MROH9

gene
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Also known as FLJ23550ARMC11

Summary

MROH9 (maestro heat like repeat family member 9, HGNC:26287) is a protein-coding gene on chromosome 1q24.3, encoding Maestro heat-like repeat-containing protein family member 9 (Q5TGP6).

At a glance

  • GWAS associations: 23
  • Clinical variants (ClinVar): 90 total
  • MANE Select transcript: NM_001163629

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26287
Approved symbolMROH9
Namemaestro heat like repeat family member 9
Location1q24.3
Locus typegene with protein product
StatusApproved
AliasesFLJ23550, ARMC11
Ensembl geneENSG00000117501
Ensembl biotypeprotein_coding
Entrez80133

Gene structure

Transcript identifiers

Ensembl transcripts: 4 — 4 protein_coding

ENST00000367758, ENST00000367759, ENST00000426136, ENST00000864982

RefSeq mRNA: 2 — MANE Select: NM_001163629 NM_001163629, NM_025063

CCDS: CCDS41436, CCDS53429

Canonical transcript exons

ENST00000367759 — 22 exons

ExonStartEnd
ENSE00000814534170996507170996644
ENSE00001334212170995389170995531
ENSE00001445565171014117171014254
ENSE00001445566170998154170998274
ENSE00001628945170945520170945581
ENSE00001794090170947527170947573
ENSE00002209730171024649171024765
ENSE00002216322170983422170983534
ENSE00002218330171024395171024547
ENSE00002232985171062132171062194
ENSE00002234756170965151170965255
ENSE00002247407170971748170971883
ENSE00002247438170986561170986710
ENSE00002255155171025318171025420
ENSE00002270042170989855170990003
ENSE00002276155170935534170935587
ENSE00002276931170961890170961976
ENSE00002283655171016163171016336
ENSE00002284058171064099171064765
ENSE00002290450170992164170992329
ENSE00002305622170959462170959597
ENSE00002316232170958461170958540

Expression profiles

Bgee: expression breadth broad, 48 present calls, max score 79.70.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0045 / max 6.5644, expressed in 1 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
65860.00451

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047379.70silver quality
olfactory segment of nasal mucosaUBERON:000538673.39gold quality
right uterine tubeUBERON:000130269.74gold quality
bronchial epithelial cellCL:000232868.08gold quality
epithelium of bronchusUBERON:000203165.30gold quality
bronchusUBERON:000218564.41gold quality
mucosa of paranasal sinusUBERON:000503057.56gold quality
right lungUBERON:000216756.60gold quality
nasal cavity mucosaUBERON:000182656.03gold quality
lower lobe of lungUBERON:000894955.39silver quality
bone marrow cellCL:000209254.50gold quality
fallopian tubeUBERON:000388953.75gold quality
pancreatic ductal cellCL:000207952.17silver quality
left testisUBERON:000453351.24gold quality
testisUBERON:000047350.84gold quality
cranial nerve IIUBERON:000094150.14silver quality
right testisUBERON:000453450.12gold quality
epithelial cell of pancreasCL:000008349.84gold quality
Brodmann (1909) area 46UBERON:000648349.30gold quality
blood vessel layerUBERON:000479749.29gold quality
cervix squamous epitheliumUBERON:000692249.20gold quality
hair follicleUBERON:000207349.18gold quality
endometriumUBERON:000129549.12gold quality
olfactory bulbUBERON:000226448.92gold quality
choroid plexus epitheliumUBERON:000391148.89gold quality
myocardiumUBERON:000234948.87gold quality
type B pancreatic cellCL:000016948.83gold quality
quadriceps femorisUBERON:000137748.81gold quality
cardiac muscle of right atriumUBERON:000337948.55gold quality
CA1 field of hippocampusUBERON:000388148.50gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes5.16

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

27 targeting MROH9, 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-30A-5P100.0076.313233
HSA-MIR-30B-5P100.0076.293248
HSA-MIR-30C-5P100.0076.293248
HSA-MIR-30D-5P100.0076.323233
HSA-MIR-30E-5P100.0076.323242
HSA-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-98-3P100.0074.083907
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
HSA-MIR-7152-3P99.9767.47849
HSA-LET-7C-3P99.9573.422862
HSA-MIR-1236-3P99.9468.041695
HSA-MIR-4731-5P99.8967.232537
HSA-MIR-629-3P99.8567.991875
HSA-MIR-10393-3P99.7266.56961
HSA-MIR-6801-5P99.7266.50981
HSA-MIR-302B-5P99.5069.491857
HSA-MIR-302D-5P99.5069.341863
HSA-MIR-183-5P99.3172.271164
HSA-MIR-397399.2069.191990
HSA-MIR-1228-3P99.0066.53857
HSA-MIR-942-3P98.8169.04876
HSA-MIR-6867-3P98.1266.071305
HSA-MIR-446997.9365.811319
HSA-MIR-4667-5P97.6166.671683

