STMN4

gene
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Also known as RB3

Summary

STMN4 (stathmin 4, HGNC:16078) is a protein-coding gene on chromosome 8p21.2, encoding Stathmin-4 (Q9H169). Exhibits microtubule-destabilizing activity.

Predicted to enable tubulin binding activity. Predicted to be involved in microtubule depolymerization; neuron projection development; and regulation of microtubule polymerization or depolymerization. Predicted to be located in Golgi apparatus and growth cone. Predicted to be active in cytoplasm and neuron projection.

Source: NCBI Gene 81551 — RefSeq curated summary.

At a glance

  • GWAS associations: 3
  • Clinical variants (ClinVar): 24 total
  • MANE Select transcript: NM_030795

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:16078
Approved symbolSTMN4
Namestathmin 4
Location8p21.2
Locus typegene with protein product
StatusApproved
AliasesRB3
Ensembl geneENSG00000015592
Ensembl biotypeprotein_coding
OMIM620740
Entrez81551

Gene structure

Transcript identifiers

Ensembl transcripts: 11 — 10 protein_coding, 1 retained_intron

ENST00000265770, ENST00000350889, ENST00000519614, ENST00000519997, ENST00000522750, ENST00000522908, ENST00000523048, ENST00000908225, ENST00000908226, ENST00000955363, ENST00000955364

RefSeq mRNA: 10 — MANE Select: NM_030795 NM_001283053, NM_001283054, NM_001283055, NM_001394383, NM_001394384, NM_001394385, NM_001394386, NM_001394387, NM_001394388, NM_030795

CCDS: CCDS6055, CCDS64851, CCDS64852, CCDS64854

Canonical transcript exons

ENST00000350889 — 7 exons

ExonStartEnd
ENSE000010415412723997127240162
ENSE000010415462724105427241262
ENSE000018990752723530827236905
ENSE000021292972725835127258404
ENSE000035125032724167727241757
ENSE000036039372724239727242492
ENSE000036664982724371127243801

Expression profiles

Bgee: expression breadth ubiquitous, 177 present calls, max score 99.31.

FANTOM5 (CAGE): breadth broad, TPM avg 8.2625 / max 803.8024, expressed in 250 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
924387.5861240
924390.6763129

Top tissues by expression

274 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
cortical plateUBERON:000534399.31gold quality
C1 segment of cervical spinal cordUBERON:000646999.20gold quality
spinal cordUBERON:000224098.89gold quality
ganglionic eminenceUBERON:000402398.69gold quality
prefrontal cortexUBERON:000045198.60gold quality
middle temporal gyrusUBERON:000277198.45gold quality
right frontal lobeUBERON:000281098.31gold quality
Brodmann (1909) area 9UBERON:001354098.25gold quality
frontal cortexUBERON:000187098.11gold quality
frontal lobeUBERON:001652598.11gold quality
dorsolateral prefrontal cortexUBERON:000983498.08gold quality
hypothalamusUBERON:000189898.05gold quality
neocortexUBERON:000195098.04gold quality
ventricular zoneUBERON:000305398.00gold quality
amygdalaUBERON:000187697.92gold quality
cerebral cortexUBERON:000095697.86gold quality
primary visual cortexUBERON:000243697.84gold quality
Ammon’s hornUBERON:000195497.75gold quality
cingulate cortexUBERON:000302797.73gold quality
anterior cingulate cortexUBERON:000983597.73gold quality
medial globus pallidusUBERON:000247797.69gold quality
globus pallidusUBERON:000187597.58gold quality
lateral nuclear group of thalamusUBERON:000273697.50gold quality
Brodmann (1909) area 46UBERON:000648397.50gold quality
occipital lobeUBERON:000202197.45gold quality
inferior vagus X ganglionUBERON:000536397.42gold quality
telencephalonUBERON:000189397.41gold quality
right hemisphere of cerebellumUBERON:001489097.35gold quality
cerebellar cortexUBERON:000212997.30gold quality
cerebellar hemisphereUBERON:000224597.29gold quality

Single-cell (SCXA)

Detected in 10 experiment(s), a significant marker in 6.

