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GeneE
2 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
β“˜GeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
STMND1
stathmin domain containing 1
Chromosome 6 Β· 6p22.3
NCBI Gene: 401236Ensembl: ENSG00000230873.10HGNC: HGNC:44668UniProt: H3BQB6
3PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
tubulin bindingmicrotubule depolymerizationregulation of microtubule polymerization or depolymerizationneuron projection developmentneurodegenerative diseasemathematical abilitysmoking initiationmajor depressive disorder
✦AI Summary

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.

Sources cited
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: 38630521
⚠Limited data available β€” This gene has 1 indexed publication. Summary and analysis may be incomplete.
Disease Associationsβ“˜20
neurodegenerative diseaseOpen Targets
0.40Moderate
mathematical abilityOpen Targets
0.39Weak
smoking initiationOpen Targets
0.34Weak
major depressive disorderOpen Targets
0.33Weak
anxiety disorderOpen Targets
0.28Weak
alcohol drinkingOpen Targets
0.28Weak
intelligenceOpen Targets
0.28Weak
gastroesophageal reflux diseaseOpen Targets
0.27Weak
generalised epilepsyOpen Targets
0.27Weak
Chest painOpen Targets
0.27Weak
preeclampsiaOpen Targets
0.26Weak
poisoningOpen Targets
0.21Weak
systemic lupus erythematosusOpen Targets
0.20Weak
tongue cancerOpen Targets
0.19Weak
Atypical behaviorOpen Targets
0.19Weak
neuroendocrine neoplasmOpen Targets
0.17Weak
ovarian dysfunctionOpen Targets
0.15Weak
response to xenobiotic stimulusOpen Targets
0.13Weak
ProptosisOpen Targets
0.11Weak
metabolic syndromeOpen Targets
0.07Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar β†—
Related Genes
STMN4Shared pathway100%STMN3Shared pathway43%STMN1Shared pathway38%STMN2Shared pathway33%GPRIN2Shared pathway33%GPRIN1Shared pathway33%
Tissue Expression6 tissues
Brain
100%
Lung
19%
Liver
6%
Ovary
4%
Bone Marrow
1%
Heart
0%
Gene Interaction Network
Click a node to explore
STMND1STMN4STMN3STMN1STMN2GPRIN2GPRIN1
PROTEIN STRUCTURE
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AlphaFoldAI-predicted Β· UniProt H3BQB6
View on AlphaFold β†—
Constraintβ“˜
LOEUFβ“˜
1.15LoF Tolerant
pLIβ“˜
0.00Tolerant
Observed/Expected LoF0.77 [0.53–1.15]
RankingsWhere STMND1 stands among ~20K protein-coding genes
  • #19,036of 20,598
    Most Researched3
  • #11,923of 17,882
    Most Constrained (LOEUF)1.15
Genes detectedSTMND1
Sources retrieved2 papers
Response timeβ€”
πŸ“„ Sources
2
1
Nuclear spheres modulate the expression of BEST1 and GADD45G.
PMID: 26521045
Cell Signal Β· 2016
1.00
2
STMND1 is a phylogenetically ancient stathmin which localizes to motile cilia and exhibits nuclear translocation that is inhibited when soluble tubulin concentration increases.
PMID: 38630521
Mol Biol Cell Β· 2024
0.50