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.
3PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITYβ Experimental GO Evidenceβ Swiss-Prot Reviewed
tubulin bindingmicrotubule depolymerizationregulation of microtubule polymerization or depolymerizationneuron projection developmentneurodegenerative diseasemathematical abilitysmoking initiationmajor depressive disorder
Based on limited published evidence, STMND1 (stathmin domain containing 1) is a phylogenetically ancient stathmin protein that binds tubulin dimers and localizes to motile cilia 1. The protein features a N-terminal myristoylated and palmitoylated motif directing membrane localization and a tubulin-binding stathmin-like domain containing an internal nuclear localization signal 1. STMND1 exhibits tubulin-dependent nuclear translocation, with soluble tubulin concentration inhibiting this translocation 1. Highly expressed in multiciliated epithelial cells, STMND1 overexpression increases primary cilia length 1. GO annotations suggest involvement in microtubule depolymerization and regulation of microtubule polymerization, with roles in neuronal development.
1
Characterized STMND1 as ancient stathmin with tubulin-binding capability, membrane localization via lipid modifications, tubulin-inhibited nuclear translocation, ciliary localization, and cilia-lengthening function when overexpressed
PMID: 38630521β Limited data available β This gene has 1 indexed publication. Summary and analysis may be incomplete.
neurodegenerative diseaseOpen Targets
mathematical abilityOpen Targets
smoking initiationOpen Targets
major depressive disorderOpen Targets
anxiety disorderOpen Targets
alcohol drinkingOpen Targets
gastroesophageal reflux diseaseOpen Targets
generalised epilepsyOpen Targets
systemic lupus erythematosusOpen Targets
tongue cancerOpen Targets
Atypical behaviorOpen Targets
neuroendocrine neoplasmOpen Targets
ovarian dysfunctionOpen Targets
response to xenobiotic stimulusOpen Targets
metabolic syndromeOpen Targets
No pathogenic variants reported on ClinVar for this gene.