ID A375.S2 AC CVCL_0136 SY A-375.S2; A375-S2; A375S2; A375s2 DR BTO; BTO_0005815 DR CLO; CLO_0001583 DR MCCL; MCC:0000029 DR ATCC; CRL-1872 DR BCRC; 60263 DR cancercelllines; CVCL_0136 DR GEO; GSM827493 DR LINCS_HMS; 50003 DR LINCS_LDP; LCL-1231 DR Progenetix; CVCL_0136 DR Wikidata; Q54606870 RX PubMed=20215515; CC Population: Caucasian. CC Sequence variation: Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Homozygous (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:1787; CDKN2A; Simple; p.Glu61Ter (c.181G>T) (p.Gly75Val, c.224G>T); ClinVar=VCV000376309; Zygosity=Homozygous (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:1787; CDKN2A; Simple; p.Glu69Ter (c.205G>T) (p.Gly83Val, c.248G>T); ClinVar=VCV000376308; Zygosity=Homozygous (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:11730; TERT; Simple; c.1-146C>T (c.250C>T) (C250T); Zygosity=Unspecified; Note=In promoter (from parent cell line). CC Omics: Variations; SNP array analysis. CC Miscellaneous: Not sure what is the relationship between A375.S2 and A375S1. CC Discontinued: ATCC; CRL-1872; true. CC Derived from site: In situ; Leg, skin; UBERON=UBERON_0001511. ST Source(s): ATCC=CRL-1872 ST Amelogenin: X ST CSF1PO: 11,12 ST D13S317: 11,14 ST D16S539: 9 ST D5S818: 12 ST D7S820: 9 ST TH01: 8 ST TPOX: 8,10 ST vWA: 16,17 DI NCIt; C3802; Amelanotic melanoma OX NCBI_TaxID=9606; ! Homo sapiens (Human) HI CVCL_0132 ! A-375 SX Female AG 54Y CA Cancer cell line DT Created: 04-04-12; Last updated: 10-04-25; Version: 29 // RX PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662; RA Rothenberg, S. Michael RA Mohapatra, Gayatry RA Rivera, Miguel N. RA Winokur, Daniel RA Greninger, Patricia RA Nitta, Mai RA Sadow, Peter M. RA Sooriyakumar, Gaya RA Brannigan, Brian W. RA Ulman, Matthew J. RA Perera, Rushika M. RA Wang, Rui RA Tam, Angela RA Ma, Xiao-Jun RA Erlander, Mark RA Sgroi, Dennis C. RA Rocco, James W. RA Lingen, Mark W. RA Cohen, Ezra E.W. RA Louis, David Neil RA Settleman, Jeffrey RA Haber, Daniel Arie RT "A genome-wide screen for microdeletions reveals disruption of RT polarity complex genes in diverse human cancers."; RL Cancer Res. 70:2158-2164(2010). //