MORN5

gene
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Also known as FLJ46909

Summary

MORN5 (MORN repeat containing 5, HGNC:17841) is a protein-coding gene on chromosome 9q33.2, encoding MORN repeat-containing protein 5 (Q5VZ52).

Predicted to be located in sperm flagellum.

Source: NCBI Gene 254956 — RefSeq curated summary.

At a glance

  • Gene–disease (curated): isolated cleft palate (No Known Disease Relationship, GenCC)
  • GWAS associations: 3
  • Clinical variants (ClinVar): 31 total
  • MANE Select transcript: NM_198469

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:17841
Approved symbolMORN5
NameMORN repeat containing 5
Location9q33.2
Locus typegene with protein product
StatusApproved
AliasesFLJ46909
Ensembl geneENSG00000185681
Ensembl biotypeprotein_coding
OMIM619837
Entrez254956

Gene structure

Transcript identifiers

Ensembl transcripts: 6 — 4 protein_coding, 2 protein_coding_CDS_not_defined

ENST00000373764, ENST00000418632, ENST00000477017, ENST00000486801, ENST00000536616, ENST00000918677

RefSeq mRNA: 2 — MANE Select: NM_198469 NM_001286828, NM_198469

CCDS: CCDS6836, CCDS75894

Canonical transcript exons

ENST00000373764 — 5 exons

ExonStartEnd
ENSE00001302917122169645122169756
ENSE00001461480122199885122200083
ENSE00002213915122159908122160019
ENSE00003508038122174496122174627
ENSE00003666188122166768122166915

Expression profiles

Bgee: expression breadth ubiquitous, 159 present calls, max score 99.02.

FANTOM5 (CAGE): breadth broad, TPM avg 0.7191 / max 138.9342, expressed in 201 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
983990.6743192
984000.044818

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bronchial epithelial cellCL:000232899.02gold quality
right uterine tubeUBERON:000130298.42gold quality
bronchusUBERON:000218598.02gold quality
left testisUBERON:000453395.84gold quality
right testisUBERON:000453495.71gold quality
olfactory segment of nasal mucosaUBERON:000538694.29gold quality
testisUBERON:000047392.94gold quality
muscle layer of sigmoid colonUBERON:003580591.57gold quality
mucosa of paranasal sinusUBERON:000503091.47gold quality
smooth muscle tissueUBERON:000113591.45gold quality
adult organismUBERON:000702389.64gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047389.26gold quality
fallopian tubeUBERON:000388987.97gold quality
spermCL:000001986.07gold quality
epithelium of nasopharynxUBERON:000195183.57gold quality
oviduct epitheliumUBERON:000480483.47gold quality
left uterine tubeUBERON:000130380.59gold quality
pancreatic ductal cellCL:000207976.61silver quality
nasal cavity epitheliumUBERON:000538476.12silver quality
body of uterusUBERON:000985375.33gold quality
hypothalamusUBERON:000189874.01gold quality
caudate nucleusUBERON:000187373.88gold quality
nasal cavity mucosaUBERON:000182673.65gold quality
right lungUBERON:000216773.28gold quality
lower esophagusUBERON:001347372.52gold quality
lower esophagus muscularis layerUBERON:003583372.51gold quality
nucleus accumbensUBERON:000188272.45gold quality
myometriumUBERON:000129672.27gold quality
tracheaUBERON:000312672.13gold quality
caput epididymisUBERON:000435872.11gold quality

Single-cell (SCXA)

Detected in 4 experiment(s), a significant marker in 4.

ExperimentMarker?Max mean expression
E-CURD-114yes62.62
E-HCAD-1yes30.43
E-MTAB-10287yes26.33
E-ANND-3no0.00

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

9 targeting MORN5, 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-120099.7170.421838
HSA-MIR-442498.9170.331145
HSA-MIR-4436B-3P98.2565.261494
HSA-MIR-6735-5P98.2465.361488
HSA-MIR-7843-5P98.1265.261421
HSA-MIR-4632-5P97.8265.381470
HSA-MIR-6879-5P97.7765.521521
HSA-MIR-445697.5064.881678
HSA-MIR-797396.4865.54502

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriomorn5ENSDARG00000033610
mus_musculusMorn5ENSMUSG00000026894
rattus_norvegicusMorn5ENSRNOG00000026111

Protein

Protein identifiers

MORN repeat-containing protein 5Q5VZ52 (reviewed: Q5VZ52)

All UniProt accessions (3): A0A0A0MTF6, Q5VZ52, Q5T7S4

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Cell projection. Cilium. Flagellum.

Tissue specificity. Expressed in sperm (at protein level).

