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Cellosaurus NUIGi023-B (CVCL_XI92)

[Text version]
Cell line name NUIGi023-B
Synonyms ND12C2
Accession CVCL_XI92
Resource Identification Initiative To cite this cell line use: NUIGi023-B (RRID:CVCL_XI92)
Comments From: National University of Ireland Galway; Galway; Ireland.
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:8008; NRXN1; Unexplicit; Ex1-5del; Zygosity=Heterozygous (PubMed=31759289).
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_WU49 ! NUIGi023-A
Sex of cell Female
Age at sampling 15Y
Category Induced pluripotent stem cell
Publications

PubMed=31759289; DOI=10.1016/j.scr.2019.101653
Ding Y.-C., de la Cruz B.M., Xia Y.-W., Liu M., Lu Y., McInerney V., Krawczyk J., Lynch S.A., Howard L., O'Brien T., Gallagher L., Shen S.-B.
Derivation of familial iPSC lines from three ASD patients carrying NRXN1alpha(+/-) and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B NUIGi026-A, NUIGi026-B).
Stem Cell Res. 41:101653-101653(2019)

Cross-references
Cell line databases/resources hPSCreg; NUIGi023-B
Biological sample resources BioSamples; SAMEA6032110
Encyclopedic resources Wikidata; Q98128183
Entry history
Entry creation19-Dec-2019
Last entry update19-Dec-2024
Version number7