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusMroh9ENSMUSG00000071890
rattus_norvegicusMroh9ENSRNOG00000003698

Paralogs (8): MROH8 (ENSG00000101353), MRO (ENSG00000134042), MROH2B (ENSG00000171495), MROH1 (ENSG00000179832), MROH7 (ENSG00000184313), MROH2A (ENSG00000185038), MROH6 (ENSG00000204839), MROH5 (ENSG00000226807)

Protein

Protein identifiers

Maestro heat-like repeat-containing protein family member 9Q5TGP6 (reviewed: Q5TGP6)

All UniProt accessions (2): H0Y687, Q5TGP6

Isoforms (2)

UniProt IDNamesCanonical?
Q5TGP6-11yes
Q5TGP6-22

RefSeq proteins (2): NP_001157101, NP_079339 (=MANE)

Domains & families (InterPro)

IDNameType
IPR016024ARM-type_foldHomologous_superfamily
IPR045206Maestro_heat-like_protFamily
IPR048465Maestro-like_HEATDomain

Pfam: PF21047

UniProt features (11 total): repeat 5, sequence variant 3, chain 1, sequence conflict 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q5TGP6-F176.950.34

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 37 (showing top): DODD_NASOPHARYNGEAL_CARCINOMA_DN, HMGA1_TARGET_GENES, MIR30B_5P_MIR30C_5P, MIR30D_5P, MIR30E_5P, MIR30A_5P, MIR4778_3P, MIR3123, MIR6797_5P, MIR1249_5P, MIR873_5P, MIR5585_3P, MIR4460, MIR140_5P, GSE13229_IMM_VS_MATURE_NKCELL_UP

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

326 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MROH9MROH2AA6NES4600
MROH9FAM217AQ8IXS0512
MROH9OR6M1Q8NGM8507
MROH9OR8H3Q8N146479
MROH9RSPH10B2B2RC85447
MROH9OR9G1Q8NH87444
MROH9MROH2BQ7Z745415
MROH9RSPH10BP0C881404
MROH9POPDC3Q9HBV1403
MROH9ANKRD29Q8N6D5401
MROH9CCDC81Q6ZN84398
MROH9MFSD6LQ8IWD5396
MROH9MIPOL1Q8TD10391
MROH9ARMC12Q5T9G4377
MROH9TMPRSS12Q86WS5377

IntAct

2 interactions, top by confidence:

ABTypeScore
GLO1MROH9psi-mi:“MI:0915”(physical association)0.400

BioGRID (3): MROH9 (Affinity Capture-MS), MROH9 (Affinity Capture-MS), MROH9 (Affinity Capture-MS)

ESM2 similar proteins: A0A0M3U1B0, A1A5Q6, A2AFS9, A2AVR2, A2CI98, A2CJ06, A2RTY3, A2RUW0, O70167, O70173, P0C2Y1, P15304, P59729, Q08EC4, Q3SYK4, Q3TYG6, Q3U1D0, Q4R744, Q4R9E9, Q5R4B2, Q5T4T6, Q5TGP6, Q5VWK0, Q68CQ1, Q6AYJ3, Q6IFT4, Q6IRU7, Q6REY9, Q6ZUA9, Q7Z572, Q80VH0, Q86WZ0, Q86XG9, Q8C0X8, Q8CCC3, Q8ND61, Q8NDZ2, Q8TB24, Q96M43, Q96QP1

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance71
Likely benign13
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

2435 predictions. Top by Δscore:

VariantEffectΔscore
1:170958447:A:AGacceptor_gain1.0000
1:170958447:AACAT:Aacceptor_gain1.0000
1:170958448:A:Gacceptor_gain1.0000
1:170958448:ACAT:Aacceptor_gain1.0000
1:170958450:AT:Aacceptor_gain1.0000
1:170958451:T:Gacceptor_gain1.0000
1:170958451:T:TAacceptor_gain1.0000
1:170959460:A:AGacceptor_gain1.0000
1:170959460:AG:Aacceptor_loss1.0000
1:170959461:G:GGacceptor_gain1.0000
1:170959461:GC:Gacceptor_gain1.0000
1:170959461:GCTTT:Gacceptor_gain1.0000
1:170959595:G:GTdonor_gain1.0000
1:170961985:GAAA:Gdonor_gain1.0000
1:170961988:A:Gdonor_gain1.0000
1:170971747:GATAA:Gacceptor_gain1.0000
1:170989999:GACGA:Gdonor_gain1.0000
1:170990002:GA:Gdonor_gain1.0000
1:170990004:G:GGdonor_gain1.0000
1:170992282:G:GTdonor_gain1.0000
1:170992287:G:Tdonor_gain1.0000
1:170992341:GA:Gdonor_gain1.0000
1:170995498:G:GGdonor_gain1.0000
1:170995527:GCTTT:Gdonor_gain1.0000
1:170995532:G:GGdonor_gain1.0000
1:170996640:GC:Gdonor_gain1.0000
1:170996640:GCTAA:Gdonor_gain1.0000
1:170996641:C:CGdonor_gain1.0000
1:170996641:C:Gdonor_gain1.0000
1:170996645:G:GGdonor_gain1.0000

