MAP10

gene
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Also known as MTR120

Summary

MAP10 (microtubule associated protein 10, HGNC:29265) is a protein-coding gene on chromosome 1q42.2, encoding Microtubule-associated protein 10 (Q9P2G4). Microtubule-associated protein (MAP) that plays a role in the regulation of cell division; promotes microtubule stability and participates in the organization of the spindle midzone and normal progress of cytokinesis.

Enables microtubule binding activity. Involved in microtubule cytoskeleton organization; positive regulation of cytokinesis; and regulation of microtubule-based process. Located in microtubule cytoskeleton and midbody.

Source: NCBI Gene 54627 — RefSeq curated summary.

At a glance

  • GWAS associations: 4
  • Clinical variants (ClinVar): 179 total
  • MANE Select transcript: NM_019090

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:29265
Approved symbolMAP10
Namemicrotubule associated protein 10
Location1q42.2
Locus typegene with protein product
StatusApproved
AliasesMTR120
Ensembl geneENSG00000212916
Ensembl biotypeprotein_coding
OMIM618551
Entrez54627

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000418460

RefSeq mRNA: 1 — MANE Select: NM_019090 NM_019090

CCDS: CCDS44334

Canonical transcript exons

ENST00000418460 — 1 exons

ExonStartEnd
ENSE00001623286232805416232809929

Expression profiles

Bgee: expression breadth ubiquitous, 130 present calls, max score 80.74.

FANTOM5 (CAGE): breadth broad, TPM avg 1.6708 / max 59.4992, expressed in 871 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
90711.0778623
90700.5930335

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047380.74gold quality
islet of LangerhansUBERON:000000673.74gold quality
cortical plateUBERON:000534373.33gold quality
calcaneal tendonUBERON:000370170.39gold quality
skeletal muscle tissueUBERON:000113469.71gold quality
leukocyteCL:000073869.57gold quality
monocyteCL:000057669.56gold quality
hindlimb stylopod muscleUBERON:000425268.69gold quality
muscle tissueUBERON:000238568.34gold quality
ganglionic eminenceUBERON:000402367.91gold quality
endometriumUBERON:000129567.88gold quality
pancreasUBERON:000126467.17gold quality
muscle of legUBERON:000138366.92gold quality
prefrontal cortexUBERON:000045166.83gold quality
smooth muscle tissueUBERON:000113566.79gold quality
superior frontal gyrusUBERON:000266166.56gold quality
ventricular zoneUBERON:000305366.54gold quality
lymph nodeUBERON:000002966.43gold quality
gastrocnemiusUBERON:000138866.14gold quality
heart left ventricleUBERON:000208465.47gold quality
apex of heartUBERON:000209864.80gold quality
duodenumUBERON:000211464.63gold quality
primary visual cortexUBERON:000243664.51gold quality
granulocyteCL:000009464.24gold quality
body of pancreasUBERON:000115064.19gold quality
right lobe of liverUBERON:000111463.86gold quality
gall bladderUBERON:000211063.75gold quality
frontal cortexUBERON:000187063.68gold quality
heartUBERON:000094863.56gold quality
liverUBERON:000210763.10gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-MTAB-6386no142.15
E-ANND-3no2.19

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

116 targeting MAP10, 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-4476100.0068.182030
HSA-MIR-6876-5P100.0067.682126
HSA-MIR-5692A100.0074.406850
HSA-MIR-518D-5P100.0067.51979
HSA-MIR-518E-5P100.0067.66954
HSA-MIR-518F-5P100.0067.51979
HSA-MIR-519A-5P100.0067.66954
HSA-MIR-519B-5P100.0067.66954
HSA-MIR-519C-5P100.0067.66954
HSA-MIR-520C-5P100.0067.51979
HSA-MIR-522-5P100.0067.66954
HSA-MIR-523-5P100.0067.66954
HSA-MIR-526A-5P100.0067.51979
HSA-MIR-4262100.0073.263931
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-656-3P100.0072.152788
HSA-MIR-428299.9975.366408
HSA-MIR-181A-5P99.9972.962995
HSA-MIR-181B-5P99.9972.972996
HSA-MIR-181C-5P99.9972.952996
HSA-MIR-181D-5P99.9973.042997
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-1213699.9872.815713
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-548AA99.9670.643753
HSA-MIR-548AP-3P99.9670.643753
HSA-MIR-548T-3P99.9670.643753
HSA-MIR-590-3P99.9674.346478
HSA-MIR-1236-3P99.9468.041695

