MOV10

gene
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Also known as gb110MGC2948fSAP113

Summary

MOV10 (Mov10 RNA helicase, HGNC:7200) is a protein-coding gene on chromosome 1p13.2, encoding Helicase MOV-10 (Q9HCE1). 5’ to 3’ RNA helicase that is involved in a number of cellular roles ranging from mRNA metabolism and translation, modulation of viral infectivity, inhibition of retrotransposition, or regulation of synaptic transmission.

Enables 5’-3’ RNA helicase activity and RNA binding activity. Involved in defense response to virus and mRNA destabilization. Located in P-body and cytosol. Implicated in hypertension.

Source: NCBI Gene 4343 — RefSeq curated summary.

At a glance

  • GWAS associations: 44
  • Clinical variants (ClinVar): 153 total
  • Dosage sensitivity (ClinGen): haploinsufficiency no evidence, triplosensitivity no evidence
  • MANE Select transcript: NM_001321324

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:7200
Approved symbolMOV10
NameMov10 RNA helicase
Location1p13.2
Locus typegene with protein product
StatusApproved
Aliasesgb110, MGC2948, fSAP113
Ensembl geneENSG00000155363
Ensembl biotypeprotein_coding
OMIM610742
Entrez4343

Gene structure

Transcript identifiers

Ensembl transcripts: 41 — 21 protein_coding, 12 retained_intron, 7 protein_coding_CDS_not_defined, 1 nonsense_mediated_decay

ENST00000357443, ENST00000369644, ENST00000369645, ENST00000413052, ENST00000465579, ENST00000468624, ENST00000471160, ENST00000475429, ENST00000481711, ENST00000482545, ENST00000486416, ENST00000488160, ENST00000490413, ENST00000494319, ENST00000495374, ENST00000496577, ENST00000685268, ENST00000686097, ENST00000686428, ENST00000686923, ENST00000687174, ENST00000687333, ENST00000687509, ENST00000688698, ENST00000689955, ENST00000690243, ENST00000885023, ENST00000885024, ENST00000885025, ENST00000885026, ENST00000885027, ENST00000885028, ENST00000923694, ENST00000923695, ENST00000923696, ENST00000923697, ENST00000923698, ENST00000923699, ENST00000923700, ENST00000948326, ENST00000948327

RefSeq mRNA: 7 — MANE Select: NM_001321324 NM_001130079, NM_001286072, NM_001321324, NM_001369507, NM_001389562, NM_001389563, NM_020963

CCDS: CCDS65615, CCDS853

Canonical transcript exons

ENST00000369645 — 21 exons

ExonStartEnd
ENSE00001450533112674659112674729
ENSE00003482274112689415112689650
ENSE00003498268112696630112696846
ENSE00003510951112698287112698478
ENSE00003524822112699894112699982
ENSE00003527691112694018112694172
ENSE00003544567112699685112699810
ENSE00003548185112691665112691799
ENSE00003553261112696437112696534
ENSE00003581241112700416112700739
ENSE00003593110112695416112695574
ENSE00003599353112697994112698111
ENSE00003600039112688935112689138
ENSE00003612006112694453112694629
ENSE00003619902112692761112692929
ENSE00003635003112689840112690098
ENSE00003649727112694749112694896
ENSE00003649924112700219112700340
ENSE00003671190112698715112698789
ENSE00003676444112674848112675049
ENSE00003688316112696148112696251

Expression profiles

Bgee: expression breadth ubiquitous, 232 present calls, max score 97.14.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 21.0284 / max 101.8844, expressed in 1815 samples.

FANTOM5 promoters (10 alternative TSS)

Promoter IDTPM avgSamples expressed
46934.25341530
46964.13131548
46983.00221352
46992.26861156
47001.94221180
46921.86541103
46951.4218893
46971.0645616
46940.7212436
47010.3576174

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right testisUBERON:000453497.14gold quality
left testisUBERON:000453396.84gold quality
right uterine tubeUBERON:000130296.48gold quality
adenohypophysisUBERON:000219696.39gold quality
right lobe of liverUBERON:000111496.21gold quality
granulocyteCL:000009495.76gold quality
lower esophagus mucosaUBERON:003583495.64gold quality
upper arm skinUBERON:000426395.61gold quality
skin of abdomenUBERON:000141695.56gold quality
mucosa of transverse colonUBERON:000499195.40gold quality
right adrenal gland cortexUBERON:003582795.27gold quality
right adrenal glandUBERON:000123395.14gold quality
metanephros cortexUBERON:001053395.11gold quality
pituitary glandUBERON:000000795.03gold quality
testisUBERON:000047394.87gold quality
right ovaryUBERON:000211894.80gold quality
skin of legUBERON:000151194.79gold quality
spleenUBERON:000210694.61gold quality
right lobe of thyroid glandUBERON:000111994.50gold quality
left adrenal gland cortexUBERON:003582594.39gold quality
endocervixUBERON:000045894.35gold quality
left adrenal glandUBERON:000123494.35gold quality
left ovaryUBERON:000211994.35gold quality
small intestine Peyer’s patchUBERON:000345494.34gold quality
left uterine tubeUBERON:000130394.31gold quality
ectocervixUBERON:001224994.11gold quality
olfactory segment of nasal mucosaUBERON:000538693.96gold quality
body of uterusUBERON:000985393.84gold quality
apex of heartUBERON:000209893.62gold quality
adrenal cortexUBERON:000123593.55gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes5.65

