Cellosaurus cell line TD-15 (CVCL

Cellosaurus TD-15 (CVCL_E6KV)

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Cell line name

TD-15

Accession

CVCL_E6KV

Resource Identification Initiative

To cite this cell line use: TD-15 (RRID:CVCL_E6KV)

Comments

From: Clinical Biospecimen Imaging and Genetic (C-BIG) Repository, Montreal Neurological Institute, McGill University; Montreal; Canada.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.

Sequence variations

Mutation; HGNC; HGNC:11179; SOD1; Simple; p.Ile114Thr (c.341T>C) (I113T); ClinVar=VCV000197145; Zygosity=Heterozygous (PubMed=34500068).

Disease

Amyotrophic lateral sclerosis 1 (NCIt: C168749)
Amyotrophic lateral sclerosis (ORDO: Orphanet_803)

Species of origin

Homo sapiens (Human) (NCBI Taxonomy: 9606)

Hierarchy

Children:

CVCL_E6KW (TD-15 corrected clone H02)

Sex of cell

Female

Age at sampling

45Y

Category

Induced pluripotent stem cell

STR profile

Source(s): PubMed=34500068

Markers:

Amelogenin	X
CSF1PO	12,13
D5S818	12,13
D7S820	9,11
D13S317	11
D16S539	9,12
D21S11	28,31.2
TH01	7,8
TPOX	11
vWA	16,17

Web pages

Provider; C-BIG; -; https://cbigr-open.loris.ca/C-BIG_ipsc_catalog_august_2023.pdf

Publications

PubMed=34500068; DOI=10.1016/j.ymeth.2021.09.002
Eric Deneault, Mathilde Chaineau, Michael Nicouleau, Maria Jose Castellanos-Montiel, Anna Kristyna Franco-Flores, Ghazal Haghi, Carol Xiu-Qing Chen, Narges Abdian, Irina Shlaifer, Lenore K. Beitel, Thomas M. Durcan;
A streamlined CRISPR workflow to introduce mutations and generate isogenic iPSCs for modeling amyotrophic lateral sclerosis.
Methods 203:297-310(2022)

Entry history

Entry creation

10-Apr-2025

Last entry update

10-Apr-2025

Version number