Target intelligence / Profile preview

Zinc finger protein 225 (ZNF225)

Target
ZNF225
Molecular classification
Transcription factor, C2H2-type zinc finger protein
01

Overview

Zinc finger protein 225 (ZNF225) is a human protein encoded by the ZNF225 gene and is classified as a C2H2-type zinc finger transcription factor[3][4][5][1]. It is predicted to function primarily in the regulation of transcription as a DNA-binding transcriptional activator or repressor, specifically for genes transcribed by RNA polymerase II[1][3][6]. ZNF225 is part of a large family of zinc finger proteins that act as key regulators of gene expression, influencing a range of cellular processes[2][3]. While ZNF225 has no established function as a drug target, it has been identified as part of multi-gene prognostic models in cancers such as esophageal carcinoma, where its expression correlates with patient risk and prognosis[2]. There is limited direct functional characterization in disease beyond these correlative cancer studies, and no drugs or therapies currently target ZNF225 directly[2].

Other names
ZNF225Zinc finger protein 225
02

Mechanism of action

Not applicable (no direct targeting drugs identified)

03

Biological functions

Regulation of transcription by RNA polymerase IIDNA bindingRNA polymerase II cis-regulatory region sequence-specific DNA binding activity
04

Disease associations

Cancer (notably implicated as a prognostic marker/gene signature in cancers such as esophageal carcinoma and suggested in hepatocellular carcinoma)Other (broad role in gene regulation with potential implications in diverse pathologies via altered transcriptional regulation, but no established direct disease causality beyond cancer-related associations)
05

Safety considerations

Not established (no evidence of safety concerns or therapeutic challenges specifically related to ZNF225 modulation; it is not an established direct therapeutic target)
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Interacting drugs

None known
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Biomarkers

Prognostic marker for esophageal carcinoma (in gene signature models identifying risk/prognostic subgroups)

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