1 sources retrieved · Most recent: April 2026 · Index updated 16 days ago
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40PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingsmall GTPase bindingCCR4-NOT complex bindingRac protein signal transductionAbnormality of the skeletal systemalcohol drinkingintestinal obstructionattention deficit hyperactivity disorder
Based on limited published evidence, GARRE1 acts as an effector of RAC1 in small GTPase signaling 1. It associates with the CCR4-NOT complex, a major cellular mRNA deadenylase involved in bulk mRNA degradation, miRNA-mediated repression, and translational regulation 2. GARRE1 may participate in miRNA silencing machinery 2. Recent RNA-seq analysis suggests GARRE1 expression in pubertal mammary epithelial cells may provide protective effects for immune and DNA damage responses 3.
2
GARRE1 associates with CCR4-NOT complex involved in mRNA degradation, miRNA-mediated repression, and translational regulation; may play a role in miRNA silencing
PMID: 293950673
GARRE1 expression in pubertal mammary epithelial cells may provide protective effects for immune and DNA damage responses
PMID: 39599711⚠Limited data available — This gene has 3 indexed publications. Summary and analysis may be incomplete.
Abnormality of the skeletal systemOpen Targets
alcohol drinkingOpen Targets
intestinal obstructionOpen Targets
attention deficit hyperactivity disorderOpen Targets
attention deficit-hyperactivity disorder 8Open Targets
hereditary attention deficit-hyperactivity disorderOpen Targets
intellectual disability, autosomal recessive 59Open Targets
movement disorderOpen Targets
schizophrenia 15Open Targets
Phelan-McDermid syndromeOpen Targets
Tourette syndromeOpen Targets
corneal dystrophyOpen Targets
X-linked non-syndromic intellectual disabilityOpen Targets
intellectual disability, autosomal dominant 50Open Targets
Potocki-Lupski syndromeOpen Targets
FRAXE intellectual disabilityOpen Targets
X-linked dominant intellectual disability - epilepsy syndromeOpen Targets
intellectual developmental disorder, X-linked, syndromic, Pilorge typeOpen Targets
Smith-Magenis syndromeOpen Targets
No pathogenic variants reported on ClinVar for this gene.