Dataset | LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules |
Category | transcriptomics |
Type | small molecule perturbation |
Description | small molecule perturbation identified as [perturbation ID]_[perturbagen]_[cell line]_[time]_[time unit]_[dose]_[dose unit] (LINCS L1000 Connectivity Map) |
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59 genes differentially expressed following the BRD-A79768653_sirolimus_HT29_24_h_0.04_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
Symbol | Name |
---|---|
1060P11.3 | killer cell immunoglobulin-like receptor, three domains, pseudogene |
ALCAM | activated leukocyte cell adhesion molecule |
ARID4B | AT rich interactive domain 4B (RBP1-like) |
AZGP1 | alpha-2-glycoprotein 1, zinc-binding |
C14ORF159 | chromosome 14 open reading frame 159 |
CADPS2 | Ca++-dependent secretion activator 2 |
CLNS1A | chloride channel, nucleotide-sensitive, 1A |
EEF1A2 | eukaryotic translation elongation factor 1 alpha 2 |
EFNA1 | ephrin-A1 |
HOOK2 | hook microtubule-tethering protein 2 |
IFI27 | interferon, alpha-inducible protein 27 |
MAGED1 | melanoma antigen family D1 |
PDZK1IP1 | PDZK1 interacting protein 1 |
PRKACB | protein kinase, cAMP-dependent, catalytic, beta |
PRUNE2 | prune homolog 2 (Drosophila) |
RAB11FIP2 | RAB11 family interacting protein 2 (class I) |
RSRP1 | arginine/serine-rich protein 1 |
SEPP1 | selenoprotein P, plasma, 1 |
SLC35E2B | solute carrier family 35, member E2B |
SPARC | secreted protein, acidic, cysteine-rich (osteonectin) |
SPON2 | spondin 2, extracellular matrix protein |
SYNE2 | spectrin repeat containing, nuclear envelope 2 |
TCFL5 | transcription factor-like 5 (basic helix-loop-helix) |
TOX3 | TOX high mobility group box family member 3 |
TRIB2 | tribbles pseudokinase 2 |
VCAN | versican |
VPS13C | vacuolar protein sorting 13 homolog C (S. cerevisiae) |
Symbol | Name |
---|---|
ABCG2 | ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) |
AMMECR1 | Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 |
AQP3 | aquaporin 3 (Gill blood group) |
ATP8B1 | ATPase, aminophospholipid transporter, class I, type 8B, member 1 |
CD58 | CD58 molecule |
CDC42SE1 | CDC42 small effector 1 |
CEACAM1 | carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein) |
COL4A2 | collagen, type IV, alpha 2 |
CPM | carboxypeptidase M |
DDIT4 | DNA-damage-inducible transcript 4 |
EDEM1 | ER degradation enhancer, mannosidase alpha-like 1 |
EIF5A | eukaryotic translation initiation factor 5A |
ELN | elastin |
FGFR3 | fibroblast growth factor receptor 3 |
FOXD1 | forkhead box D1 |
GNL3L | guanine nucleotide binding protein-like 3 (nucleolar)-like |
GPM6A | glycoprotein M6A |
IL1RN | interleukin 1 receptor antagonist |
IL6R | interleukin 6 receptor |
KAT2B | K(lysine) acetyltransferase 2B |
MALL | mal, T-cell differentiation protein-like |
MARCKS | myristoylated alanine-rich protein kinase C substrate |
MEIS1 | Meis homeobox 1 |
MEIS2 | Meis homeobox 2 |
MLLT11 | myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 11 |
MUC4 | mucin 4, cell surface associated |
PPP1R13B | protein phosphatase 1, regulatory subunit 13B |
PRKAR2B | protein kinase, cAMP-dependent, regulatory, type II, beta |
PTGDS | prostaglandin D2 synthase 21kDa (brain) |
S100A2 | S100 calcium binding protein A2 |
SLC2A1 | solute carrier family 2 (facilitated glucose transporter), member 1 |
TM4SF1 | transmembrane 4 L six family member 1 |