MROH7

gene
On this page

Also known as FLJ46354

Summary

MROH7 (maestro heat like repeat family member 7, HGNC:24802) is a protein-coding gene on chromosome 1p32.3, encoding Maestro heat-like repeat-containing protein family member 7 (Q68CQ1).

Located in extracellular space.

Source: NCBI Gene 374977 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 228 total
  • MANE Select transcript: NM_001039464

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:24802
Approved symbolMROH7
Namemaestro heat like repeat family member 7
Location1p32.3
Locus typegene with protein product
StatusApproved
AliasesFLJ46354
Ensembl geneENSG00000184313
Ensembl biotypeprotein_coding
Entrez374977

Gene structure

Transcript identifiers

Ensembl transcripts: 14 — 5 protein_coding, 5 nonsense_mediated_decay, 2 retained_intron, 2 protein_coding_CDS_not_defined

ENST00000339553, ENST00000371287, ENST00000395690, ENST00000409996, ENST00000413188, ENST00000421030, ENST00000422659, ENST00000438846, ENST00000440047, ENST00000440217, ENST00000472987, ENST00000478097, ENST00000493533, ENST00000857672

RefSeq mRNA: 2 — MANE Select: NM_001039464 NM_001039464, NM_001291332

CCDS: CCDS41342

Canonical transcript exons

ENST00000421030 — 24 exons

ExonStartEnd
ENSE000018934745470994654710266
ENSE000019582195464178654641968
ENSE000034746335467874254678854
ENSE000034895615467401654674151
ENSE000035327865470032154700461
ENSE000035542395467989154680045
ENSE000035670125469242454692561
ENSE000035808665467926354679439
ENSE000035954545469537654695490
ENSE000036617145468265654682794
ENSE000036853975468625854686448
ENSE000036950305466516754665240
ENSE000036978965465285354654157
ENSE000036981945466885454668937
ENSE000036985555470901454709076
ENSE000036986755467049754670576
ENSE000036987495470262354702745
ENSE000036987915470643554706537
ENSE000036993615467370154673805
ENSE000036995155467309154673186
ENSE000036997705470209054702245
ENSE000037005255470114354701322
ENSE000037014205465194954651983
ENSE000037015795467080054670929

Expression profiles

Bgee: expression breadth ubiquitous, 137 present calls, max score 96.09.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0157 / max 9.0217, expressed in 5 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
29580.09053
29600.01215
29570.00724
29590.00363

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right testisUBERON:000453496.09gold quality
left testisUBERON:000453395.99gold quality
testisUBERON:000047394.77gold quality
pituitary glandUBERON:000000788.96gold quality
adenohypophysisUBERON:000219687.70gold quality
apex of heartUBERON:000209887.45gold quality
left lobe of thyroid glandUBERON:000112086.44gold quality
thyroid glandUBERON:000204686.38gold quality
right lobe of thyroid glandUBERON:000111985.13gold quality
lower esophagus muscularis layerUBERON:003583381.95gold quality
lower esophagusUBERON:001347381.89gold quality
heart left ventricleUBERON:000208481.60gold quality
right uterine tubeUBERON:000130281.18gold quality
esophagogastric junction muscularis propriaUBERON:003584181.06gold quality
muscle layer of sigmoid colonUBERON:003580580.70gold quality
sigmoid colonUBERON:000115980.66gold quality
right atrium auricular regionUBERON:000663180.39gold quality
hindlimb stylopod muscleUBERON:000425280.07gold quality
heartUBERON:000094879.76gold quality
left ovaryUBERON:000211979.59gold quality
mucosa of transverse colonUBERON:000499179.56gold quality
right ovaryUBERON:000211879.36gold quality
fundus of stomachUBERON:000116079.26gold quality
transverse colonUBERON:000115778.99gold quality
ovaryUBERON:000099278.56gold quality
colonUBERON:000115578.47gold quality
caudate nucleusUBERON:000187378.14gold quality
ascending aortaUBERON:000149677.70gold quality
prostate glandUBERON:000236777.56gold quality
thoracic aortaUBERON:000151577.51gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.67

Regulation

Is transcription factor: no

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusMroh7ENSMUSG00000047502
rattus_norvegicusMroh7ENSRNOG00000058870

Paralogs (8): MROH8 (ENSG00000101353), MROH9 (ENSG00000117501), MRO (ENSG00000134042), MROH2B (ENSG00000171495), MROH1 (ENSG00000179832), MROH2A (ENSG00000185038), MROH6 (ENSG00000204839), MROH5 (ENSG00000226807)

Protein

Protein identifiers

Maestro heat-like repeat-containing protein family member 7Q68CQ1 (reviewed: Q68CQ1)

Alternative names: HEAT repeat-containing protein 8

All UniProt accessions (5): B7ZBM2, F8W8P2, F8WE25, F8WFA2, Q68CQ1

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Miscellaneous. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay.