Isoforms (2)

UniProt IDNamesCanonical?
Q5VZ52-11yes
Q5VZ52-22

RefSeq proteins (2): NP_001273757, NP_940871* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR003409MORNRepeat
IPR042814Morn5Family

Pfam: PF02493

UniProt features (6 total): repeat 3, chain 1, splice variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q5VZ52-F191.190.69

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 50 (showing top): DARWICHE_SKIN_TUMOR_PROMOTER_DN, DARWICHE_PAPILLOMA_RISK_LOW_DN, DARWICHE_PAPILLOMA_RISK_HIGH_UP, DARWICHE_SQUAMOUS_CELL_CARCINOMA_UP, DARWICHE_PAPILLOMA_PROGRESSION_RISK, SENGUPTA_NASOPHARYNGEAL_CARCINOMA_DN, GOCC_MOTILE_CILIUM, GOCC_CILIUM, DODD_NASOPHARYNGEAL_CARCINOMA_DN, BRUINS_UVC_RESPONSE_VIA_TP53_GROUP_B, GOCC_9PLUS2_MOTILE_CILIUM, CBX5_TARGET_GENES, HMG20B_TARGET_GENES, NPAT_TARGET_GENES, TEAD2_TARGET_GENES

GO Biological Process (0):

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

GO Cellular Component (4): sperm flagellum (GO:0036126), cilium (GO:0005929), motile cilium (GO:0031514), cell projection (GO:0042995)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding1
9+2 motile cilium1
intraciliary transport particle1
membrane-bounded organelle1
plasma membrane bounded cell projection1
cilium1
cellular anatomical structure1

Protein interactions and networks

STRING

790 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MORN5MORN3Q6PF18709
MORN5MORN4Q8NDC4642
MORN5CFAP95Q5VTT2639
MORN5CCER1Q8TC90594
MORN5CIMIP4O43247591
MORN5RIBC1Q8N443530
MORN5PEBP4Q96S96525
MORN5GARIN3Q8TC56519
MORN5GARIN5AQ6IPT2519
MORN5MORN1Q5T089514
MORN5GARIN4Q8IYT1509
MORN5NDUFA8P51970482
MORN5CFAP161Q6P656477
MORN5SCNM1Q9BWG6477
MORN5VSIG10LQ86VR7464

IntAct

32 interactions, top by confidence:

ABTypeScore
AGXTMORN5psi-mi:“MI:0915”(physical association)0.560
HAT1MORN5psi-mi:“MI:0915”(physical association)0.560
MORN5STAMBPL1psi-mi:“MI:0915”(physical association)0.560
MORN5MISPpsi-mi:“MI:0915”(physical association)0.560
MORN5POM121psi-mi:“MI:0915”(physical association)0.560
TLX3MORN5psi-mi:“MI:0915”(physical association)0.560
MORN5ENKD1psi-mi:“MI:0915”(physical association)0.560
MORN5GAS2L2psi-mi:“MI:0915”(physical association)0.560
USP2MORN5psi-mi:“MI:0915”(physical association)0.560
MORN5BCAT1psi-mi:“MI:0914”(association)0.530
AGXTMORN5psi-mi:“MI:0915”(physical association)0.000
HAT1MORN5psi-mi:“MI:0915”(physical association)0.000
STAMBPL1MORN5psi-mi:“MI:0915”(physical association)0.000
MISPMORN5psi-mi:“MI:0915”(physical association)0.000
POM121MORN5psi-mi:“MI:0915”(physical association)0.000
USP2MORN5psi-mi:“MI:0915”(physical association)0.000
TLX3MORN5psi-mi:“MI:0915”(physical association)0.000
ENKD1MORN5psi-mi:“MI:0915”(physical association)0.000
GAS2L2MORN5psi-mi:“MI:0915”(physical association)0.000

BioGRID (14): BCAT1 (Affinity Capture-MS), CHST15 (Affinity Capture-MS), DHTKD1 (Affinity Capture-MS), MORN5 (Two-hybrid), MORN5 (Two-hybrid), MORN5 (Two-hybrid), MORN5 (Two-hybrid), MORN5 (Two-hybrid), MORN5 (Two-hybrid), MORN5 (Two-hybrid), POM121 (Two-hybrid), GAS2L2 (Two-hybrid), CHST15 (Affinity Capture-MS), BCAT1 (Affinity Capture-MS)

ESM2 similar proteins: A0A3Q1N1R0, A0JMQ0, A2VE39, A2VEI2, A4IHS2, A7YT82, B3MHX6, B3NLK7, B4GIU9, B4HN85, B4J9K1, B4KQU8, B4LKS9, B4MYI5, B4P528, D2HRF1, E9Q5M6, O42131, O46374, O60551, O70311, P11388, Q02880, Q28FE4, Q28XF0, Q32LL6, Q32TF8, Q32TG3, Q4VBJ9, Q5JST6, Q5R981, Q5RAF3, Q5U2Z5, Q5VZ52, Q60HE5, Q64511, Q6GQ76, Q7K0Y1, Q7SXS8, Q7T0W1

Diamond homologs: Q28FE4, Q32LL6, Q4VBJ9, Q5VZ52, Q9DAI9

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance27
Likely benign0
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

747 predictions. Top by Δscore:

VariantEffectΔscore
9:122159986:G:GTdonor_gain1.0000
9:122166766:AG:Aacceptor_gain1.0000
9:122166767:GG:Gacceptor_gain1.0000
9:122174490:TTCAA:Tacceptor_loss1.0000
9:122174491:TCAAG:Tacceptor_loss1.0000
9:122174492:CAAG:Cacceptor_loss1.0000
9:122174493:AAG:Aacceptor_gain1.0000
9:122174493:AAGGT:Aacceptor_loss1.0000
9:122174495:G:GAacceptor_loss1.0000
9:122174629:T:Adonor_loss1.0000
9:122160001:GGGAA:Gdonor_gain0.9900
9:122160002:GGAA:Gdonor_gain0.9900
9:122160015:GGGAG:Gdonor_gain0.9900
9:122160016:GGAGG:Gdonor_gain0.9900
9:122160017:G:Tdonor_gain0.9900
9:122160017:GAGGT:Gdonor_loss0.9900
9:122160018:AGG:Adonor_loss0.9900
9:122160020:G:GCdonor_loss0.9900
9:122160021:T:Gdonor_loss0.9900
9:122166762:TTACA:Tacceptor_loss0.9900
9:122166763:TACA:Tacceptor_loss0.9900
9:122166764:ACAGG:Aacceptor_loss0.9900
9:122166765:CA:Cacceptor_loss0.9900
9:122166766:A:AGacceptor_gain0.9900
9:122166766:AGGAT:Aacceptor_gain0.9900
9:122166767:G:GCacceptor_loss0.9900
9:122166767:G:GGacceptor_gain0.9900
9:122166767:GGAT:Gacceptor_gain0.9900
9:122166767:GGATG:Gacceptor_gain0.9900
9:122171491:T:Gacceptor_gain0.9900

AlphaMissense

1073 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
9:122166892:T:AW58R0.991
9:122166892:T:CW58R0.991
9:122169657:T:CF70L0.988
9:122169659:C:AF70L0.988
9:122169659:C:GF70L0.988
9:122174570:T:GY128D0.986
9:122174620:A:CR144S0.986
9:122174620:A:TR144S0.986
9:122166886:G:CA56P0.983
9:122174565:G:AG126D0.983
9:122174592:T:AV135D0.983
9:122169701:C:GC84W0.982
9:122166811:T:GY31D0.981
9:122166857:T:CL46P0.981
9:122169670:T:CL74P0.980
9:122169720:T:CF91L0.980
9:122169722:T:AF91L0.980
9:122169722:T:GF91L0.980
9:122166817:G:TG33W0.979
9:122166894:G:CW58C0.978
9:122166894:G:TW58C0.978
9:122166893:G:CW58S0.977
9:122169690:T:AW81R0.977
9:122169690:T:CW81R0.977
9:122169715:G:CR89P0.976
9:122174619:G:CR144T0.976
9:122199919:T:GC158W0.976
9:122166818:G:AG33E0.975
9:122169700:G:AC84Y0.974
9:122166850:G:AG44R0.971

dbSNP variants (sampled 300 via entrez): RS1000009326 (9:122163490 A>G), RS1000038008 (9:122169919 G>C), RS1000278827 (9:122159820 A>C,G,T), RS1000479076 (9:122168252 C>G), RS1000638754 (9:122172667 C>T), RS1000768900 (9:122180411 G>A), RS1000882575 (9:122184595 G>T), RS1000987076 (9:122191846 T>G), RS1001018020 (9:122192005 T>A), RS1001023394 (9:122174316 G>C), RS1001070746 (9:122190720 A>G), RS1001176118 (9:122163194 A>G), RS1001207124 (9:122162876 G>A,T), RS1001217877 (9:122177322 C>G), RS1001248858 (9:122177080 C>A,T)

Disease associations

OMIM: gene MIM:619837 | disease phenotypes:

GenCC curated gene-disease

DiseaseClassificationInheritance
isolated cleft palateNo Known Disease RelationshipUnknown

Mondo (1): isolated cleft palate (MONDO:0007336)

Orphanet (0):

HPO phenotypes

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

GWAS associations

3 associations (top):

StudyTraitp-value
GCST010725_17Malaria5.000000e-06
GCST010725_29Malaria1.000000e-06
GCST010725_96Malaria9.000000e-07

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

15 total (human), top 15 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Aciddecreases methylation, increases expression3
Air Pollutantsincreases expression, increases abundance2
propionaldehydeincreases expression1
ethyl-p-hydroxybenzoatedecreases expression1
butyraldehydeincreases expression1
pentanalincreases expression1
entinostatincreases expression1
Vorinostatincreases expression1
Aldehydesincreases expression1
Amiodaroneincreases expression1
Fenfluramineincreases expression1
Silicon Dioxidedecreases expression1
Smokeincreases abundance, increases expression1
Tobacco Smoke Pollutiondecreases expression1
Cadmium Chloridedecreases expression1

Clinical trials (associated diseases)

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

  • Associated diseases: isolated cleft palate
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): isolated cleft palate