ID   RS4;11 mouse MCL1
AC   CVCL_E8JJ
SY   RS4;11-mouse-MCL1
DR   KYinno; KC-1346
CC   Population: Caucasian.
CC   Sequence variation: Gene fusion; HGNC; HGNC:7135; AFF1 + HGNC; HGNC:7132; KMT2A; Name(s)=KMT2A-AFF1, MLL-AFF1, ALL-1/AF4; Note=In frame (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:12766; NSD2; Simple; p.Glu1099Lys (c.3295G>A); ClinVar=VCV000638278; Zygosity=Heterozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; HGNC:8977; PIK3CD; Simple; p.Gly971Arg (c.2911G>A); ClinVar=VCV001337907; Zygosity=Heterozygous (from parent cell line).
CC   Genetic integration: Method=Transduction; Gene=MGI; MGI:101769; Mcl1.
CC   Genetic integration: Method=Transduction; Gene=UniProtKB; P13249; Streptomyces alboniger pac (PuroR).
CC   Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
DI   NCIt; C9143; Adult B acute lymphoblastic leukemia
DI   NCIt; C80342; B acute lymphoblastic leukemia with t(v;11q23.3) MLL rearranged
DI   ORDO; Orphanet_585918; B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0093 ! RS4;11
SX   Female
AG   32Y
CA   Cancer cell line
DT   Created: 14-08-25; Last updated: 14-08-25; Version: 1
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