Isoforms (6)

UniProt IDNamesCanonical?
Q68CQ1-71yes
Q68CQ1-22
Q68CQ1-83
Q68CQ1-44
Q68CQ1-95
Q68CQ1-16

RefSeq proteins (2): NP_001034553, NP_001278261 (=MANE)

Domains & families (InterPro)

IDNameType
IPR011989ARM-likeHomologous_superfamily
IPR016024ARM-type_foldHomologous_superfamily
IPR045206Maestro_heat-like_protFamily
IPR048465Maestro-like_HEATDomain
IPR055406HEAT_MaestroDomain
IPR055408HEAT_MROH2B-likeDomain

Pfam: PF21047, PF23210, PF23227

UniProt features (37 total): splice variant 10, sequence variant 10, repeat 4, glycosylation site 3, sequence conflict 3, region of interest 3, transmembrane region 2, chain 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q68CQ1-F166.690.33

Functional residue map

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

Glycosylation sites (3): 318, 438, 586

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 40 (showing top): GGTGTGT_MIR329, TGACCTY_ERR1_Q2, GNF2_CCNA1, ATCATGA_MIR433, GGTGAAG_MIR412, MULLIGHAN_MLL_SIGNATURE_2_DN, LEIN_CHOROID_PLEXUS_MARKERS, ER_Q6_02, MULLIGHAN_MLL_SIGNATURE_1_DN, ER_Q6_01, ZWANG_EGF_INTERVAL_UP, JAK2_DN.V1_DN, NFKBIA_TARGET_GENES, SRPK2_TARGET_GENES, ZNF22_TARGET_GENES

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (3): obsolete extracellular space (GO:0005615), cytoplasm (GO:0005737), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure2
intracellular anatomical structure1

Protein interactions and networks

STRING

330 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MROH7CDCP2Q5VXM1541
MROH7WDR27A2RRH5457
MROH7SMIM21Q3B7S5447
MROH7LDLRAD1Q5T700434
MROH7HEATR4Q86WZ0433
MROH7MROH2BQ7Z745429
MROH7TMEM178BH3BS89416
MROH7ARRDC2Q8TBH0414
MROH7TTC4O95801408
MROH7RSPH14Q9UHP6405
MROH7TANGO6Q9C0B7397
MROH7REXO2Q9Y3B8396
MROH7A8MUN0A8MUN0394
MROH7SLC35F6Q8N357379
MROH7CAPN7Q9Y6W3375

IntAct

0 interactions, top by confidence:

BioGRID (5): MROH7 (Affinity Capture-MS), MROH7 (Affinity Capture-MS), MROH7 (Affinity Capture-MS), MROH7 (Cross-Linking-MS (XL-MS)), MROH7 (Protein-peptide)

ESM2 similar proteins: A1A5P9, A2AVR2, A6QPT6, B2KFW1, O14978, P17029, P17040, P17098, P25233, P70503, Q13342, Q14D33, Q3SYK4, Q3V3Q4, Q4KLI1, Q4R8H9, Q4V8E9, Q5PPP4, Q5R670, Q5R7U0, Q5VWK0, Q61066, Q63HK3, Q68CQ1, Q6PCZ4, Q7TS72, Q80ZG2, Q8BGS3, Q8CF60, Q8IWY8, Q8N660, Q8NDZ0, Q8TD17, Q921B4, Q923B3, Q96D09, Q96GC6, Q96JL9, Q96M43, Q99608

Diamond homologs: A2AVR2, A2RUW0, Q68CQ1, A6NGR9, A7E2Y6

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance206
Likely benign21
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

5606 predictions. Top by Δscore:

VariantEffectΔscore
1:54670572:C:Gdonor_gain1.0000
1:54670786:T:Aacceptor_gain1.0000
1:54670786:T:TAacceptor_gain1.0000
1:54670798:A:AGacceptor_gain1.0000
1:54670799:G:GAacceptor_gain1.0000
1:54670799:G:GGacceptor_gain1.0000
1:54670799:GC:Gacceptor_gain1.0000
1:54670799:GCC:Gacceptor_gain1.0000
1:54670799:GCCA:Gacceptor_gain1.0000
1:54670799:GCCAC:Gacceptor_gain1.0000
1:54670926:CCAG:Cdonor_loss1.0000
1:54670926:CCAGG:Cdonor_loss1.0000
1:54670927:CAGGT:Cdonor_loss1.0000
1:54670930:GTGAG:Gdonor_loss1.0000
1:54670931:T:Adonor_loss1.0000
1:54678738:GCAGG:Gacceptor_loss1.0000
1:54678739:CA:Cacceptor_loss1.0000
1:54678740:A:AGacceptor_gain1.0000
1:54678741:G:GGacceptor_gain1.0000
1:54678741:G:GTacceptor_loss1.0000
1:54678741:GGA:Gacceptor_gain1.0000
1:54679257:TTTCA:Tacceptor_loss1.0000
1:54679259:TCA:Tacceptor_loss1.0000
1:54679260:CA:Cacceptor_loss1.0000
1:54679260:CAG:Cacceptor_loss1.0000
1:54679261:AG:Aacceptor_gain1.0000
1:54679262:G:Aacceptor_loss1.0000
1:54679262:GG:Gacceptor_gain1.0000
1:54679262:GGA:Gacceptor_gain1.0000
1:54679405:TGCTG:Tdonor_gain1.0000

AlphaMissense

8651 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
1:54682672:T:AW800R0.998
1:54682672:T:CW800R0.998
1:54692506:T:AW932R0.996
1:54692506:T:CW932R0.996
1:54700322:T:CL989P0.996
1:54682674:G:CW800C0.995
1:54682674:G:TW800C0.995
1:54692508:G:CW932C0.995
1:54692508:G:TW932C0.995
1:54695426:T:CL967P0.995
1:54686331:T:CL865P0.994
1:54692542:G:AG944R0.994
1:54692542:G:CG944R0.994
1:54695377:G:CA951P0.994
1:54695477:C:AA984D0.994
1:54692543:G:AG944E0.993
1:54692558:C:AA949E0.993
1:54695468:C:AT981K0.993
1:54695471:C:AA982D0.993
1:54700430:G:AG1025D0.993
1:54682673:G:CW800S0.992
1:54686334:T:CL866P0.992
1:54692450:T:CL913P0.992
1:54695470:G:CA982P0.992
1:54700360:T:CY1002H0.992
1:54700429:G:CG1025R0.992
1:54686321:T:GY862D0.991
1:54700349:T:CI998T0.991
1:54686262:C:AA842D0.990
1:54686268:G:AG844D0.990

dbSNP variants (sampled 300 via entrez): RS1000000936 (1:54657579 G>A), RS1000011373 (1:54708862 C>G,T), RS1000074963 (1:54654612 A>G), RS1000110360 (1:54703185 C>A), RS1000240504 (1:54679737 C>T), RS1000263189 (1:54710571 G>A), RS1000312737 (1:54645530 C>G), RS1000321661 (1:54689830 C>T), RS1000350964 (1:54685495 C>T), RS1000366590 (1:54645279 T>G), RS1000423852 (1:54691891 C>T), RS1000566167 (1:54700983 G>A), RS1000584967 (1:54662167 C>A), RS1000615167 (1:54707427 T>C), RS1000621425 (1:54643636 CAG>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

2 associations (top):

StudyTraitp-value
GCST003833_20Adult asthma9.000000e-07
GCST003833_9Adult asthma2.000000e-06

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

17 total (human), top 17 by PubMed support.

ChemicalActions (top 5)PubMed papers
terbufosincreases methylation1
benzo(e)pyreneincreases methylation1
(+)-JQ1 compoundincreases expression1
Resveratrolaffects cotreatment, decreases expression1
Sunitinibincreases expression1
Benzo(a)pyreneaffects methylation1
Fonofosincreases methylation1
Formaldehydedecreases expression1
Methapyrileneincreases methylation1
Oxygenincreases expression1
Parathionincreases methylation1
Plant Extractsaffects cotreatment, decreases expression1
Silicon Dioxidedecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Triclosandecreases expression1
Aflatoxin B1decreases methylation1
S-Nitrosoglutathionedecreases 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.