Literature-anchored findings (GeneRIF, showing 1)

  • these data suggest that MTR120 is a novel microtubule (MT)-associated protein that directly stabilizes MTs and hence ensures the fidelity of cell division. (PMID:23264731)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriomap10ENSDARG00000100261
mus_musculusMap10ENSMUSG00000050930
rattus_norvegicusMap10ENSRNOG00000028652

Protein

Protein identifiers

Microtubule-associated protein 10Q9P2G4 (reviewed: Q9P2G4)

Alternative names: Microtubule regulator of 120 KDa

All UniProt accessions (1): Q9P2G4

UniProt curated annotations — full annotation on UniProt →

Function. Microtubule-associated protein (MAP) that plays a role in the regulation of cell division; promotes microtubule stability and participates in the organization of the spindle midzone and normal progress of cytokinesis.

Subunit / interactions. Interacts (via middle region) with microtubules.

Subcellular location. Cytoplasm. Cytoskeleton. Spindle pole. Microtubule organizing center. Centrosome. Midbody.

Tissue specificity. Expressed in different cell lines (at protein level).

RefSeq proteins (1): NP_061963* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR026679MAP10_C-termDomain
IPR039302MAP10Family

Pfam: PF14924, PF14925

UniProt features (16 total): compositionally biased region 8, region of interest 7, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9P2G4-F150.700.10

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 103 (showing top): GOBP_CHROMOSOME_ORGANIZATION, GOBP_CYTOPLASMIC_MICROTUBULE_ORGANIZATION, GOBP_REGULATION_OF_MICROTUBULE_BASED_PROCESS, BOYLAN_MULTIPLE_MYELOMA_D_DN, GOCC_MICROTUBULE_ORGANIZING_CENTER, GOBP_MITOTIC_SPINDLE_ASSEMBLY, MODULE_205, GOBP_ORGANELLE_FISSION, GOBP_CYTOKINESIS, GOBP_POSITIVE_REGULATION_OF_CELL_DIVISION, GOBP_REGULATION_OF_CELL_CYCLE, GOCC_CENTROSOME, GOBP_MITOTIC_NUCLEAR_DIVISION, GOBP_POSITIVE_REGULATION_OF_CELL_CYCLE_PROCESS, GOBP_REGULATION_OF_CYTOKINESIS

GO Biological Process (6): cytoplasmic microtubule organization (GO:0031122), positive regulation of cytokinesis (GO:0032467), regulation of microtubule-based process (GO:0032886), mitotic spindle midzone assembly (GO:0051256), cell division (GO:0051301), microtubule cytoskeleton organization (GO:0000226)

GO Molecular Function (1): microtubule binding (GO:0008017)

GO Cellular Component (8): centrosome (GO:0005813), cytoplasmic microtubule (GO:0005881), midbody (GO:0030496), mitotic spindle pole (GO:0097431), mitotic spindle midzone (GO:1990023), spindle pole (GO:0000922), cytoplasm (GO:0005737), cytoskeleton (GO:0005856)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure3
microtubule-based process2
mitotic spindle2
microtubule cytoskeleton organization1
supramolecular fiber organization1
cytokinesis1
regulation of cytokinesis1
positive regulation of cell division1
positive regulation of cell cycle process1
regulation of cellular process1
mitotic spindle elongation1
spindle midzone assembly1
mitotic spindle assembly1
mitotic nuclear division1
mitotic cell cycle process1
cellular process1
cytoskeleton organization1
tubulin binding1
centriole1
microtubule organizing center1
cytoplasm1
microtubule1
spindle pole1
spindle midzone1
spindle1
intracellular anatomical structure1
intracellular membraneless organelle1

Protein interactions and networks

STRING

272 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MAP10TRAPPC14Q8WVR3618
MAP10ZNF133P52736532
MAP10RASGEF1CQ8N431491
MAP10ZNF584Q8IVC4479
MAP10MAP9Q49MG5479
MAP10ZSCAN2Q7Z7L9437
MAP10C3orf38Q5JPI3433
MAP10FOXD4L3Q6VB84419
MAP10FOXD4L4Q8WXT5417
MAP10KIAA0408Q6ZU52395
MAP10TEDC1Q86SX3392
MAP10LRRC61Q9BV99391
MAP10A6NDT3A6NDT3380
MAP10MTCL3Q5TF21374
MAP10BRINP1O60477351