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

31 targeting MOV10, 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-4692100.0067.322066
HSA-MIR-451499.9967.101870
HSA-MIR-497-5P99.9271.832674
HSA-MIR-15A-5P99.9072.802787
HSA-MIR-15B-5P99.9072.782798
HSA-MIR-16-5P99.9072.802780
HSA-MIR-195-5P99.9072.812805
HSA-MIR-424-5P99.8971.902641
HSA-MIR-6838-5P99.8971.942690
HSA-MIR-6875-3P99.8270.262983
HSA-MIR-3680-3P99.7572.513095
HSA-MIR-1213099.7565.47452
HSA-MIR-548AU-3P99.7068.221373
HSA-MIR-64699.6867.841645
HSA-MIR-4524A-5P99.5771.731193
HSA-MIR-4524B-5P99.5771.681195
HSA-MIR-6722-3P99.4567.621919
HSA-MIR-450599.2767.812678
HSA-MIR-578799.2267.862628
HSA-MIR-361-3P99.1966.451381
HSA-MIR-3940-5P99.1465.26493
HSA-MIR-450799.1465.27515
HSA-MIR-1909-3P99.0366.561662
HSA-MIR-153-3P98.9672.511644
HSA-MIR-374B-3P98.6368.241360
HSA-MIR-138-5P98.4370.491292
HSA-MIR-6842-3P98.0766.331325
HSA-MIR-503-5P97.8766.83575
HSA-MIR-365297.7165.431890
HSA-MIR-443097.4765.611813

Functional genomics

ClinGen dosage: haploinsufficiency 0 (no evidence), triplosensitivity 0 (no evidence). ClinGen Gene Dosage Map

Literature-anchored findings (GeneRIF, showing 29)

  • Mov10 coimmunoprecipitates with human Ago1 and Ago2 and also colocalizes with them in cytoplasmic P-bodies. (PMID:16289642)
  • The identification of capped small RNAs and the involvement of MOV10 in hepatitis delta virus replication further suggest a conserved mechanism related to RNA-directed transcription in lower eukaryotes. (PMID:18552826)
  • These data suggest that MOV10 is involved in the progression of telomerase-catalyzing reaction via the interaction of telomerase protein and telomere DNA. (PMID:19665004)
  • Results suggest that Mov10 could be required during the lentiviral lifecycle and that its perturbation disrupts generation of infectious viral particles. (PMID:20140200)
  • MOV10, co-purifies and interacts with components of Polycomb-repressive complex 1 from human cells. Knockdown of MOV10 in human fibroblasts leads to the upregulation of the INK4a. (PMID:20543829)
  • identified two critical MOV10 packaging determinants and eight other critical residues for anti-HIV-1 activity (PMID:22105071)
  • Depletion of endogenous MOV10 significantly enhances the retrotransposition of endogenous retroelements. (PMID:22727223)
  • APOBEC3G inhibits microRNA-mediated repression of translation by interfering with the interaction between Argonaute-2 and MOV10 (PMID:22791714)
  • MOV10 contributes to the cellular control of long interspersed element 1 replication. (PMID:23754279)
  • Authors conclude that HIV-1 virion incorporation and the antiviral activities of Mov10 and APOBEC3G do not require their localization to P bodies. (PMID:23926332)
  • Association of the SNP rs2932538 in MOV10 and SNP rs4373814 in CACNB2 with an increased risk of hypertension in a Chinese Han population. (PMID:24338417)
  • Results show that MOV10 predominantly binds to 3’ UTRs upstream of regions predicted to form local secondary structures and provide evidence that MOV10 helicase mutants are impaired in their ability to translocate 5’ to 3’ on their mRNA targets. (PMID:24726324)
  • A dual function for MOV10 in regulating translation: it facilitates microRNA-mediated translation of some RNAs, but it also increases expression of other RNAs by preventing AGO2 function. (PMID:25464849)
  • The endogenous Mov10 could promote hepatitis B virus replication in vitro. (PMID:25533532)
  • The DEAG-box of huamn MOV10 was required for the enhancement of Rev/RRE-dependent nuclear export. (PMID:26379090)
  • MOV10 acts as an anti-influenza virus factor through specifically inhibiting the nuclear transportation of nucleoprotein and subsequently inhibiting the function of the viral ribonucleoprotein complex (PMID:26842467)
  • these results establish MOV10, an evolutionary conserved protein involved in RNA silencing, as an antiviral gene against RNA viruses that uses an retinoic acid-inducible gene I-like receptor-independent pathway to enhance IFN response (PMID:27016603)
  • MOV10 is a highly conserved cellular protein belonging to SF1 helicase family that plays critical roles in EV71 infection (PMID:27666477)
  • IRAV is an RNA binding protein and localizes to cytoplasmic processing bodies (P bodies) in uninfected cells, where it interacts with the MOV10 RISC complex RNA helicase, suggesting a role for IRAV in the processing of viral RNA. (PMID:27974568)
  • Through interference with the ubiquitin-proteasome system, MOV10 enhances the level of apolipoprotein-B-mRNA-editing enzyme catalytic polypeptide-like 3G in HIV-1-infected cells and virions, and synergistically inhibits the replication and infectivity of HIV-1. (PMID:29258557)
  • MOV10 interacts with RNASEH2, and their interplay is crucial for restricting L1 retrotransposition. (PMID:29315404)
  • the antiviral activity of MOV10 is partially countered by viral NS1 protein that interferes with the interaction of MOV10 with viral NP and causes MOV10 degradation through the lysosomal pathway. (PMID:30617221)
  • MOV10 / circ-DICER1 / miR-103a-3p (miR-382-5p) / ZIC4 pathway plays a vital role in regulating the angiogenesis of glioma. (PMID:30621721)
  • MOV10 restricts hepatitis B virus replication by inhibiting viral reverse transcription (PMID:31722967)
  • The association of MOV10 polymorphism and expression levels with preeclampsia in the Chinese Han population. (PMID:33269545)
  • Association study of hypertension susceptibility genes ITGA9, MOV10, and CACNB2 with preeclampsia in Chinese Han population. (PMID:33491517)
  • CRL4-DCAF12 Ubiquitin Ligase Controls MOV10 RNA Helicase during Spermatogenesis and T Cell Activation. (PMID:34065512)
  • MOV10 recruits DCP2 to decap human LINE-1 RNA by forming large cytoplasmic granules with phase separation properties. (PMID:37437058)
  • S100A16 stabilizes the ITGA3-mediated ECM-receptor interaction pathway to drive the malignant properties of lung adenocarcinoma cells via binding MOV10. (PMID:39450567)

