ID   M8166
AC   CVCL_1H07
DR   HIVReagentProgram; ARP-11395
DR   Wikidata; Q54903650
RX   PubMed=32938764;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 7989; NRAS; Simple; p.Gln61Lys (c.181C>A); ClinVar=VCV000073058; Zygosity=Heterozygous (from parent cell line).
CC   Transformant: NCBI_TaxID; 11908; Human T-lymphotropic virus 1 (HTLV-1).
CC   Derived from site: In situ; Umbilical cord blood; UBERON=UBERON_0012168.
ST   Source(s): PubMed=32938764
ST   Amelogenin: X,Y
ST   CSF1PO: 10
ST   D13S317: 10,11
ST   D16S539: 12,13
ST   D18S51: 14,17
ST   D21S11: 27,30
ST   D3S1358: 15,16
ST   D5S818: 12
ST   D7S820: 9,10
ST   D8S1179: 11,14
ST   FGA: 21,22
ST   Penta D: 11,15
ST   Penta E: 7,11
ST   TH01: 6,9.3
ST   TPOX: 11
ST   vWA: 15,16
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_1099 ! C8166
SX   Male
AG   <1D
CA   Transformed cell line
DT   Created: 08-07-15; Last updated: 29-06-23; Version: 12
//
RX   PubMed=32938764; DOI=10.1128/JVI.01334-20;
RA   Fernandez M.V., Hoffman H.K., Pezeshkian N., Tedbury P.R.,
RA   van Engelenburg S.B., Freed E.O.;
RT   "Elucidating the basis for permissivity of the MT-4 T-cell line to
RT   replication of an HIV-1 mutant lacking the gp41 cytoplasmic tail.";
RL   J. Virol. 94:e01334.20.1-e01334.20.27(2020).
//