IntAct

3 interactions, top by confidence:

ABTypeScore
MAP10HNRNPUpsi-mi:“MI:0915”(physical association)0.400
MAP10WDR62psi-mi:“MI:0914”(association)0.350

BioGRID (31): LOC100158003 (Reconstituted Complex), TUBB2A (Reconstituted Complex), MAP10 (Proximity Label-MS), AMER1 (Affinity Capture-MS), PRKACB (Affinity Capture-MS), WDR62 (Affinity Capture-MS), VPRBP (Affinity Capture-MS), MIB1 (Affinity Capture-MS), PRKAR1B (Affinity Capture-MS), CEP76 (Affinity Capture-MS), PPP1R15B (Affinity Capture-MS), CENPB (Affinity Capture-MS), CAMK2D (Affinity Capture-MS), KIAA0232 (Affinity Capture-MS), CWC22 (Affinity Capture-MS)

ESM2 similar proteins: A0A1L8EYB2, A0JMF7, A2AHC3, A3KMW7, A5D8S0, A5WUN7, B0S6S9, D3Z8E6, D3Z987, F1M5M3, F1MJR8, F1QB81, P70347, P97412, Q0P5X5, Q0VET5, Q15468, Q2M2Z5, Q2T9I9, Q3UEN2, Q3V0M2, Q49A88, Q49AJ0, Q5CZC0, Q5RA75, Q5RHB5, Q5SW75, Q5T5Y3, Q60664, Q6JPI3, Q6NRK3, Q6PUR7, Q71F56, Q76I76, Q7M6U3, Q7TSH4, Q8C753, Q8CCC3, Q8IWB6, Q8K2J4

Diamond homologs: A3KMW7, D3ZAP3, Q8BJS7, Q9P2G4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance155
Likely benign22
Benign2

Top pathogenic / likely-pathogenic (0)

SpliceAI

9 predictions. Top by Δscore:

VariantEffectΔscore
1:232806137:GCTGA:Gdonor_gain0.3900
1:232806368:A:AGacceptor_gain0.3900
1:232806198:TTAA:Tdonor_gain0.3300
1:232806266:TG:Tacceptor_gain0.3200
1:232805561:G:GTdonor_gain0.3000
1:232806267:G:GTacceptor_gain0.2400
1:232806268:T:TTacceptor_gain0.2400
1:232806269:T:TTacceptor_gain0.2400
1:232806070:C:Adonor_gain0.2000

AlphaMissense

6847 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000027515 (1:232803635 C>T), RS1001961203 (1:232809834 G>A), RS1002863802 (1:232805391 C>A,G,T), RS1003084684 (1:232808796 G>C), RS1003378542 (1:232808364 T>C), RS1003893187 (1:232810182 T>C), RS1004003932 (1:232810405 G>A), RS1004906704 (1:232808830 A>C), RS1004929316 (1:232809078 T>C), RS1007314972 (1:232806942 G>A,T), RS1008827128 (1:232809465 A>G,T), RS1009113810 (1:232803568 G>A), RS1009400552 (1:232808680 G>A), RS1009417011 (1:232803676 T>C), RS1009975622 (1:232805335 G>A,T)

Disease associations

OMIM: gene MIM:618551 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

4 associations (top):

StudyTraitp-value
GCST003472_12Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder5.000000e-07
GCST003472_13Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder4.000000e-07
GCST003472_14Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder3.000000e-07
GCST009391_1351Metabolite levels5.000000e-06

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0007679oppositional defiant disorder measurement
EFO:0010365lysophosphatidylcholine 22:6 measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

11 total (human), top 11 by PubMed support.

ChemicalActions (top 5)PubMed papers
3-((6-(2-methoxyphenyl)pyrimidin-4-yl)amino)phenyl)methane sulfonamidedecreases expression1
GSK-J4decreases expression1
triphenyl phosphateaffects expression1
bisphenol Adecreases expression1
cypermethrinincreases expression1
abrineincreases expression1
Benzo(a)pyreneaffects methylation, decreases methylation1
Tobacco Smoke Pollutiondecreases expression1
Valproic Aciddecreases methylation1
Aflatoxin B1increases methylation1
Okadaic Aciddecreases 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.