Cross-species orthologs

8 orthologs

OrganismSymbolGene ID
danio_reriomov10aENSDARG00000015829
danio_reriomov10b.2ENSDARG00000056065
danio_reriomov10b.1ENSDARG00000061177
mus_musculusMov10ENSMUSG00000002227
rattus_norvegicusMov10ENSRNOG00000012946
caenorhabditis_elegansY106G6D.5WBGENE00014965
caenorhabditis_eleganssosi-1WBGENE00016565
caenorhabditis_eleganseri-7WBGENE00016566

Paralogs (10): UPF1 (ENSG00000005007), AQR (ENSG00000021776), MOV10L1 (ENSG00000073146), SETX (ENSG00000107290), ZNFX1 (ENSG00000124201), HELZ2 (ENSG00000130589), IGHMBP2 (ENSG00000132740), DNA2 (ENSG00000138346), CT55 (ENSG00000169551), HELZ (ENSG00000198265)

Protein

Protein identifiers

Helicase MOV-10Q9HCE1 (reviewed: Q9HCE1)

Alternative names: Armitage homolog, Moloney leukemia virus 10 protein

All UniProt accessions (5): Q9HCE1, A0A8I5KXC3, A0A8I5KZ07, A0A8I5QKW4, Q5JR04

UniProt curated annotations — full annotation on UniProt →

Function. 5’ to 3’ RNA helicase that is involved in a number of cellular roles ranging from mRNA metabolism and translation, modulation of viral infectivity, inhibition of retrotransposition, or regulation of synaptic transmission. Plays an important role in innate antiviral immunity by promoting type I interferon production. Mechanistically, specifically uses IKKepsilon/IKBKE as the mediator kinase for IRF3 activation. Blocks HIV-1 virus replication at a post-entry step. Counteracts HIV-1 Vif-mediated degradation of APOBEC3G through its helicase activity by interfering with the ubiquitin-proteasome pathway. Also inhibits hepatitis B virus/HBV replication by interacting with HBV RNA and thereby inhibiting the early step of viral reverse transcription. Contributes to UPF1 mRNA target degradation by translocation along 3’ UTRs. Required for microRNA (miRNA)-mediated gene silencing by the RNA-induced silencing complex (RISC). Required for both miRNA-mediated translational repression and miRNA-mediated cleavage of complementary mRNAs by RISC. In cooperation with FMR1, regulates miRNA-mediated translational repression by AGO2. Restricts retrotransposition of long interspersed element-1 (LINE-1) in cooperation with TUT4 and TUT7 counteracting the RNA chaperonne activity of L1RE1. Facilitates LINE-1 uridylation by TUT4 and TUT7. Required for embryonic viability and for normal central nervous system development and function. Plays two critical roles in early brain development: suppresses retroelements in the nucleus by directly inhibiting cDNA synthesis, while regulates cytoskeletal mRNAs to influence neurite outgrowth in the cytosol. May function as a messenger ribonucleoprotein (mRNP) clearance factor. (Microbial infection) Required for RNA-directed transcription and replication of the human hepatitis delta virus (HDV). Interacts with small capped HDV RNAs derived from genomic hairpin structures that mark the initiation sites of RNA-dependent HDV RNA transcription.

Subunit / interactions. Interacts with DICER1, AGO2, TARBP2, EIF6 and RPL7A (60S ribosome subunit); they form a large RNA-induced silencing complex (RISC). Interacts with APOBEC3G in an RNA-dependent manner. Interacts with TRIM71 (via NHL repeats) in an RNA-dependent manner. Interacts with both protein products of LIRE1, ORF1p and ORF2p. Interacts with TUT4 and, to a lesser extent, TUT7; the interactions are RNA-dependent. Interacts with AGO2, TNRC6B and UPF1; the interactions are direct and RNA-dependent. Interacts with FMR1; this interaction is direct, occurs in an RNA-dependent manner on polysomes and induces association of MOV10 with RNAs. Interacts with SHFL; the interaction increases in presence of RNA. Interacts with DHX34; the interaction is RNA-independent. Interacts with IKBKE. Interacts with RBM46. (Microbial infection) Interacts with the human hepatitis delta virus (HDV) antigen HDAg. (Microbial infection) Interacts with HIV-1 protein GAG.

Subcellular location. Cytoplasm. P-body. Cytoplasmic ribonucleoprotein granule. Stress granule. Nucleus.

Post-translational modifications. Ubiquitinated by the DCX(DCAF12) complex that specifically recognizes the glutamate-leucine (Glu-Leu) degron at the C-terminus, leading to its degradation. (Microbial infection) Cleaved and targeted for degradation by picornavirus proteases.

