BRD3OS

gene
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Also known as FLJ35348bA374P20.3SERLOC

Summary

BRD3OS (BRD3 opposite strand, HGNC:24742) is a protein-coding gene on chromosome 9q34.2, encoding Uncharacterized protein BRD3OS (A0A1B0GUI7).

At a glance

  • GWAS associations: 3
  • Clinical variants (ClinVar): 3 total
  • MANE Select transcript: NM_001355256

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:24742
Approved symbolBRD3OS
NameBRD3 opposite strand
Location9q34.2
Locus typegene with protein product
StatusApproved
AliasesFLJ35348, bA374P20.3, SERLOC
Ensembl geneENSG00000235106
Ensembl biotypeprotein_coding
Entrez266655

Gene structure

Transcript identifiers

Ensembl transcripts: 13 — 9 protein_coding, 4 protein_coding_CDS_not_defined

ENST00000432807, ENST00000550853, ENST00000552018, ENST00000603928, ENST00000605164, ENST00000624381, ENST00000906125, ENST00000906126, ENST00000906127, ENST00000922048, ENST00000922049, ENST00000922050, ENST00000922051

RefSeq mRNA: 1 — MANE Select: NM_001355256 NM_001355256

CCDS: CCDS87707

Canonical transcript exons

ENST00000603928 — 3 exons

ExonStartEnd
ENSE00001598635134025481134025536
ENSE00001614819134025845134026090
ENSE00003660396134026208134031587

Expression profiles

Bgee: expression breadth ubiquitous, 274 present calls, max score 93.83.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 18.3312 / max 109.5274, expressed in 1754 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
9929717.53901747
992960.5053300
2056550.286958

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bronchial epithelial cellCL:000232893.83gold quality
epithelium of bronchusUBERON:000203192.21gold quality
buccal mucosa cellCL:000233691.97silver quality
bronchusUBERON:000218591.63gold quality
middle temporal gyrusUBERON:000277190.94gold quality
right frontal lobeUBERON:000281090.45gold quality
prefrontal cortexUBERON:000045190.11gold quality
adenohypophysisUBERON:000219689.75gold quality
cortical plateUBERON:000534389.45gold quality
amygdalaUBERON:000187689.43gold quality
cingulate cortexUBERON:000302789.28gold quality
pituitary glandUBERON:000000789.24gold quality
anterior cingulate cortexUBERON:000983589.12gold quality
temporal lobeUBERON:000187188.98gold quality
corpus epididymisUBERON:000435988.91gold quality
entorhinal cortexUBERON:000272888.88gold quality
dorsolateral prefrontal cortexUBERON:000983488.87gold quality
nucleus accumbensUBERON:000188288.84gold quality
neocortexUBERON:000195088.83gold quality
frontal cortexUBERON:000187088.68gold quality
cerebral cortexUBERON:000095688.57gold quality
primary visual cortexUBERON:000243688.47gold quality
Ammon’s hornUBERON:000195488.40gold quality
caudate nucleusUBERON:000187388.30gold quality
right uterine tubeUBERON:000130288.24gold quality
telencephalonUBERON:000189388.22gold quality
Brodmann (1909) area 9UBERON:001354088.22gold quality
forebrainUBERON:000189088.21gold quality
secondary oocyteCL:000065587.82gold quality
ventricular zoneUBERON:000305387.79gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.10

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Results identified LINC00094 to be downregulated in the lung squamous cell carcinoma tissues of smoking patients and may play an important role in diagnosis and prognosis. (PMID:28949095)

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Uncharacterized protein BRD3OSA0A1B0GUI7 (reviewed: A0A1B0GUI7)

Alternative names: BRD3 opposite strand protein, Long intergenic non-protein coding RNA 94, Non-protein coding RNA 94

All UniProt accessions (1): A0A1B0GUI7

RefSeq proteins (1): NP_001342185* (*=MANE)

Domains & families (InterPro)

UniProt features (1 total): chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A1B0GUI7-F167.590.00

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 72 (showing top): LUCAS_HNF4A_TARGETS_DN, DOUGLAS_BMI1_TARGETS_UP, STEIN_ESRRA_TARGETS_DN, MOREAUX_MULTIPLE_MYELOMA_BY_TACI_UP, CHICAS_RB1_TARGETS_SENESCENT, FORTSCHEGGER_PHF8_TARGETS_DN, PHONG_TNF_RESPONSE_VIA_P38_COMPLETE, BLUM_RESPONSE_TO_SALIRASIB_DN, chr9q34, ARID5B_TARGET_GENES, CEBPZ_TARGET_GENES, KAT2A_TARGET_GENES, KLF14_TARGET_GENES, MEF2D_TARGET_GENES, SFMBT1_TARGET_GENES

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

68 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
BRD3OSTMEM50AO95807470
BRD3OSCEP68Q76N32434
BRD3OSLRP5LA4QPB2431
BRD3OSFERRY3Q9NQ89419
BRD3OSGOLT1BQ9Y3E0357
BRD3OSRWDD3Q9Y3V2348
BRD3OSSH3GL2Q99962316
BRD3OSPARP11Q9NR21300
BRD3OSALG1L2C9J202297
BRD3OSBRD3Q15059247
BRD3OSSAXO4Q7Z5V6234
BRD3OSCDONQ4KMG0221
BRD3OSDLC1Q96QB1220
BRD3OSAARDQ4LEZ3220
BRD3OSANTXR2P58335218

