1 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.
8PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITYβ Experimental GO Evidenceβ Swiss-Prot Reviewed
neuromuscular synaptic transmissionmanchettebenzodiazepine receptor bindingspermatid developmentneurodegenerative diseaseazoospermiapartial chromosome Y deletionspermatogenic failure 78
Based on limited published evidence, RIMBP3C is a probable component of the manchette, a microtubule-based structure essential for sperm head morphogenesis during late spermatid development. GO annotations indicate roles in spermatid development, fertilization, and benzodiazepine receptor binding. A single study identified RIMBP3C as a hub gene associated with sunitinib response and immune infiltration in clear cell renal cell carcinoma 1, though this appears to be a bioinformatic finding rather than direct functional characterization.
1
RIMBP3C identified as a hub gene related to sunitinib resistance and immune infiltration in clear cell renal cell carcinoma through co-expression network analysis
PMID: 34402193β Limited data available β This gene has 1 indexed publication. Summary and analysis may be incomplete.
neurodegenerative diseaseOpen Targets
partial chromosome Y deletionOpen Targets
spermatogenic failure 78Open Targets
spermatogenic failure 20Open Targets
spermatogenic failure, X-linked, 3Open Targets
spermatogenic failure 54Open Targets
spermatogenic failure 40Open Targets
spermatogenic failure 10Open Targets
spermatogenic failure 11Open Targets
spermatogenic failure 76Open Targets
spermatogenic failure 80Open Targets
spermatogenic failure 47Open Targets
spermatogenic failure 65Open Targets
spermatogenic failure 72Open Targets
spermatogenic failure 39Open Targets
spermatogenic failure 84Open Targets
spermatogenic failure 93Open Targets
spermatogenic failure 18Open Targets
spermatogenic failure 27Open Targets
No pathogenic variants reported on ClinVar for this gene.