Induction. By herpes simplex 1/HHV-1 virus infection.

Similarity. Belongs to the DNA2/NAM7 helicase family. SDE3 subfamily.

Isoforms (3)

UniProt IDNamesCanonical?
Q9HCE1-11yes
Q9HCE1-22
Q9HCE1-33

RefSeq proteins (7): NP_001123551, NP_001273001, NP_001308253, NP_001356436, NP_001376491, NP_001376492, NP_066014 (=MANE)

Domains & families (InterPro)

IDNameType
IPR026122MOV-10/SDE3_DEXXQ/H-boxDomain
IPR027417P-loop_NTPaseHomologous_superfamily
IPR041677DNA2/NAM7_AAA_11Domain
IPR041679DNA2/NAM7-like_CDomain
IPR047187SF1_C_Upf1Domain
IPR049075MOV-10_NDomain
IPR049077MOV-10_Ig-likeDomain
IPR049079Mov-10_helicalDomain
IPR049080MOV-10-like_beta-barrelDomain

Pfam: PF13086, PF13087, PF21632, PF21633, PF21634, PF21635

Catalyzed reactions (Rhea), 1 shown:

  • ATP + H2O = ADP + phosphate + H(+) (RHEA:13065)

UniProt features (26 total): mutagenesis site 7, modified residue 6, splice variant 4, sequence conflict 3, region of interest 2, chain 1, short sequence motif 1, compositionally biased region 1, binding site 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9HCE1-F181.190.39

Functional residue map

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

Ligand- & substrate-binding residues (1): 524–531

Post-translational modifications (6): 969, 977, 148, 160, 254, 432

Mutagenesis-validated functional residues (7):

PositionPhenotype
129about 70% more antiviral activity against encephalomyocarditis virus replication; when associated with a-869.
530abolishes 5’ to 3’ directional unwinding activity. abolishes inhibition of rna chaperonne activity of lire1. no effect o
530attenuated anti-hbv activity.
645abolishes 5’ to 3’ directional unwinding activity.
646almost complete loss of the ability to prevent the degradation of apobec3g mediated by hiv-1 vif. attenuated anti-hbv ac
869about 70% more antiviral activity against encephalomyocarditis virus replication; when associated with a-129.
1002loss of interaction with dcaf12 and proteasomal degradation.

Function

Pathways and Gene Ontology

Reactome pathways

61 pathways

IDPathway
R-HSA-165159MTOR signalling
R-HSA-1912408Pre-NOTCH Transcription and Translation
R-HSA-2559580Oxidative Stress Induced Senescence
R-HSA-2559585Oncogene Induced Senescence
R-HSA-4086398Ca2+ pathway
R-HSA-5628897TP53 Regulates Metabolic Genes
R-HSA-5687128MAPK6/MAPK4 signaling
R-HSA-8853884Transcriptional Regulation by VENTX
R-HSA-8934593Regulation of RUNX1 Expression and Activity
R-HSA-8936459RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
R-HSA-8943723Regulation of PTEN mRNA translation
R-HSA-8948700Competing endogenous RNAs (ceRNAs) regulate PTEN translation
R-HSA-8986944Transcriptional Regulation by MECP2
R-HSA-9018519Estrogen-dependent gene expression
R-HSA-9022692Regulation of MECP2 expression and activity
R-HSA-9029569NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux
R-HSA-9725371Nuclear events stimulated by ALK signaling in cancer
R-HSA-9759811Regulation of CDH11 mRNA translation by microRNAs
R-HSA-9764562Regulation of CDH1 mRNA translation by microRNAs
R-HSA-9768778Regulation of NPAS4 mRNA translation
R-HSA-9824594Regulation of MITF-M-dependent genes involved in apoptosis
R-HSA-9839394TGFBR3 expression
R-HSA-9909620Regulation of PD-L1(CD274) translation
R-HSA-1257604PIP3 activates AKT signaling
R-HSA-1266738Developmental Biology
R-HSA-1500931Cell-Cell communication
R-HSA-157118Signaling by NOTCH
R-HSA-162582Signal Transduction
R-HSA-1643685Disease
R-HSA-1912422Pre-NOTCH Expression and Processing

MSigDB gene sets: 0 (showing top):

GO Biological Process (10): transposable element silencing (GO:0010526), regulatory ncRNA-mediated post-transcriptional gene silencing (GO:0035194), miRNA-mediated post-transcriptional gene silencing (GO:0035195), miRNA-mediated gene silencing by mRNA destabilization (GO:0035279), defense response to virus (GO:0051607), positive regulation of mRNA catabolic process (GO:0061014), 3’-UTR-mediated mRNA destabilization (GO:0061158), transposable element silencing by mRNA destabilization (GO:0141008), regulation of neuron projection arborization (GO:0150011), regulatory ncRNA-mediated gene silencing (GO:0031047)

GO Molecular Function (9): RNA binding (GO:0003723), ATP binding (GO:0005524), ATP hydrolysis activity (GO:0016887), 5’-3’ RNA helicase activity (GO:0032574), nucleotide binding (GO:0000166), RNA helicase activity (GO:0003724), helicase activity (GO:0004386), protein binding (GO:0005515), hydrolase activity (GO:0016787)

GO Cellular Component (8): P-body (GO:0000932), obsolete extracellular space (GO:0005615), nucleus (GO:0005634), cytosol (GO:0005829), cytoplasmic stress granule (GO:0010494), cytoplasmic ribonucleoprotein granule (GO:0036464), P granule (GO:0043186), cytoplasm (GO:0005737)

