Cellosaurus cell line KOLF2.1J MAPT N279K SNV/WT (CVCL

Cellosaurus KOLF2.1J MAPT N279K SNV/WT (CVCL_E7R0)

[Text version]

Cell line name

KOLF2.1J MAPT N279K SNV/WT

Synonyms

JIPSC001788

Accession

CVCL_E7R0

Resource Identification Initiative

To cite this cell line use: KOLF2.1J MAPT N279K SNV/WT (RRID:CVCL_E7R0)

Comments

From: The Jackson Laboratory; Bar Harbor; USA.
Population: Caucasian; British.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.

Sequence variations

Mutation; HGNC; HGNC:18037; ARID2; Simple_corrected; p.Pro197Hisfs*12 (c.590_608delCTAAAATCATCACTTTACT); Zygosity=Heterozygous; Note=By CRISPR/Cas9 (from parent cell line).
Mutation; HGNC; HGNC:2201; COL3A1; Simple; c.3526-1G>A; Zygosity=Heterozygous; Note=Splice acceptor mutation (from parent cell line).
Mutation; HGNC; HGNC:2201; COL3A1; Simple; p.Gly1176Ser (c.3526G>A); Zygosity=Heterozygous (from parent cell line).
Mutation; HGNC; HGNC:6893; MAPT; Simple_edited; p.Asn279Lys (c.837T>G) (N596K, c.1788T>G or N614K, c.1842T>G); ClinVar=VCV000014253; Zygosity=Heterozygous; Note=By CRISPR/Cas9 (JAX).

Disease

Frontotemporal dementia (NCIt: C84719)
Parkinson disease (NCIt: C26845)
Behavioral variant of frontotemporal dementia (ORDO: Orphanet_275864)

Species of origin

Homo sapiens (Human) (NCBI Taxonomy: 9606)

Hierarchy

Parent: CVCL_B5P3 (KOLF2.1J)
Children:

CVCL_E7QY (KOLF2.1J MAPT N279K REV/WT)

Sex of cell

Male

Age at sampling

55-59Y