2 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
βGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
14PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITYβ Experimental GO Evidenceβ Swiss-Prot Reviewed
protein bindingregulation of inflammatory responsemembraneTORC2 complex bindingAbruptio Placentaesmoking initiationdiabetes mellitusAbnormality of the gastrointestinal tract
Based on limited published evidence, ARMH4 is a membrane-associated protein with potential roles in immune modulation and cell signaling. It down-modulates STAT3 signaling through direct interaction with IL6ST, inhibiting STAT3 phosphorylation at Tyr-705 1. ARMH4 may negatively regulate AKT signaling by modulating mTORC2 activity through RICTOR interaction. In podocytes, ARMH4 overexpression reduces inflammatory mediator release (IL-1B and IL-8), while silencing increases their release 2. The protein is downregulated in glomerular pathologies, suggesting a protective role in kidney disease. ARMH4 has also been identified as a transcriptomic biomarker in oral cancer margins 3.
1
ARMH4 down-modulates STAT3 signaling through IL6ST interaction, inhibiting STAT3 Tyr-705 phosphorylation
PMID: 269276692
ARMH4 overexpression reduces inflammatory mediator release (IL-1B, IL-8) in kidney epithelial cells; downregulated in glomerular pathologies
PMID: 366492293
ARMH4 identified as transcriptomic biomarker for discrimination of oral cancer surgical margins
PMID: 35327656β Limited data available β This gene has 3 indexed publications. Summary and analysis may be incomplete.
Abruptio PlacentaeOpen Targets
smoking initiationOpen Targets
diabetes mellitusOpen Targets
Abnormality of the gastrointestinal tractOpen Targets
Ichthyosis - hepatosplenomegaly - cerebellar degenerationOpen Targets
ichthyosis-hepatosplenomegaly-cerebellar degeneration syndromeOpen Targets
Benign familial choreaOpen Targets
familial hemolytic anemiaOpen Targets
urethral syndromeOpen Targets
glycoprotein storage diseaseOpen Targets
hemoglobin H diseaseOpen Targets
systemic lupus erythematosusOpen Targets
Hemoglobin C - beta-thalassemiaOpen Targets
hemoglobin C-beta-thalassemia syndromeOpen Targets
dominant beta-thalassemiaOpen Targets
combined immunodeficiency due to OX40 deficiencyOpen Targets
ovarian dysfunctionOpen Targets
ulcerative colitisOpen Targets
trauma complicationOpen Targets
No pathogenic variants reported on ClinVar for this gene.