Reactome top-level categories

Rollup of top-17 pathways:

CategoryPathways
Cellular Senescence2
Generic Transcription Pathway2
Transcriptional regulation by RUNX12
Signal Transduction1
Pre-NOTCH Expression and Processing1
Beta-catenin independent WNT signaling1
Transcriptional Regulation by TP531
MAPK family signaling cascades1
PTEN Regulation1
Regulation of PTEN mRNA translation1
ESR-mediated signaling1
Transcriptional Regulation by MECP21
NR1H2 and NR1H3-mediated signaling1
Signaling by ALK fusions and activated point mutants1
Regulation of CDH11 Expression and Function1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
mRNA destabilization3
cytoplasmic ribonucleoprotein granule3
negative regulation of gene expression2
ATP-dependent activity2
cytoplasm2
cellular anatomical structure2
retrotransposition1
post-transcriptional gene silencing1
regulatory ncRNA-mediated gene silencing1
regulatory ncRNA-mediated post-transcriptional gene silencing1
miRNA-mediated post-transcriptional gene silencing1
defense response1
response to virus1
mRNA catabolic process1
positive regulation of catabolic process1
regulation of mRNA catabolic process1
positive regulation of mRNA metabolic process1
transposable element silencing1
regulation of cell morphogenesis1
regulation of cell projection organization1
neuron projection arborization1
nucleic acid binding1
adenyl ribonucleotide binding1
purine ribonucleoside triphosphate binding1
ribonucleoside triphosphate phosphatase activity1
RNA helicase activity1
nucleoside phosphate binding1
heterocyclic compound binding1
helicase activity1
ATP-dependent activity, acting on RNA1
catalytic activity, acting on RNA1
nucleic acid conformation isomerase activity1
catalytic activity, acting on a nucleic acid1
binding1
catalytic activity1
intracellular membrane-bounded organelle1
ribonucleoprotein granule1
germ plasm1
intracellular anatomical structure1

Protein interactions and networks

STRING

2008 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MOV10AGO2Q9UKV8991
MOV10DICER1Q9UPY3991
MOV10TNRC6BQ9UPQ9978
MOV10AGO1Q9UL18968
MOV10FMR1Q06787875
MOV10PUM2Q8TB72870
MOV10EIF6P56537777
MOV10FXR2P51116759
MOV10FXR1P51114759
MOV10TNRC6AQ8NDV7747
MOV10APOBEC3GQ9HC16739
MOV10DHX9Q08211712
MOV10UPF1Q92900647
MOV10PABPC1P11940642
MOV10ELAVL1Q15717641

IntAct

331 interactions, top by confidence:

ABTypeScore
IFIT1IFIT3psi-mi:“MI:0914”(association)0.920
NMOV10psi-mi:“MI:0915”(physical association)0.910
MOV10Npsi-mi:“MI:0914”(association)0.910
MOV10Npsi-mi:“MI:0403”(colocalization)0.910
DDX21Npsi-mi:“MI:0914”(association)0.870
NSPIK3R2psi-mi:“MI:0914”(association)0.750
NHNRNPRpsi-mi:“MI:0914”(association)0.730
CFTRESYT2psi-mi:“MI:0914”(association)0.710
HLA-ATAPBPpsi-mi:“MI:0915”(physical association)0.690
MOV10CBX8psi-mi:“MI:0915”(physical association)0.680
MOV10CBX7psi-mi:“MI:0915”(physical association)0.680
MOV10CBX7psi-mi:“MI:0914”(association)0.680
MOV10CBX6psi-mi:“MI:0915”(physical association)0.670
H1-1RRP8psi-mi:“MI:0914”(association)0.640
NOP53RRP8psi-mi:“MI:0914”(association)0.640
IGF2BP1IGF2BP3psi-mi:“MI:0914”(association)0.640
MOV10BMI1psi-mi:“MI:0915”(physical association)0.620
CFTRHAX1psi-mi:“MI:0914”(association)0.610
MOV10Cbx7psi-mi:“MI:0407”(direct interaction)0.590
MOV10Cbx7psi-mi:“MI:0915”(physical association)0.590
MOV10IGF2BP1psi-mi:“MI:0915”(physical association)0.560

BioGRID (1482): NOC2L (Affinity Capture-RNA), AGRN (Affinity Capture-RNA), NADK (Affinity Capture-RNA), PGD (Affinity Capture-RNA), DFFA (Affinity Capture-RNA), SRM (Affinity Capture-RNA), EXOSC10 (Affinity Capture-RNA), MTOR (Affinity Capture-RNA), MAD2L2 (Affinity Capture-RNA), CLCN6 (Affinity Capture-RNA), SZRD1 (Affinity Capture-RNA), UBR4 (Affinity Capture-RNA), MINOS1 (Affinity Capture-RNA), DDOST (Affinity Capture-RNA), E2F2 (Affinity Capture-RNA)

ESM2 similar proteins: A0A8C2MDK8, A0A8I6GM68, A6H751, A7YY46, A8MX76, D3YXS5, D3ZBP4, D3ZEY4, E7F9T0, E9QAM5, F1MH07, F1QCV2, F8WLE0, P16452, P23249, P48760, P49222, P52824, Q2NKY8, Q2QWU2, Q3SYT1, Q3ZBE0, Q4R380, Q50L43, Q5BJS0, Q5NCQ5, Q5R607, Q5RKI3, Q5ZI74, Q69ZP3, Q6P5E8, Q6ZSI9, Q7L2E3, Q8BX80, Q8N490, Q8NFD2, Q8NFI3, Q8TDZ2, Q8TE96, Q8VDP3

Diamond homologs: B6SFA4, D3ZG52, E1BMP7, E9QAM5, F1RCY6, O76512, O94247, O94387, P23249, P30771, P32644, P38935, P40694, P51530, Q00416, Q09449, Q09820, Q0V8H6, Q0VGT4, Q1LXK4, Q54I89, Q57568, Q60560, Q86AS0, Q86YA3, Q8GYD9, Q8QHA5, Q8R151, Q92355, Q92900, Q98TR3, Q9BYK8, Q9EPU0, Q9EQN5, Q9FJR0, Q9HCE1, Q9HEH1, Q9P2E3, Q9VYS3, P39369

SIGNOR signaling

3 interactions.

