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Cellosaurus CHIpMSC1 (CVCL_B3MQ)

[Text version]
Cell line name CHIpMSC1
Synonyms F-CHI
Accession CVCL_B3MQ
Resource Identification Initiative To cite this cell line use: CHIpMSC1 (RRID:CVCL_B3MQ)
Comments Derived from site: In situ; Pancreas; UBERON=UBERON_0001264.
Cell type: Mesenchymal stem cell; CL=CL_0000134.
Sequence variations
Disease Persistent hyperinsulinemic hypoglycemia of infancy (NCIt: C122923)
Autosomal dominant hyperinsulinism due to SUR1 deficiency (ORDO: Orphanet_276575)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 4M
Category Somatic stem cell
STR profile Source(s): CelloPub=CLPUB00652

Markers:
AmelogeninX,Y
CSF1PO11,13
D3S135814,18
D5S81811,12
D7S82011
D8S117913,15
D13S3178,12
D16S53912
D18S5112
D21S1127,29
FGA19,21
Penta D9,12
Penta E7,12
TH017,9.3
TPOX10,11
vWA14

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Publications

CLPUB00652
Kellaway S.G.
Stem cells from patients with congenital hyperinsulinism.
Thesis PhD (2016); University of Manchester; Manchester; United Kingdom

PubMed=31525223; DOI=10.1371/journal.pone.0222350; PMCID=PMC6746350
Kellaway S.G., Mosinska K., Mohamed Z., Ryan A., Richardson S.M., Newbould M., Banerjee I., Dunne M.J., Cosgrove K.E.
Increased proliferation and altered cell cycle regulation in pancreatic stem cells derived from patients with congenital hyperinsulinism.
PLoS ONE 14:E0222350-E0222350(2019)

Cross-references
Encyclopedic resources Wikidata; Q110432706
Entry history
Entry creation16-Dec-2021
Last entry update19-Dec-2024
Version number6