Cell line name |
Jurkat D1.1 |
Synonyms |
D1.1; D1-1 |
Accession |
CVCL_3502 |
Resource Identification Initiative |
To cite this cell line use: Jurkat D1.1 (RRID:CVCL_3502) |
Comments |
Group: Patented cell line. Registration: International Depositary Authority, American Type Culture Collection (ATCC); CRL-10915. Population: Caucasian. Characteristics: CD4 negative subclone of Jurkat. Induces B cells to express surfac CD 23 molecules, a marker of B cell activation and to proliferate and terminally differentiate into Ig-secreting cells in the presence of T cell dependent B cell mitogens (PubMed=1834738). Omics: SNP array analysis. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. Cell type: T-cell; CL=CL_0000084. |
Sequence variations |
- Mutation; HGNC; HGNC:959; BAX; Simple; p.Glu41Argfs*19 (c.121delG); ClinVar=VCV000009512; Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:959; BAX; Simple; p.Glu41Glyfs*33 (c.121dupG); ClinVar=VCV000009511; Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg505Cys (c.1513C>T); ClinVar=VCV000069961; Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:6079; INPP5D; Simple; p.Gln345Ter (c.1033C>T); Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:6079; INPP5D; Simple; c.1097+1065_1097+1112del47; Zygosity=Heterozygous (from parent cell line).
- Mutation; HGNC; HGNC:7325; MSH2; Simple; p.Arg711Ter (c.2131C>T); ClinVar=VCV000090903; Zygosity=Homozygous (from parent cell line).
- Mutation; HGNC; HGNC:7329; MSH6; Simple; p.Phe1088Serfs*2 (c.3261delC); ClinVar=VCV000089363; Zygosity=Homozygous (from parent cell line).
- Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg196Ter (c.586C>T); ClinVar=VCV000043589; Zygosity=Heterozygous (from parent cell line).
|
Disease |
Childhood T acute lymphoblastic leukemia (NCIt: C7953) Precursor T-cell acute lymphoblastic leukemia (ORDO: Orphanet_99861) |
Species of origin |
Homo sapiens (Human)
(NCBI Taxonomy: 9606) |
Hierarchy |
Parent: CVCL_0065 (Jurkat) |
Sex of cell |
Male |
Age at sampling |
14Y |
Category |
Cancer cell line |
STR profile |
Source(s): ATCC=CRL-3600
Markers:Amelogenin | X |
CSF1PO | 11,12 |
D2S1338 | 19,23 |
D3S1358 | 13,15,16,17 |
D5S818 | 9 |
D7S820 | 8,10 |
D8S1179 | 12,13 |
D13S317 | 8,11 |
D16S539 | 10,11 |
D18S51 | 12,13,20,21 |
D19S433 | 13,14.2,15.2 |
D21S11 | 31.2,32.2,33.2,34.2 |
FGA | 19,20,21 |
Penta D | 11,13 |
Penta E | 10,12 |
TH01 | 6,9.3 |
TPOX | 8,10 |
vWA | 18,19,20 |
Run an STR similarity search on this cell line |
Web pages |
http://www.cells-talk.com/index.php/page/copelibrary?key=D1.1 |
Publications | PubMed=1834738; DOI=10.4049/jimmunol.147.10.3389 Yellin M.J., Lee J.J., Chess L., Lederman S. A human CD4- T cell leukemia subclone with contact-dependent helper function. J. Immunol. 147:3389-3395(1991) Patent=US6331433 Lederman S., Chess L., Yellin M.J. Human T cell leukemia cell line designated D1.1. Patent number US6331433, 18-Dec-2001 PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662 Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A. A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers. Cancer Res. 70:2158-2164(2010) |
Cross-references |
Cell line collections (Providers) |
ATCC; CRL-3600
ATCC; CRL-10915 - Discontinued
|
Cell line databases/resources |
CLO; CLO_0002658
cancercelllines; CVCL_3502
|
Biological sample resources |
BioSample; SAMN03471307
|
Encyclopedic resources |
Wikidata; Q54899131
|
Gene expression databases |
GEO; GSM827149
|
Polymorphism and mutation databases |
Cosmic; 683659
Progenetix; CVCL_3502
|
Entry history |
Entry creation | 04-Apr-2012 |
Last entry update | 19-Dec-2024 |
Version number | 28 |
---|