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Cellosaurus Dch4F (CVCL_F012)

Cell line name Dch4F
Accession CVCL_F012
Resource Identification Initiative To cite this cell line use: Dch4F (RRID:CVCL_F012)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Dyschromatosis symmetrica hereditaria (NCIt: C118435)
Dyschromatosis symmetrica hereditaria (ORDO: Orphanet_41)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 34Y
Category Finite cell line
STR profile Source(s): JCRB

Markers:
AmelogeninX,Y
CSF1PO11,12
D5S81811,12
D7S8208,11
D13S3178,10
D16S5399,10
TH016
TPOX9,11
vWA14,18

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Cross-references
Cell line collections (Providers) JCRB; JCRB3004
JCRB; KURB2101 - Discontinued
Biological sample resources BioSample; SAMN03472404
Encyclopedic resources Wikidata; Q54828677
Entry history
Entry creation22-Oct-2012
Last entry update29-Jun-2023
Version number13