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A1B0GUI7, A1DL98, A1L1K4, A4V8B4, A6QLJ4, A6ZMG4, A6ZR60, A7NVJ4, A9JR56, B3LLZ8, C5E1C7, C7GWA2, C8ZEW0, O13916, O60153, P0C2W9, P15130, P16135, P20486, P27271, P28974, P35198, P40063, P84395, Q04438, Q28EW5, Q28GG3, Q4V853, Q5FVD7, Q5R4F8, Q5R977, Q5RD94, Q5U550, Q66657, Q68EK9, Q68FR5, Q6AX78, Q6C3T0, Q751I6, Q7T2A3

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

315 predictions. Top by Δscore:

VariantEffectΔscore
9:134032165:TCTG:Tacceptor_gain0.8800
9:134033701:CTTCT:Cacceptor_gain0.8800
9:134032166:C:Gacceptor_gain0.8400
9:134034053:C:CCacceptor_gain0.8000
9:134033706:C:CCacceptor_gain0.7900
9:134033704:CT:Cacceptor_gain0.7600
9:134033702:TTCT:Tacceptor_gain0.7200
9:134033453:C:CCacceptor_gain0.7100
9:134033703:TCT:Tacceptor_gain0.6700
9:134033704:CTC:Cacceptor_gain0.6700
9:134033705:TCT:Tacceptor_gain0.6700
9:134033919:A:Tdonor_gain0.6700
9:134033702:TTCTC:Tacceptor_loss0.6500
9:134033703:TCTCT:Tacceptor_loss0.6500
9:134033705:TC:Tacceptor_loss0.6500
9:134033706:C:CAacceptor_loss0.6500
9:134033707:T:Aacceptor_loss0.6500
9:134033715:CA:Cacceptor_loss0.6300
9:134033716:A:Tacceptor_loss0.6300
9:134033710:GGAGA:Gacceptor_loss0.6100
9:134033711:GAGA:Gacceptor_loss0.6100
9:134033449:AAAA:Aacceptor_gain0.6000
9:134033709:TGGA:Tacceptor_loss0.6000
9:134034050:TGA:Tacceptor_gain0.6000
9:134032164:CT:Cacceptor_gain0.5700
9:134034052:A:ACacceptor_gain0.5700
9:134033522:C:CTdonor_gain0.5600
9:134033780:A:Tacceptor_gain0.5600
9:134032164:C:Aacceptor_gain0.5500
9:134033922:A:Cdonor_gain0.5300

AlphaMissense

539 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
9:134026935:T:AV63D0.952
9:134026834:G:CW29C0.930
9:134026834:G:TW29C0.930
9:134026832:T:AW29R0.921
9:134026832:T:CW29R0.921
9:134026808:T:GY21D0.914
9:134026917:G:TG57V0.908
9:134026815:A:TD23V0.905
9:134026895:A:CS50R0.903
9:134026897:C:AS50R0.903
9:134026897:C:GS50R0.903
9:134026921:T:AN58K0.888
9:134026921:T:GN58K0.888
9:134026779:C:AA11D0.883
9:134026929:T:AI61N0.880
9:134026920:A:TN58I0.878
9:134026821:C:TS25F0.872
9:134026929:T:GI61S0.863
9:134026806:G:CR20P0.861
9:134026821:C:AS25Y0.859
9:134026815:A:CD23A0.844
9:134026820:T:CS25P0.842
9:134026842:A:CQ32P0.842
9:134026990:C:GC81W0.836
9:134026904:T:GY53D0.835
9:134026809:A:CY21S0.831
9:134026889:A:CS48R0.830
9:134026891:C:AS48R0.830
9:134026891:C:GS48R0.830
9:134026833:G:CW29S0.825

dbSNP variants (sampled 300 via entrez): RS1000163096 (9:134030144 G>A), RS1000258945 (9:134025556 TG>T), RS1000288628 (9:134025779 G>C), RS1001095836 (9:134025407 A>T), RS1001932257 (9:134026597 C>G,T), RS1001957939 (9:134031430 G>A), RS1001970082 (9:134026816 C>T), RS1002238570 (9:134031275 C>A,T), RS1002362162 (9:134025883 G>A), RS1002827296 (9:134027346 C>A), RS1002903400 (9:134026075 G>T), RS1003103851 (9:134027123 C>A), RS1003510175 (9:134032072 G>A,C), RS1003878326 (9:134024868 G>A,C), RS1003950297 (9:134024571 C>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

3 associations (top):

StudyTraitp-value
GCST90002386_440High light scatter reticulocyte percentage of red cells3.000000e-09
GCST90002400_694Plateletcrit4.000000e-10
GCST90002401_199Platelet distribution width1.000000e-15

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0007985platelet crit
EFO:0007984platelet component distribution width

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

25 total (human), top 25 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, increases expression3
Smokedecreases expression, increases abundance, increases expression2
aristolochic acid Idecreases expression1
triphenyl phosphateaffects expression1
bisphenol Aaffects methylation1
tris(1,3-dichloro-2-propyl)phosphatedecreases expression1
sodium arsenitedecreases expression1
ferrous chloridedecreases expression1
avobenzonedecreases expression1
di-n-butylphosphoric acidaffects expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamidedecreases expression, affects cotreatment1
dorsomorphindecreases expression, affects cotreatment1
Sunitinibincreases expression1
Air Pollutantsincreases abundance, increases expression1
Benzo(a)pyreneaffects methylation1
Phenylmercuric Acetateaffects cotreatment, decreases expression1
Silicon Dioxidedecreases expression1
Thiramdecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Tretinoinincreases expression1
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxidedecreases expression1
Gold Compoundsincreases expression1
Cadmium Chloridedecreases expression1
Acrylamidedecreases expression1
tert-Butylhydroperoxidedecreases 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.