ExperimentMarker?Max mean expression
E-MTAB-11121yes2539.51
E-MTAB-6911yes451.51
E-HCAD-5yes54.08
E-MTAB-7316yes13.60
E-GEOD-93593yes10.69
E-HCAD-10yes5.18
E-MTAB-8894no1623.43
E-MTAB-9154no1392.59
E-MTAB-7303no367.34
E-ANND-3no2.28

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

64 targeting STMN4, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-450A-1-3P100.0069.331837
HSA-MIR-4481100.0066.421669
HSA-MIR-3613-3P100.0076.367965
HSA-MIR-8485100.0077.574731
HSA-MIR-223-3P99.9970.141140
HSA-MIR-450B-5P99.9271.483175
HSA-MIR-4731-5P99.8967.232537
HSA-MIR-4671-3P99.8872.461045
HSA-MIR-518A-5P99.7069.012209
HSA-MIR-52799.7069.012209
HSA-MIR-119799.7067.751027
HSA-MIR-7154-5P99.6970.521900
HSA-MIR-6512-3P99.6566.071468
HSA-MIR-6720-5P99.6566.221459
HSA-MIR-488-3P99.6168.791731
HSA-MIR-3682-3P99.5867.63865
HSA-MIR-6722-3P99.4567.621919
HSA-MIR-239299.4367.50708
HSA-MIR-532-3P99.3465.761195
HSA-MIR-4652-3P99.3370.022742
HSA-MIR-6828-5P99.3169.211433
HSA-MIR-3692-5P99.2967.041421
HSA-MIR-4727-5P99.2367.551154
HSA-MIR-122B-3P99.2168.901333
HSA-MIR-21-3P99.2168.951312
HSA-MIR-427999.1966.702437
HSA-MIR-6815-3P99.1368.981530
HSA-MIR-4758-3P99.1263.96869
HSA-MIR-10524-5P99.0566.08963
HSA-MIR-1909-3P99.0366.561662

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriostmn4lENSDARG00000043932
mus_musculusStmn4ENSMUSG00000022044
rattus_norvegicusStmn4ENSRNOG00000053334
drosophila_melanogasterstaiFBGN0266521

Paralogs (4): STMN2 (ENSG00000104435), STMN1 (ENSG00000117632), STMN3 (ENSG00000197457), STMND1 (ENSG00000230873)

Protein

Protein identifiers

Stathmin-4Q9H169 (reviewed: Q9H169)

Alternative names: Stathmin-like protein B3

All UniProt accessions (3): Q9H169, E5RIR6, E7EVN3

UniProt curated annotations — full annotation on UniProt →

Function. Exhibits microtubule-destabilizing activity.

Subcellular location. Golgi apparatus. Cell projection. Growth cone. Axon.

Similarity. Belongs to the stathmin family.

Isoforms (4)

UniProt IDNamesCanonical?
Q9H169-11yes
Q9H169-22
Q9H169-33
Q9H169-44

RefSeq proteins (10): NP_001269982, NP_001269983, NP_001269984, NP_001381312, NP_001381313, NP_001381314, NP_001381315, NP_001381316, NP_001381317, NP_110422* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000956Stathmin_famFamily
IPR030514Stathmin_CSConserved_site
IPR036002Stathmin_sfHomologous_superfamily

Pfam: PF00836

UniProt features (15 total): splice variant 3, strand 2, helix 2, lipid moiety-binding region 2, chain 1, domain 1, sequence conflict 1, region of interest 1, coiled-coil region 1, modified residue 1

Structure

Experimental structures (PDB)

10 structures.

PDBMethodResolution (Å)
9F07X-RAY DIFFRACTION2.21
6O5MX-RAY DIFFRACTION2.3
6BR1X-RAY DIFFRACTION2.3
6NNGX-RAY DIFFRACTION2.4
6BRFX-RAY DIFFRACTION2.5
7CPDX-RAY DIFFRACTION2.51
6O61X-RAY DIFFRACTION2.6
6PC4X-RAY DIFFRACTION2.6
6BRYX-RAY DIFFRACTION2.7
6O5NX-RAY DIFFRACTION3

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9H169-F184.520.58

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (3): 90, 20, 22

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 130 (showing top): GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_DN, GNF2_RTN1, GOBP_REGULATION_OF_MICROTUBULE_BASED_PROCESS, AAGCCAT_MIR135A_MIR135B, GOBP_NEUROGENESIS, GGGTGGRR_PAX4_03, EFC_Q6, CDP_01, chr8p21, GOBP_MICROTUBULE_DEPOLYMERIZATION, NF1_Q6_01, TGCTGAY_UNKNOWN, TGACATY_UNKNOWN, AACTTT_UNKNOWN, GOBP_PROTEIN_DEPOLYMERIZATION

GO Biological Process (3): microtubule depolymerization (GO:0007019), regulation of microtubule polymerization or depolymerization (GO:0031110), neuron projection development (GO:0031175)

