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Cellosaurus NUIGi022-A (CVCL_WT08)

[Text version]

Cell line name NUIGi022-A
Synonyms ND11C2
Accession CVCL_WT08
Resource Identification Initiative To cite this cell line use: NUIGi022-A (RRID:CVCL_WT08)
Comments From: National University of Ireland Galway; Galway; Ireland.
Population: Caucasian.
Derived from sampling site: Skin.
Sequence variations Heterozygous for NRXN1 Ex1-5del (PubMed=31759289).
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_XI98 ! NUIGi022-B
Sex of cell Male
Age at sampling 14Y
Category Induced pluripotent stem cell
Publications

PubMed=31759289; DOI=10.1016/j.scr.2019.101653
Ding Y.-C., Marco de la Cruz B., 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; NUIGi022-A
Biological sample resources BioSamples; SAMEA5780091
Other Wikidata; Q98128178
Entry history
Entry creation05-Jul-2019
Last entry update29-Oct-2020
Version number4