ID   ICC4
AC   CVCL_A1VI
DR   cancercelllines; CVCL_A1VI
DR   DepMap; ACH-001844
DR   Wikidata; Q105509603
CC   Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Leu137Gln (c.410T>A); Zygosity=Unspecified (DepMap=ACH-001844).
ST   Source(s): DepMap=ACH-001844
ST   Amelogenin: X,Y
ST   CSF1PO: 10,11
ST   D13S317: 10,11
ST   D16S539: 11,12
ST   D18S51: 12
ST   D21S11: 27,31.2
ST   D3S1358: 15
ST   D5S818: 11,13
ST   D7S820: 11,12
ST   D8S1179: 13,14
ST   FGA: 20,21
ST   Penta D: 10,11
ST   Penta E: 10,11
ST   TH01: 9,9.3
ST   TPOX: 8,11
ST   vWA: 18
DI   NCIt; C35417; Intrahepatic cholangiocarcinoma
DI   ORDO; Orphanet_70567; Cholangiocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
CA   Cancer cell line
DT   Created: 12-01-21; Last updated: 02-05-24; Version: 6
//