709756).
Disease	Long QT syndrome 2 (NCIt: C137957) Romano-Ward syndrome (ORDO: Orphanet_101016)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	15Y
Category	Induced pluripotent stem cell
Publications	PubMed=39709756; DOI=10.1016/j.scr.2024.103635 Xiao-Lei Li, Jun-Biao Zhang, Xiao-Feng Wang, Da-Wei Pu, Zhen-Ling Zhang, Yi-Fang Niu, Shuai Zhang, Zhen-Ping Fan, Yu-Xuan Li, Pei-Cheng Li, Hui Liu ...Show all 14 authors... , Feng-Hua Lv, Yong-Chun Zhang, Ya-Nan Li; Show fewer authors Human induced pluripotent stem cell line XXMUFAi001-A generated from a patient harboring KCNH2 mutation (c.2690 A>C). Stem Cell Res. 82:103635-103635(2025)
Cell line databases/resources	hPSCreg; XXMUFAi001-A
Biological sample resources	BioSamples; SAMEA115758137
Entry history
Entry creation	14-Aug-2025
Last entry update	14-Aug-2025
Version number	1