GO Molecular Function (2): tubulin binding (GO:0015631), protein binding (GO:0005515)

GO Cellular Component (6): cytoplasm (GO:0005737), Golgi apparatus (GO:0005794), growth cone (GO:0030426), neuron projection (GO:0043005), axon (GO:0030424), cell projection (GO:0042995)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
microtubule polymerization or depolymerization2
cellular anatomical structure2
protein depolymerization1
supramolecular fiber organization1
regulation of microtubule cytoskeleton organization1
neuron development1
plasma membrane bounded cell projection organization1
cytoskeletal protein binding1
binding1
intracellular anatomical structure1
cytoplasm1
endomembrane system1
intracellular membrane-bounded organelle1
site of polarized growth1
distal axon1
plasma membrane bounded cell projection1
neuron projection1

Protein interactions and networks

STRING

1860 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
STMN4TTLQ8NG68577
STMN4TUBA1BP04687541
STMN4GNG3P29798490
STMN4FHIP2BQ86V87459
STMN4ACSBG1Q96GR2436
STMN4SLC32A1Q9H598395
STMN4SNRPNP14648369
STMN4SLC1A2P43004363
STMN4ABLIM2Q6H8Q1348
STMN4RGSL1A5PLK6340
STMN4TBCAO75347327
STMN4SAXO1Q8IYX7302
STMN4TUBD1Q9UJT1289
STMN4KIF9Q9HAQ2288
STMN4UBE3AP78355285
STMN4CDK5RAP3Q96JB5285

IntAct

8 interactions, top by confidence:

ABTypeScore
STMN4ANKRD13Apsi-mi:“MI:0915”(physical association)0.400
STMN4MTNR1Bpsi-mi:“MI:0915”(physical association)0.370
STMN4NUFIP2psi-mi:“MI:0915”(physical association)0.370
MAPTSHTN1psi-mi:“MI:0914”(association)0.350
STMN4TRAPPC3psi-mi:“MI:0914”(association)0.350
STMN4IMMTpsi-mi:“MI:0915”(physical association)0.000
STMN4PHIPpsi-mi:“MI:0915”(physical association)0.000

BioGRID (51): C7orf43 (Affinity Capture-MS), TRAPPC9 (Affinity Capture-MS), TRAPPC6B (Affinity Capture-MS), TRAPPC10 (Affinity Capture-MS), STMN4 (Affinity Capture-MS), TRAPPC4 (Affinity Capture-MS), VTA1 (Affinity Capture-MS), TRAPPC1 (Affinity Capture-MS), TRAPPC3 (Affinity Capture-MS), TRAPPC2 (Affinity Capture-MS), TRAPPC5 (Affinity Capture-MS), PTPRD (Affinity Capture-MS), GCA (Affinity Capture-MS), STMN4 (Two-hybrid), STMN4 (Affinity Capture-Western)

ESM2 similar proteins: A0A088MLT8, A2AQ19, A4FV29, A4IFK9, B3KU38, O14795, O70166, O93388, O95983, P21818, P31395, P50751, P54227, P55821, P63042, P63043, Q09001, Q09002, Q09004, Q09006, Q2KJ58, Q32L68, Q4KUS2, Q4R4N5, Q5F3L9, Q5FVJ5, Q5PSV4, Q5R4C5, Q5R562, Q5R8C6, Q5RAD5, Q62768, Q6GQB5, Q8IVM0, Q8IW50, Q8TBN0, Q8VDV3, Q90987, Q92541, Q93045

Diamond homologs: A4IFK9, A9YWH3, O70166, O93388, P13668, P16949, P21818, P31395, P54227, P55821, P63042, P63043, Q09001, Q09002, Q09004, Q09005, Q09006, Q3T0C7, Q4R4N5, Q4R712, Q5R4C5, Q5R8C6, Q6DUB7, Q90987, Q93045, Q9H169, Q9JHU6, Q9NZ72

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

24 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance19
Likely benign1
Benign2

Top pathogenic / likely-pathogenic (0)

SpliceAI

852 predictions. Top by Δscore:

