ID   H9/HTLV-IIIMN
AC   CVCL_X620
SY   H9/HTLV-IIIMN NIH 1984
DR   BEI_Resources; ARP-402
DR   cancercelllines; CVCL_X620
DR   Wikidata; Q54872248
CC   Population: Caucasian.
CC   Sequence variation: Gene deletion; HGNC; HGNC:7208; MPDZ; Zygosity=Homozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gln61Lys (c.181C>A); ClinVar=VCV000073058; Zygosity=Heterozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg196Ter (c.586C>T); ClinVar=VCV000043589; Zygosity=Homozygous (from parent cell line).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
CC   Cell type: T-cell; CL=CL_0000084.
DI   NCIt; C3366; Sezary syndrome
DI   ORDO; Orphanet_3162; Sezary syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_1240 ! H9
SX   Male
AG   53Y
CA   Cancer cell line
DT   Created: 05-09-14; Last updated: 19-12-24; Version: 16
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