Target intelligence / Profile preview

Chromosome 3 open reading frame 33 (C3orf33)

Target
C3orf33
Molecular classification
Other (Secreted protein; not classified as receptor, enzyme, transporter, or transcription factor based on available data)[4][2][11], Negative regulator of ERK1/ERK2 signaling[2][3][4][11]
01

Overview

Chromosome 3 open reading frame 33 (C3orf33) encodes a protein that is primarily secreted and thought to participate in transcription regulation, notably through inhibition of the ERK1/ERK2 signaling cascade via an as-yet unidentified receptor on the plasma membrane[2][3][4][11]. The protein is annotated as having some nucleic acid binding and potential hydrolase activity on ester bonds[2], but remains poorly characterized at the molecular level and is not categorized within major receptor, enzyme, transporter, or ion channel families. Its expression is notable in the extracellular space[2][3][4][11], and gene variants are associated with familial temporal lobe epilepsy as well as frontotemporal dementia/ALS, suggesting a possible role in certain neurodegenerative conditions[2]. No drugs currently target C3orf33, and its mechanism of action in disease or therapy remains to be elucidated[2][3][4][11].

Other names
C3orf33AC3-33FLJ31139MSTP052Protein C3orf33Protein AC3-33C3orf33lAP-1 activity suppressorC2h3orf33E130311K13RikRGD1565059RIKEN cDNA E130311K13 gene
02

Mechanism of action

Not established. No drugs known to act on C3orf33 or exploit its function/pathway for therapeutic benefit.[2][3][4][11]

03

Biological functions

Regulation of DNA-binding transcription factor activity[2][3][11]Negative regulation of ERK1 and ERK2 cascade[2][3][4][11]May play a role in transcription regulation via MAPK3/MAPK1 (ERK1/2) signaling pathway[11]Secreted protein with unidentified receptor interaction[4][11]
04

Disease associations

Epilepsy, familial temporal lobe, 3[2]Frontotemporal dementia and/or amyotrophic lateral sclerosis 7[2]Other (potential links to neurodegenerative disease suggested by association with frontotemporal dementia/ALS)[2]
05

Safety considerations

Not reported. There are no notable safety concerns or therapeutic challenges documented for targeting C3orf33.[2][3][4][11]
06

Interacting drugs

None reported. There are currently no drugs identified as interacting with C3orf33 in public databases.[2][3][4][11]
07

Biomarkers

None reported. No established use as a biomarker for patient selection or efficacy monitoring.[2][3][4][11]

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