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Cellosaurus NUIGi041-B (CVCL_YQ99)

[Text version]

Cell line name NUIGi041-B
Synonyms ND3C4
Accession CVCL_YQ99
Resource Identification Initiative To cite this cell line use: NUIGi041-B (RRID:CVCL_YQ99)
Comments From: National University of Ireland Galway; Galway; Ireland.
Population: Caucasian.
Derived from sampling site: Skin; dermis. Cell type=Fibroblast.
Sequence variations
  • Mutation; HGNC; 8008; NRXN1; Unexplicit; Ex1-5del; Zygosity=Heterozygous (PubMed=33578364).
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_YQ98 ! NUIGi041-A
Sex of cell Male
Age at sampling 20Y
Category Induced pluripotent stem cell
Publications

PubMed=33578364; DOI=10.1016/j.scr.2021.102222
Ding Y., O'Brien A., de la Cruz B.M., Yang M., Fitzgerald J., Yang G., Li W., McInerney V., Krawczyk J., Lynch S.A., Howard L., Allen N.M., O'Brien T., Gallagher L., Shen S.-B.
Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1alpha deletion (NUIGi041-A, NUIG041-B NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B).
Stem Cell Res. 52:102222-102222(2021)

Cross-references
Cell line databases/resources hPSCreg; NUIGi041-B
Biological sample resources BioSamples; SAMEA6465064
Encyclopedic resources Wikidata; Q98128212
Entry history
Entry creation12-Mar-2020
Last entry update16-Dec-2021
Version number4