VariantEffectΔscore
8:27236901:TTGTC:Tacceptor_gain1.0000
8:27236902:TGTC:Tacceptor_gain1.0000
8:27236903:GTC:Gacceptor_gain1.0000
8:27236904:TC:Tacceptor_gain1.0000
8:27236905:CC:Cacceptor_gain1.0000
8:27236906:C:CCacceptor_gain1.0000
8:27236906:CT:Cacceptor_loss1.0000
8:27239965:CCTCA:Cdonor_loss1.0000
8:27239966:CTCA:Cdonor_loss1.0000
8:27239967:TCA:Tdonor_loss1.0000
8:27239968:CA:Cdonor_loss1.0000
8:27239969:ACCT:Adonor_loss1.0000
8:27239970:CCTT:Cdonor_gain1.0000
8:27240012:C:Adonor_gain1.0000
8:27240161:TA:Tacceptor_gain1.0000
8:27240163:C:CCacceptor_gain1.0000
8:27240163:C:CGacceptor_loss1.0000
8:27240164:T:Cacceptor_loss1.0000
8:27240172:C:CTacceptor_gain1.0000
8:27240173:A:ACacceptor_gain1.0000
8:27240173:A:Cacceptor_gain1.0000
8:27241049:TTTAC:Tdonor_loss1.0000
8:27241050:TTAC:Tdonor_loss1.0000
8:27241051:TACCT:Tdonor_loss1.0000
8:27241052:A:ACdonor_gain1.0000
8:27241052:ACC:Adonor_loss1.0000
8:27241052:ACCTT:Adonor_gain1.0000
8:27241053:C:CCdonor_gain1.0000
8:27241053:CCTT:Cdonor_gain1.0000
8:27241053:CCTTC:Cdonor_gain1.0000

AlphaMissense

1433 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
8:27241180:A:CF64L0.999
8:27241180:A:TF64L0.999
8:27241182:A:GF64L0.999
8:27239981:A:GL167P0.998
8:27239997:C:GA162P0.998
8:27240009:C:GA158P0.998
8:27240060:C:GA141P0.998
8:27240122:C:GR120P0.998
8:27241057:C:AR105S0.998
8:27241057:C:GR105S0.998
8:27241061:C:GR104P0.998
8:27241071:C:GA101P0.998
8:27236883:C:GR178P0.997
8:27236896:C:GA174P0.997
8:27239984:C:GR166P0.997
8:27240000:C:GA161P0.997
8:27240002:A:GL160P0.997
8:27240013:C:AR156S0.997
8:27240013:C:GR156S0.997
8:27240047:A:GL145P0.997
8:27240093:C:GA130P0.997
8:27240143:A:GL113P0.997
8:27240153:C:GA110P0.997
8:27241070:G:TA101D0.997
8:27241074:C:GA100P0.997
8:27241079:A:GL98P0.997
8:27241169:A:GL68P0.997
8:27240134:A:GL116P0.996
8:27241058:C:GR105T0.996
8:27241175:A:TV66D0.996

dbSNP variants (sampled 300 via entrez): RS1000107120 (8:27252363 A>C,G), RS1000145256 (8:27238044 C>T), RS1000145487 (8:27259070 C>G), RS1000160648 (8:27245932 A>G), RS1000382245 (8:27240274 G>A), RS1000409934 (8:27250565 G>A), RS1000452933 (8:27239501 C>T), RS1000477859 (8:27251569 T>C), RS1000505085 (8:27235690 C>A,T), RS1000599610 (8:27235436 T>G), RS1000816636 (8:27240612 T>C), RS1000892163 (8:27246272 G>A), RS1000958623 (8:27251955 C>A), RS1000999853 (8:27256788 T>C), RS1001055044 (8:27241212 C>G,T)

Disease associations

OMIM: gene MIM:620740 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

3 associations (top):

StudyTraitp-value
GCST009377_2Bone mineral density2.000000e-07
GCST009378_11Bone mineral content7.000000e-07
GCST009378_7Bone mineral content6.000000e-06

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0007620volumetric bone mineral density
EFO:0007621bone mineral content measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

20 total (human), top 20 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, decreases expression, increases expression4
Cadmium Chloridedecreases expression, increases expression3
Benzo(a)pyreneincreases expression, increases methylation, affects methylation2
methylmercuric chloridedecreases expression1
arsenitedecreases methylation1
mono-(2-ethylhexyl)phthalatedecreases expression1
butyraldehydeincreases expression1
15-acetyldeoxynivalenolincreases expression1
entinostatdecreases expression1
abrineincreases expression1
Decitabineaffects expression1
Amphotericin Bincreases expression1
Cisplatinaffects expression1
Cytarabineincreases response to substance1
Diethylhexyl Phthalatedecreases expression1
N-Nitrosopyrrolidineincreases expression1
Niclosamideincreases expression1
Aflatoxin B1increases expression1
Okadaic Acidincreases expression1
Acrylamidedecreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.