Cellosaurus cell line K10M19 (CVCL_T831)

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Cross-references
Cell line name	K10M19
Synonyms	K10-M19; HPS0105
Accession	CVCL_T831
Resource Identification Initiative	To cite this cell line use: K10M19 (RRID:CVCL_T831)
Comments	Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; 10288; RP9; Simple; p.His137Leu (c.410A>T); ClinVar=VCV000003334; Zygosity=Unspecified (PubMed=21347327).
Disease	Retinitis pigmentosa (NCIt: C85045) Retinitis pigmentosa (ORDO: Orphanet_791)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_T832 ! K10M5 CVCL_QX20 ! K10M15 CVCL_T830 ! K10M17
Sex of cell	Male
Age at sampling	39Y
Category	Induced pluripotent stem cell
Publications	PubMed=21347327; DOI=10.1371/journal.pone.0017084 Jin Z.-B., Okamoto S., Osakada F., Homma K., Assawachananont J., Hirami Y., Iwata T., Takahashi M. Modeling retinal degeneration using patient-specific induced pluripotent stem cells. PLoS ONE 6:E17084-E17084(2011)
Cell line collections (Providers)	RCB; HPS0105
Cell line databases/resources	SKIP; SKIP000136
Encyclopedic resources	Wikidata; Q54899243
Entry history
Entry creation	03-Feb-2014
Last entry update	29-Jun-2023
Version number	14