AEffectBMechanism
Interferon-type-I“up-regulates quantity by expression”MOV10“transcriptional regulation”
MOV10“up-regulates activity”IKBKEbinding
MOV10“up-regulates activity”UPF1binding

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 203 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

Reactome pathways:

PathwayPartnersFoldFDR
SUMOylation of DNA methylation proteins525.8×7e-04
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known613.9×1e-03
SUMOylation of transcription cofactors611.2×1e-03
SUMOylation of RNA binding proteins611.0×1e-03
PTEN Regulation610.5×1e-03
Regulation of PTEN gene transcription79.6×1e-03
Signaling by ALK fusions and activated point mutants78.1×1e-03
Differentiation of naive CD4+ T cells to T helper 2 cells (Th2 cells)77.9×2e-03

GO biological processes:

GO termPartnersFoldFDR
positive regulation of viral genome replication516.3×2e-03
mRNA stabilization612.3×2e-03
negative regulation of translation1011.0×3e-05
mRNA export from nucleus610.0×5e-03
rRNA processing97.2×1e-03
translation116.3×6e-04
defense response to virus114.3×8e-03
protein phosphorylation114.2×9e-03

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance107
Likely benign9
Benign7

Top pathogenic / likely-pathogenic (0)

SpliceAI

3455 predictions. Top by Δscore:

VariantEffectΔscore
1:112689135:ACAG:Adonor_loss1.0000
1:112689137:AGGT:Adonor_loss1.0000
1:112689410:CCCA:Cacceptor_loss1.0000
1:112689413:A:AGacceptor_gain1.0000
1:112689413:AG:Aacceptor_gain1.0000
1:112689414:G:GAacceptor_loss1.0000
1:112689414:G:GGacceptor_gain1.0000
1:112689414:GG:Gacceptor_gain1.0000
1:112689414:GGGCT:Gacceptor_gain1.0000
1:112689651:GTGA:Gdonor_gain1.0000
1:112689653:GA:Gdonor_gain1.0000
1:112689655:G:GGdonor_gain1.0000
1:112689837:CAG:Cacceptor_loss1.0000
1:112689839:G:GCacceptor_loss1.0000
1:112689839:GGT:Gacceptor_gain1.0000
1:112690079:G:GTdonor_gain1.0000
1:112690080:A:Tdonor_gain1.0000
1:112690084:A:Tdonor_gain1.0000
1:112690099:G:GCdonor_loss1.0000
1:112690099:G:GGdonor_gain1.0000
1:112691654:C:CAacceptor_gain1.0000
1:112691663:A:AGacceptor_gain1.0000
1:112691663:AGC:Aacceptor_gain1.0000
1:112691664:G:GGacceptor_gain1.0000
1:112691664:GC:Gacceptor_gain1.0000
1:112691664:GCG:Gacceptor_gain1.0000
1:112691664:GCGCT:Gacceptor_gain1.0000
1:112691800:G:GGdonor_gain1.0000
1:112691801:TAA:Tdonor_loss1.0000
1:112692756:TCCA:Tacceptor_loss1.0000

AlphaMissense

6492 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
1:112696846:G:TR733M1.000
1:112694846:G:AG524R0.999
1:112694846:G:CG524R0.999
1:112694846:G:TG524W0.999
1:112694847:G:AG524E0.999
1:112694856:G:AG527D0.999
1:112694862:G:AG529D0.999
1:112694864:A:CK530Q0.999
1:112694865:A:TK530M0.999
1:112696490:A:CE646A0.999
1:112696490:A:TE646V0.999
1:112696687:A:GD680G0.999
1:112696687:A:TD680V0.999
1:112696697:G:CQ683H0.999
1:112696697:G:TQ683H0.999
1:112696841:C:AN731K0.999
1:112696841:C:GN731K0.999
1:112696846:G:CR733T0.999
1:112699793:T:CF898L0.999
1:112699794:T:CF898S0.999
1:112699795:C:AF898L0.999
1:112699795:C:GF898L0.999
1:112699902:T:AN906K0.999
1:112699902:T:GN906K0.999
1:112699906:G:CA908P0.999
1:112699907:C:AA908D0.999
1:112699975:T:AW931R0.999
1:112699975:T:CW931R0.999
1:112694855:G:CG527R0.998
1:112694865:A:CK530T0.998

dbSNP variants (sampled 300 via entrez): RS1000004804 (1:112687856 G>T), RS1000016671 (1:112692915 C>T), RS1000114216 (1:112701137 C>G,T), RS1000126367 (1:112684181 C>G), RS1000299807 (1:112672644 G>A,T), RS1000374387 (1:112678832 G>A), RS1000397557 (1:112697498 C>G,T), RS1000600476 (1:112689768 T>C), RS1000624231 (1:112673935 T>C), RS1000672184 (1:112691195 G>A,C), RS1000718736 (1:112674197 C>G,T), RS1000728476 (1:112695961 G>A), RS1001400727 (1:112699154 C>T), RS1001748870 (1:112673618 C>T), RS1001827950 (1:112691921 C>G,T)