AlphaMissense

5716 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
1:170992180:T:AW349R0.988
1:170992180:T:CW349R0.988
1:170995462:T:CL423P0.978
1:170995452:T:CF420L0.969
1:170995454:C:AF420L0.969
1:170995454:C:GF420L0.969
1:170998173:T:CF499L0.969
1:170998175:T:AF499L0.969
1:170998175:T:GF499L0.969
1:170992182:G:CW349C0.967
1:170992182:G:TW349C0.967
1:170996641:C:AA491D0.967
1:170992244:T:CL370P0.965
1:170996551:T:CL461P0.963
1:170989969:T:CF332L0.962
1:170989971:T:AF332L0.962
1:170989971:T:GF332L0.962
1:170971791:T:CL175P0.960
1:170989976:T:CL334P0.960
1:170995474:T:CL427P0.959
1:170996533:T:CL455P0.955
1:170971772:G:CG169R0.953
1:170986600:T:CF257L0.953
1:170986602:T:AF257L0.953
1:170986602:T:GF257L0.953
1:170995390:C:AA399E0.953
1:170995453:T:CF420S0.953
1:170995465:T:CL424S0.953
1:170996536:T:CL456P0.951
1:170971784:G:CA173P0.950

dbSNP variants (sampled 300 via entrez): RS1000044245 (1:171054289 C>T), RS1000053600 (1:171005916 T>C), RS1000105914 (1:171017009 T>G), RS1000121490 (1:171002202 C>T), RS1000194456 (1:171063991 T>C,G), RS1000226289 (1:170989084 A>G), RS1000236354 (1:171008609 A>C), RS1000241693 (1:171041469 C>T), RS1000251141 (1:170967758 T>C), RS1000338236 (1:170996436 G>T), RS1000362462 (1:171014294 T>A,C), RS1000369166 (1:171054724 T>C), RS1000379877 (1:171060454 A>G), RS1000415430 (1:171042302 T>C), RS1000448246 (1:171019567 C>G,T)

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

23 associations (top):

StudyTraitp-value
GCST005580_163Intraocular pressure1.000000e-08
GCST005580_267Intraocular pressure4.000000e-10
GCST010002_370Refractive error3.000000e-11
GCST011011_3Youthful appearance (self-reported)3.000000e-08
GCST012020_36Serum metabolite levels2.000000e-15
GCST012094_6Major depressive disorder and major depressive episode treated with electroconvulsive therapy4.000000e-06
GCST012095_6Major depressive episode treated with electroconvulsive therapy5.000000e-07
GCST012226_589Waist circumference adjusted for body mass index1.000000e-09
GCST012226_590Waist circumference adjusted for body mass index6.000000e-11
GCST012231_159A body shape index2.000000e-08
GCST90011866_7Systemic lupus erythematosus7.000000e-08
GCST90020026_644Hip index2.000000e-13
GCST90020026_648Hip index2.000000e-12
GCST90020026_650Hip index5.000000e-09
GCST90020026_651Hip index1.000000e-08
GCST90020028_225Hip circumference adjusted for BMI7.000000e-10
GCST90020028_252Hip circumference adjusted for BMI4.000000e-13
GCST90020028_253Hip circumference adjusted for BMI8.000000e-14
GCST90020028_254Hip circumference adjusted for BMI2.000000e-08
GCST90020028_255Hip circumference adjusted for BMI1.000000e-09
GCST90020028_256Hip circumference adjusted for BMI8.000000e-10
GCST90020028_257Hip circumference adjusted for BMI5.000000e-09
GCST90020029_1098Waist circumference adjusted for body mass index3.000000e-08

EFO canonical traits (4, from GWAS)

EFO IDTrait name
EFO:0004695intraocular pressure measurement
EFO:0007634major depressive episode
EFO:0007789BMI-adjusted waist circumference
EFO:0008039BMI-adjusted hip circumference

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

8 total (human), top 8 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneaffects methylation, increases expression2
bisphenol Aaffects cotreatment, decreases methylation1
S-(1,2-dichlorovinyl)cysteineaffects cotreatment, increases expression1
Fulvestrantaffects cotreatment, decreases methylation1
Acetaminophendecreases expression1
Cadmiumdecreases expression1
Lipopolysaccharidesaffects cotreatment, increases expression1
Tobacco Smoke Pollutiondecreases 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.