ID   Hs 738.St/Int
AC   CVCL_0880
DR   CLO; CLO_0004085
DR   ATCC; CRL-7869
DR   GEO; GSM827263
DR   Wikidata; Q54895965
RX   PubMed=20215515;
CC   Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982).
CC   Population: Caucasian.
CC   Omics: SNP array analysis.
CC   Derived from site: In situ; Fetal intestine; UBERON=UBERON_0000160.
CC   Derived from site: In situ; Fetal stomach; UBERON=UBERON_0000945.
CC   Cell type: Fibroblast; CL=CL_0000057.
ST   Source(s): ATCC=CRL-7869
ST   Amelogenin: X,Y
ST   CSF1PO: 10,11
ST   D13S317: 8,11
ST   D16S539: 9,11
ST   D18S51: 17,22
ST   D19S433: 13,14
ST   D21S11: 29,32.2
ST   D2S1338: 17
ST   D3S1358: 16,17
ST   D5S818: 11,13
ST   D7S820: 8,12
ST   D8S1179: 10,13
ST   FGA: 21,25
ST   Penta D: 9,10
ST   Penta E: 11,15
ST   TH01: 7,9.3
ST   TPOX: 8
ST   vWA: 16,18
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_T279 ! FHs 738Bl
OI   CVCL_3309 ! FHs 738Lu
OI   CVCL_R767 ! Hs 738.Bl
OI   CVCL_S035 ! Hs 738.Eye
OI   CVCL_S314 ! Hs 738.K/Ad/Ts
OI   CVCL_0879 ! Hs 738.Lu
SX   Male
AG   18FW
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 02-05-24; Version: 12
//
RX   PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458;
RA   Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P.,
RA   Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J.,
RA   Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C.,
RA   Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J.,
RA   Haber D.A.;
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).
//