Disease associations

OMIM: gene MIM:610742 | disease phenotypes:

GenCC curated gene-disease

Mondo (1): primary ovarian failure (MONDO:0005387)

Orphanet (1): NON RARE IN EUROPE: Primary ovarian failure (Orphanet:619)

HPO phenotypes

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

GWAS associations

44 associations (top):

StudyTraitp-value
GCST001227_19Systolic blood pressure1.000000e-09
GCST001228_13Diastolic blood pressure1.000000e-09
GCST001236_18Blood pressure8.000000e-06
GCST001238_5Hypertension3.000000e-07
GCST002627_6Hypertension3.000000e-09
GCST002630_7Systolic blood pressure3.000000e-09
GCST002631_11Diastolic blood pressure8.000000e-08
GCST004067_194Hip circumference adjusted for BMI9.000000e-07
GCST004067_82Hip circumference adjusted for BMI6.000000e-09
GCST004776_10Systolic blood pressure2.000000e-07
GCST004777_31Diastolic blood pressure1.000000e-10
GCST004777_46Diastolic blood pressure2.000000e-08
GCST004777_60Diastolic blood pressure6.000000e-19
GCST006166_108Diastolic blood pressure x alcohol consumption interaction (2df test)5.000000e-20
GCST006167_20Mean arterial pressure x alcohol consumption interaction (2df test)1.000000e-09
GCST006258_50Diastolic blood pressure9.000000e-10
GCST006259_26Systolic blood pressure1.000000e-12
GCST006434_57Systolic blood pressure x alcohol consumption interaction (2df test)2.000000e-14
GCST007094_48Diastolic blood pressure7.000000e-12
GCST007099_168Systolic blood pressure3.000000e-07
GCST007294_13Body fat distribution (trunk fat ratio)9.000000e-19
GCST007294_32Body fat distribution (trunk fat ratio)1.000000e-08
GCST007295_163Body fat distribution (leg fat ratio)8.000000e-07
GCST007295_7Body fat distribution (leg fat ratio)7.000000e-16
GCST007703_106Systolic blood pressure1.000000e-11
GCST007704_13Diastolic blood pressure4.000000e-10
GCST007706_47Mean arterial pressure3.000000e-12
GCST007707_93Hypertension3.000000e-13
GCST007928_55Medication use (diuretics)1.000000e-12
GCST008839_75Height2.000000e-15

EFO canonical traits (13, from GWAS)

EFO IDTrait name
EFO:0006335systolic blood pressure
EFO:0006336diastolic blood pressure
EFO:0006340mean arterial pressure
EFO:0008039BMI-adjusted hip circumference
EFO:0004329alcohol drinking
EFO:0004341body fat distribution
EFO:0009928Diuretic use measurement
EFO:0004771visual cortical surface area measurement
EFO:0004346neuroimaging measurement
EFO:0004840cortical thickness
EFO:0009819comparative body size at age 10, self-reported
EFO:0007985platelet crit
EFO:0004309platelet count

MeSH disease descriptors (1)

DescriptorNameTree numbers
D016649Primary Ovarian InsufficiencyC12.050.351.500.056.630.750; C12.100.250.056.630.750; C19.391.630.750

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

PharmGKB variants

2 variants.

VariantGenesLevelScore#Clin annotsDrugs
rs2932538MOV100.000
rs12069113CAPZA1, MOV100.000

