Target intelligence / Profile preview

DnaJ heat shock protein family (Hsp40) member C27 (DNAJC27)

Target
DNAJC27
Molecular classification
Heat shock protein (Hsp40/DnaJ family), GTPase, Chaperone-associated protein
01

Overview

DnaJ heat shock protein family (Hsp40) member C27 (DNAJC27) is a member of the Hsp40/DnaJ co-chaperone families, predicted to function as a small Ras-like GTPase. It is involved in intracellular protein transport and is located in the cytoplasm, cytoplasmic vesicles, and nucleus[1][2][6][7]. DNAJC27 has been shown to activate the MEK/ERK pathway, potentially by serving as a nuclear scaffold for MAPK1/ERK2, thus enhancing ERK signaling and influencing cell transformation when overexpressed[2][3]. Genome-wide association studies indicate that variants in or near DNAJC27 are linked to variation in human body mass index, supporting a role in energy metabolism and obesity susceptibility[1]. Elevated circulating DNAJC27 is seen in obese individuals and patients with type 2 diabetes, suggesting a possible contributory role in these metabolic diseases[1]. There is no current evidence that DNAJC27 is a direct therapeutic target or druggable protein, but its function at the interface of stress response and metabolism makes it of interest for further research into metabolic and stress-related diseases[1][2][6].

Other names
RBJRABJSRabJSRab and DnaJ domain-containing proteinDnaJ homolog subfamily C member 27
02

Biological functions

Intracellular protein transportStress response modulationRegulation of energy metabolismScaffold protein for MAPK1 (supports ERK pathway activation)Maintenance of protein homeostasis under metabolic stress
03

Disease associations

Obesity (susceptibility and metabolic dysregulation)Type 2 diabetes (associated metabolic disorder)Eyelid benign neoplasm (reported disease association in database)Potential broader roles in cellular stress-related disorders
04

Biomarkers

Circulating/plasma DNAJC27 levels (reported as elevated in obesity and type 2 diabetes; may be explored as a metabolic biomarker)

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