MORN2

gene
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Also known as MOPT

Summary

MORN2 (MORN repeat containing 2, HGNC:30166) is a protein-coding gene on chromosome 2p22.1, encoding MORN repeat-containing protein 2 (Q502X0). Might have a role in spermatogenesis.

Predicted to be involved in cell differentiation and spermatogenesis. Predicted to be located in acrosomal vesicle and nucleus.

Source: NCBI Gene 729967 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 16 total
  • MANE Select transcript: NM_001145450

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:30166
Approved symbolMORN2
NameMORN repeat containing 2
Location2p22.1
Locus typegene with protein product
StatusApproved
AliasesMOPT
Ensembl geneENSG00000188010
Ensembl biotypeprotein_coding
Entrez729967

Gene structure

Transcript identifiers

Ensembl transcripts: 5 — 5 protein_coding

ENST00000409077, ENST00000409131, ENST00000409665, ENST00000410014, ENST00000644631

RefSeq mRNA: 1 — MANE Select: NM_001145450 NM_001145450

CCDS: CCDS46262

Canonical transcript exons

ENST00000644631 — 5 exons

ExonStartEnd
ENSE000013760233888241338882709
ENSE000013844483888144238881578
ENSE000017088013887597638876110
ENSE000038166193888017938880229
ENSE000038190453888060038880706

Expression profiles

Bgee: expression breadth ubiquitous, 240 present calls, max score 98.85.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 26.6228 / max 531.8351, expressed in 1793 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1984126.62281793

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
left testisUBERON:000453398.85gold quality
right testisUBERON:000453498.71gold quality
right uterine tubeUBERON:000130298.66gold quality
bronchial epithelial cellCL:000232898.44gold quality
olfactory segment of nasal mucosaUBERON:000538698.36gold quality
bronchusUBERON:000218598.00gold quality
testisUBERON:000047397.27gold quality
adenohypophysisUBERON:000219695.62gold quality
pituitary glandUBERON:000000795.21gold quality
caudate nucleusUBERON:000187394.73gold quality
nucleus accumbensUBERON:000188294.57gold quality
putamenUBERON:000187494.07gold quality
hypothalamusUBERON:000189894.03gold quality
mucosa of paranasal sinusUBERON:000503094.00gold quality
anterior cingulate cortexUBERON:000983593.54gold quality
adult mammalian kidneyUBERON:000008293.49gold quality
adult organismUBERON:000702393.39gold quality
amygdalaUBERON:000187693.23gold quality
spermCL:000001992.92gold quality
islet of LangerhansUBERON:000000692.79gold quality
left lobe of thyroid glandUBERON:000112092.44gold quality
right adrenal gland cortexUBERON:003582792.40gold quality
C1 segment of cervical spinal cordUBERON:000646992.21gold quality
right adrenal glandUBERON:000123392.08gold quality
prefrontal cortexUBERON:000045192.02gold quality
right frontal lobeUBERON:000281092.02gold quality
thyroid glandUBERON:000204691.83gold quality
left adrenal glandUBERON:000123491.79gold quality
left adrenal gland cortexUBERON:003582591.75gold quality
Brodmann (1909) area 9UBERON:001354091.59gold quality

Single-cell (SCXA)

Detected in 10 experiment(s), a significant marker in 8.

ExperimentMarker?Max mean expression
E-CURD-114yes1581.91
E-MTAB-6701yes626.15
E-HCAD-1yes32.86
E-GEOD-134144yes30.79
E-MTAB-10287yes27.94
E-GEOD-130148yes13.51
E-MTAB-9388yes7.46
E-CURD-10no173.78
E-GEOD-99795no89.20
E-ANND-3no0.00

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • MOPT is associated with dynamic regulation of acrosome biogenesis during late spermiogenesis. (PMID:19913896)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriomorn2ENSDARG00000071360
mus_musculusMorn2ENSMUSG00000045257
rattus_norvegicusENSRNOG00000082556

Paralogs (7): MORN1 (ENSG00000116151), MORN3 (ENSG00000139714), SETD7 (ENSG00000145391), RSPH10B (ENSG00000155026), RSPH1 (ENSG00000160188), RSPH10B2 (ENSG00000169402), ALS2CL (ENSG00000178038)

Protein

Protein identifiers

MORN repeat-containing protein 2Q502X0 (reviewed: Q502X0)

Alternative names: MORN motif protein in testis

All UniProt accessions (4): Q502X0, A0A2R8YE86, B8ZZ40, B8ZZN7

UniProt curated annotations — full annotation on UniProt →

Function. Might have a role in spermatogenesis.

