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Cellosaurus NUIGi022-B (CVCL_XI98)

[Text version]
Cell line name NUIGi022-B
Synonyms ND11C7
Accession CVCL_XI98
Resource Identification Initiative To cite this cell line use: NUIGi022-B (RRID:CVCL_XI98)
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_WT08 ! NUIGi022-A
Sex of cell Male
Age at sampling 14Y
Category Induced pluripotent stem cell
Publications

PubMed=31759289; DOI=10.1016/j.scr.2019.101653
Yi-Cheng Ding, Berta Marco de la Cruz, Ya-Wen Xia, Min Liu, Yin Lu, Veronica McInerney, Janusz Krawczyk, Sally A. Lynch, Linda Howard, Timothy O'Brien, Louise Gallagher, San-Bing Shen;
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-B
Biological sample resources BioSamples; SAMEA6032107
Encyclopedic resources Wikidata; Q98128180
Entry history
Entry creation19-Dec-2019
Last entry update19-Dec-2024
Version number7