Cellosaurus cell line MNDINSi001-A (CVCL

Cross-references
Cell line name	MNDINSi001-A
Synonyms	hiPSC-ins8
Accession	CVCL_A9YK
Resource Identification Initiative	To cite this cell line use: MNDINSi001-A (RRID:CVCL_A9YK)
Comments	From: Endocrinology Research Centre; Moscow; Russia. Population: Caucasian. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:6081; INS; Simple; c.188-31G>A; ClinVar=VCV000211186; Zygosity=Heterozygous (PubMed=32739878).
Disease	Permanent neonatal diabetes mellitus (NCIt: C114902) Permanent neonatal diabetes mellitus (ORDO: Orphanet_99885)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Female
Age at sampling	3Y
Category	Induced pluripotent stem cell
Publications	PubMed=32739878; DOI=10.1016/j.scr.2020.101929 Panova A.V., Klementieva N.V., Sycheva A.V., Goliusova D.V., Khokhlov N.V., Zubkova N.A., Tiulpakov A.N., Kiselev S.L. Generation of an induced pluripotent stem cell line MNDINSi001-A from a patient with neonatal diabetes caused by a heterozygous INS mutation. Stem Cell Res. 47:101929-101929(2020)
Encyclopedic resources	Wikidata; Q102114546
Entry history
Entry creation	29-Oct-2020
Last entry update	19-Dec-2024
Version number	7