Subcellular location. Cytoplasmic vesicle. Secretory vesicle. Acrosome. Nucleus.

RefSeq proteins (1): NP_001138922* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR003409MORNRepeat
IPR052849MORN_repeat_proteinFamily

Pfam: PF02493

UniProt features (4 total): repeat 2, chain 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q502X0-F191.470.79

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 87 (showing top): CCAWYNNGAAR_UNKNOWN, GOCC_SECRETORY_GRANULE, CHIANG_LIVER_CANCER_SUBCLASS_UNANNOTATED_DN, GOBP_MALE_GAMETE_GENERATION, SENGUPTA_NASOPHARYNGEAL_CARCINOMA_DN, GOBP_DEVELOPMENTAL_PROCESS_INVOLVED_IN_REPRODUCTION, RFX1_02, ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, CUI_TCF21_TARGETS_2_UP, GOCC_SECRETORY_VESICLE, GOCC_ACROSOMAL_VESICLE, SCGGAAGY_ELK1_02, DODD_NASOPHARYNGEAL_CARCINOMA_DN, KRIGE_RESPONSE_TO_TOSEDOSTAT_6HR_DN, chr2p22

GO Biological Process (2): spermatogenesis (GO:0007283), cell differentiation (GO:0030154)

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (3): acrosomal vesicle (GO:0001669), nucleus (GO:0005634), cytoplasmic vesicle (GO:0031410)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
developmental process involved in reproduction1
male gamete generation1
cellular developmental process1
binding1
secretory granule1
intracellular membrane-bounded organelle1
cytoplasm1
intracellular vesicle1

Protein interactions and networks

STRING

228 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MORN2C11orf97A0A1B0GVM6693
MORN2TMEM239Q8WW34506
MORN2MORN4Q8NDC4435
MORN2ARHGEF33A8MVX0433
MORN2ANKRD35Q8N283404
MORN2DHX57Q6P158392
MORN2MORN3Q6PF18378
MORN2CNBD2Q96M20370
MORN2THSD1Q9NS62350
MORN2AIRIMQ9NX04348
MORN2IQCF1Q8N6M8325
MORN2PPP1R37O75864323
MORN2CDKL4Q5MAI5296
MORN2ZNF358Q9NW07288
MORN2RAPGEF5Q92565284

IntAct

11 interactions, top by confidence:

ABTypeScore
CCDC120AIPpsi-mi:“MI:0914”(association)0.640
GORASP2MORN2psi-mi:“MI:0915”(physical association)0.560
MORN2GORASP2psi-mi:“MI:0915”(physical association)0.560
C8orf74FGFR2psi-mi:“MI:0914”(association)0.530
RSPH1MORN2psi-mi:“MI:0915”(physical association)0.000
MPP3MORN2psi-mi:“MI:0915”(physical association)0.000

BioGRID (8): MORN2 (Two-hybrid), MORN2 (Affinity Capture-MS), MORN2 (Synthetic Growth Defect), MORN2 (Affinity Capture-MS), MORN2 (Affinity Capture-MS), MORN2 (Affinity Capture-MS), MORN2 (Affinity Capture-MS), MORN2 (Two-hybrid)

ESM2 similar proteins: B6CZ17, B6CZ18, O00423, P10830, P53671, Q05BC3, Q08CH7, Q09537, Q15326, Q1XHL7, Q21029, Q28FE4, Q32KM6, Q32KU3, Q32LL6, Q49HM9, Q4R3N2, Q4R842, Q4V8C3, Q4VBJ9, Q502X0, Q569C2, Q5PPV3, Q5TYQ3, Q5VZ52, Q5ZIJ9, Q622Z7, Q63651, Q641X6, Q6GNY1, Q6IND7, Q6PF18, Q6VTH5, Q7DMA9, Q7Z0G7, Q804S5, Q80SY4, Q86YT6, Q8C5T4, Q8K4M9

Diamond homologs: Q32KU3, Q502X0, Q6UL01

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance7
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

446 predictions. Top by Δscore:

