TRIM24


Summary: The protein encoded by this gene mediates transcriptional control by interaction with the activation function 2 (AF2) region of several nuclear receptors, including the estrogen, retinoic acid, and vitamin D3 receptors. The protein localizes to nuclear bodies and is thought to associate with chromatin and heterochromatin-associated factors. The protein is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains - a RING, a B-box type 1 and a B-box type 2 - and a coiled-coil region. Two alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location

Gene Categories:

TYROSINE KINASEKINASE

GO terms in TRIM24


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Term Type
Evidence Type
GO Term ID
GO Des.
CC IDA GO:0005634 nucleus
CC IDA GO:0005654 nucleoplasm
CC IEA GO:0005719 nuclear euchromatin
CC IEA GO:0005726 perichromatin fibrils
CC TAS GO:0005829 cytosol
BP TAS GO:0006366 transcription by RNA polymerase II
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Gene expression in normal tissue: TRIM24

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

undefined20PI3K/MTOR signaling2Biosynthesis of secondary metabolites1Metabolism1ERK MAPK signaling1One carbon pool by folate1Stilbenoid, diarylheptanoid and gingerol biosynthesis1Apoptosis regulation1

Pathways in TRIM24


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Database
Pathway ID
Pathway Des.
netpath Pathway_EGFR1 EGFR1
pid ar_tf_pathway Regulation of Androgen receptor activity
reactome R-HSA-1226099 Signaling by FGFR in disease
reactome R-HSA-1643685 Disease
reactome R-HSA-1839117 Signaling by cytosolic FGFR1 fusion mutants
reactome R-HSA-1839124 FGFR1 mutant receptor activation
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD202 Curcumin 2
iGMDRD474 Avrainvillamide 1
iGMDRD121 GMX1778 6
iGMDRD481 Dactolisib 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in TRIM24

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
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