CTD chemical–gene interactions

47 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects cotreatment, decreases expression, affects expression, decreases methylation7
trichostatin Aaffects cotreatment, decreases expression3
bisphenol Aincreases abundance, decreases expression, increases expression, decreases reaction2
methacrylaldehydeincreases abundance, affects cotreatment, increases expression2
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression2
Acroleinaffects cotreatment, increases expression, increases abundance2
Cisplatinincreases expression, affects cotreatment2
Ozoneaffects cotreatment, increases expression, increases abundance2
Cyclosporinedecreases expression2
Aflatoxin B1decreases methylation, increases methylation2
aristolochic acid Idecreases expression1
FR900359decreases phosphorylation1
ginger extractdecreases reaction, increases abundance, increases expression1
alpha-pineneaffects cotreatment, increases expression, increases abundance1
decabromobiphenyl etherdecreases expression1
sodium arsenitedecreases expression1
cobaltous chloridedecreases expression1
butyraldehydedecreases expression1
benzo(e)pyreneincreases methylation1
potassium chromate(VI)affects cotreatment, decreases expression1
M-VAC protocoldecreases response to substance1
epigallocatechin gallateaffects cotreatment, decreases expression1
pentanaldecreases expression1
CGP 52608affects binding, increases reaction1
JP8 aviation fueldecreases expression1
dorsomorphindecreases expression, affects cotreatment1
jinfukangaffects cotreatment, increases expression1
LDN 193189affects cotreatment, decreases expression1
(+)-JQ1 compounddecreases expression1
Sunitinibdecreases expression1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT00417066PHASE4COMPLETEDFlexible GnRH Antagonist vs Flare up GnRH Agonist Protocol in Poor Responders
NCT00732693PHASE4COMPLETEDEvaluation of Physiologic and Standard Sex Steroid Replacement Regimens in Women With Premature Ovarian Failure
NCT00837616PHASE4COMPLETEDEstrogen Dosing in Turner Syndrome: Pharmacology and Metabolism
NCT01853501PHASE4UNKNOWNEffects of ADSC Therapy in Women With POF
NCT02783937PHASE4COMPLETEDFilgrastim for Premature Ovarian Insufficiency
NCT03535480PHASE4UNKNOWNAutologous Bone Marrow Stem Cell Ovarian Transplantation to Restore Ovarian Function in Premature Ovarian Failure
NCT00140998PHASE3COMPLETEDEstrogen Treatment (Oral vs. Patches) in Turner Syndrome
NCT00001951PHASE2COMPLETEDHormone Replacement in Young Women With Premature Ovarian Failure
NCT00370019PHASE2WITHDRAWNEffects of an Estrogen Replacement Therapy Skin Patch on Ovulation in Women With Premature Ovarian Failure
NCT00429494PHASE2COMPLETEDGnRH Analogue for Ovarian Function Preservation in Hematopoietic Stem Cell Transplantation Patients
NCT03816852PHASE2SUSPENDEDThe Safety and Efficiency Study of Mesenchymal Stem Cell (19#iSCLife®-POI) in Premature Ovarian Insufficiency
NCT04536467PHASE2UNKNOWNPrevention of Chemotherapy-Induced Ovarian Failure With Goserelin in Premenopausal Lymphoma Patients
NCT06117982PHASE2COMPLETEDThe Impact of Granulocyte Colony Stimulating Factor on Premature Ovarian Insufficiency
NCT02912104PHASE1COMPLETEDA Therapeutic Trial of Human Amniotic Epithelial Cells Transplantation for Primary Ovarian Failure
NCT03178695PHASE1COMPLETEDInovium Ovarian Rejuvenation Trials
NCT04815213PHASE1ACTIVE_NOT_RECRUITINGThe Use of Expandeded Mesenchymal Stromal Cells (MSC) in Premature Ovarian Failure (POF) in Adult Humans
NCT05138367PHASE1COMPLETEDEffects of UCA-PSCs in Women With POF
NCT06132542PHASE1UNKNOWNAutologous ADMSC Transplantation in Patients With POI
NCT00948857PHASE2/PHASE3TERMINATEDDehydroepiandrosterone (DHEA) Treatment and Premature Ovarian Failure (POF)
NCT04031456PHASE2/PHASE3RECRUITINGAutologous PRP Infusion May Restore Ovarian Function and May Promote Folliculogenesis in POI Patients
NCT02043743PHASE1/PHASE2UNKNOWNAutologous Stem Cells Transplantation in Patients With Idiopathic and Drug Induced Premature Ovarian Failure
NCT02062931PHASE1/PHASE2UNKNOWNAutologous Mesenchymal Stem Cells Transplantation In Women With Premature Ovarian Failure
NCT02151890PHASE1/PHASE2COMPLETEDPregnancy After Stem Cell Transplantation in Premature Ovarian Failure
NCT02372474PHASE1/PHASE2COMPLETEDIt is a Real The First Baby Of Autologous Stem Cell Therapy in Premature Ovarian Failure
NCT02603744PHASE1/PHASE2UNKNOWNAutologous Adipose Derived Mesenchymal Stromal Cells Transplantation in Women With Premature Ovarian Failure (POF)
NCT02644447PHASE1/PHASE2COMPLETEDTransplantation of HUC-MSCs With Injectable Collagen Scaffold for POF
NCT03069209PHASE1/PHASE2UNKNOWNAutologous Bone Marrow-Derived Stem Cell Transplantation in Patients With Premature Ovarian Failure (POF)
NCT03985462PHASE1/PHASE2WITHDRAWNVery Small Embryonic-like Stem Cells for Ovary
NCT04009473PHASE1/PHASE2UNKNOWNStem Cell Therapy and Growth Factor Ovarian in Vitro Activation
NCT04071574PHASE1/PHASE2COMPLETEDComparative Study on the Efficacy of Ovarian Stimulation Protocols on the Success Rate of ICSI in Female Infertility
NCT04922398PHASE1/PHASE2UNKNOWNOvarian Injection of PRP (Platelet -Rich Plasma) Vs Normal Saline in Premature Ovarian Insufficiency
NCT05462379PHASE1/PHASE2ACTIVE_NOT_RECRUITINGAutologous Heterotopic Fresh Ovarian Graft in Woman With LACC Eligible for Pelvic Radiotherapy Treatment.
NCT06202547PHASE1/PHASE2UNKNOWNIntra-ovarian Injection of MSC-EVs in Idiopathic Premature Ovarian Failure
NCT01129947EARLY_PHASE1WITHDRAWNThe Use of DHEA in Women With Premature Ovarian Failure
NCT05522634EARLY_PHASE1UNKNOWNA Clinical Study of Chinese Herbal Compound TJAOA101 in the Treatment of Premature Ovarian Insufficiency
NCT07308327EARLY_PHASE1ACTIVE_NOT_RECRUITINGThe Influence of Gut Microbiota on Ovarian Function: A Single-center, Randomized,Double Blind, Parallel-controlled, Exploratory Clinical Trial
NCT00001275Not specifiedCOMPLETEDOvarian Follicle Function in Patients With Primary Ovarian Failure
NCT00001306Not specifiedCOMPLETEDSteroid Therapy in Autoimmune Premature Ovarian Failure
NCT00006156Not specifiedCOMPLETEDFeasibility Study for Development of an Early Test for Ovarian Failure
NCT00119925Not specifiedUNKNOWN‘SPRING’-Study: Subfertility Guidelines: Patient Related Implementation in the Netherlands Among Gynaecologists

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