VariantEffectΔscore
2:38876106:GCCAA:Gdonor_gain1.0000
2:38876111:G:GGdonor_gain1.0000
2:38880172:A:AGacceptor_gain1.0000
2:38880596:TTAG:Tacceptor_loss1.0000
2:38880598:A:AGacceptor_gain1.0000
2:38880598:AGAT:Aacceptor_gain1.0000
2:38880599:G:GAacceptor_gain1.0000
2:38880599:G:GCacceptor_loss1.0000
2:38880599:GA:Gacceptor_gain1.0000
2:38880599:GAT:Gacceptor_gain1.0000
2:38880599:GATG:Gacceptor_gain1.0000
2:38880687:G:GTdonor_gain1.0000
2:38880695:A:Tdonor_gain1.0000
2:38880702:ACAAG:Adonor_loss1.0000
2:38880704:AAGG:Adonor_loss1.0000
2:38880705:AGGTA:Adonor_loss1.0000
2:38880706:GG:Gdonor_loss1.0000
2:38880707:G:Cdonor_loss1.0000
2:38880708:T:Adonor_loss1.0000
2:38881436:A:AGacceptor_gain1.0000
2:38881437:AACAG:Aacceptor_loss1.0000
2:38881438:ACAGA:Aacceptor_loss1.0000
2:38881439:CAGAT:Cacceptor_loss1.0000
2:38881440:A:AGacceptor_gain1.0000
2:38881440:A:Cacceptor_loss1.0000
2:38881441:G:Aacceptor_loss1.0000
2:38881441:G:GGacceptor_gain1.0000
2:38881441:GAT:Gacceptor_gain1.0000
2:38881441:GATGA:Gacceptor_gain1.0000
2:38880173:A:Gacceptor_gain0.9900

AlphaMissense

1001 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
2:38881523:G:TG28W0.989
2:38881529:T:GY30D0.989
2:38881560:G:AG40E0.989
2:38882432:T:GY53D0.989
2:38881553:T:GY38D0.988
2:38881565:T:CF42L0.986
2:38881567:C:AF42L0.986
2:38881567:C:GF42L0.986
2:38881497:T:CF19S0.984
2:38881560:G:TG40V0.984
2:38881484:T:GY15D0.983
2:38881491:G:AG17E0.983
2:38881566:T:CF42S0.983
2:38881496:T:CF19L0.981
2:38881498:T:AF19L0.981
2:38881498:T:GF19L0.981
2:38881461:T:CL7P0.979
2:38881491:G:TG17V0.979
2:38881490:G:AG17R0.978
2:38881490:G:CG17R0.978
2:38881518:G:TG26V0.976
2:38881524:G:AG28E0.976
2:38882426:G:TG51W0.975
2:38882468:T:CF65L0.974
2:38882470:T:AF65L0.974
2:38882470:T:GF65L0.974
2:38881559:G:AG40R0.972
2:38881559:G:CG40R0.972
2:38881523:G:AG28R0.971
2:38881523:G:CG28R0.971

dbSNP variants (sampled 300 via entrez): RS1000149694 (2:38880036 G>A,T), RS1000520205 (2:38878372 T>C), RS1000568303 (2:38882240 G>A,T), RS1000987807 (2:38874064 A>T), RS1001005568 (2:38880200 G>A,C), RS1001151622 (2:38878724 C>T), RS1001613764 (2:38874380 T>C), RS1002270976 (2:38878290 C>G), RS1003015825 (2:38882610 A>G), RS1003273766 (2:38882339 T>C), RS1003302099 (2:38877087 C>T), RS1003436143 (2:38878260 C>G), RS1003503492 (2:38882631 A>C), RS1004155648 (2:38875492 C>A), RS1004423752 (2:38874327 G>C)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
Air Pollutantsaffects cotreatment, increases abundance, increases expression, decreases expression4
Valproic Acidaffects expression, increases expression3
bisphenol Adecreases expression, increases expression2
Smokedecreases expression, increases abundance, increases expression2
dicrotophosdecreases expression1
methylmercuric chloridedecreases expression1
alpha-pineneaffects cotreatment, increases expression, increases abundance1
arseniteaffects binding, increases reaction1
sodium arseniteincreases abundance, increases expression1
manganese chlorideincreases abundance, increases expression1
methacrylaldehydeincreases abundance, affects cotreatment, increases expression1
CGP 52608affects binding, increases reaction1
deguelindecreases expression1
K 7174decreases expression1
fenpyroximatedecreases expression1
4-chloro-N-((4-(1,1-dimethylethyl)phenyl)methyl)-3-ethyl-1-methyl-1H-pyrazole-5-carboxamidedecreases expression1
pyrimidifendecreases expression1
Resveratrolaffects cotreatment, increases expression1
Acroleinaffects cotreatment, increases expression, increases abundance1
Antimycin Adecreases expression1
Arsenicincreases abundance, increases expression1
Coalincreases abundance, decreases expression1
Estradioldecreases expression1
Ethyl Methanesulfonateincreases expression1
Formaldehydeincreases expression1
Manganeseincreases abundance, increases expression1
Methyl Methanesulfonateincreases expression1
Ozoneaffects cotreatment, increases expression, increases abundance1
Plant Extractsincreases expression, affects cotreatment1
Quercetindecreases 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.