TMEM265

gene
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Summary

TMEM265 (transmembrane protein 265, HGNC:51241) is a protein-coding gene on chromosome 16p11.2, encoding Transmembrane protein 265 (A0A087WTH1).

Predicted to be located in membrane.

Source: NCBI Gene 100862671 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 2 total
  • MANE Select transcript: NM_001256829

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:51241
Approved symbolTMEM265
Nametransmembrane protein 265
Location16p11.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000281991
Ensembl biotypeprotein_coding
Entrez100862671

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000615541

RefSeq mRNA: 1 — MANE Select: NM_001256829 NM_001256829

CCDS: CCDS73870

Canonical transcript exons

ENST00000615541 — 3 exons

ExonStartEnd
ENSE000037416583074378230745196
ENSE000037437893074174130741908
ENSE000037514533074064230740707

Expression profiles

Bgee: expression breadth ubiquitous, 112 present calls, max score 85.68.

FANTOM5 (CAGE): breadth broad, TPM avg 3.4122 / max 121.2574, expressed in 569 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1537183.0485547
1537170.2048125
1537160.158998

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
lower esophagus mucosaUBERON:003583485.68gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099182.57gold quality
skin of abdomenUBERON:000141679.76gold quality
esophagus mucosaUBERON:000246979.53gold quality
olfactory segment of nasal mucosaUBERON:000538678.61gold quality
zone of skinUBERON:000001478.34gold quality
skin of legUBERON:000151177.80gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047377.58gold quality
right lungUBERON:000216775.88gold quality
minor salivary glandUBERON:000183067.75gold quality
upper lobe of left lungUBERON:000895267.38gold quality
mucosa of transverse colonUBERON:000499166.64gold quality
metanephros cortexUBERON:001053366.35gold quality
saliva-secreting glandUBERON:000104465.35gold quality
lungUBERON:000204862.70gold quality
left lobe of thyroid glandUBERON:000112061.47gold quality
thyroid glandUBERON:000204660.27gold quality
vaginaUBERON:000099658.92gold quality
esophagusUBERON:000104356.65gold quality
cerebellar hemisphereUBERON:000224556.26gold quality
gall bladderUBERON:000211056.18gold quality
cerebellumUBERON:000203755.25gold quality
cerebellar cortexUBERON:000212955.13gold quality
right hemisphere of cerebellumUBERON:001489053.38gold quality
right lobe of thyroid glandUBERON:000111953.32gold quality
transverse colonUBERON:000115749.61gold quality
adenohypophysisUBERON:000219648.71gold quality
adult mammalian kidneyUBERON:000008247.25gold quality
right uterine tubeUBERON:000130247.06gold quality
islet of LangerhansUBERON:000000646.82gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

78 targeting TMEM265, 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-3134100.0066.43777
HSA-MIR-340-5P100.0072.504437
HSA-MIR-318599.9968.121959
HSA-MIR-477599.9875.006394
HSA-MIR-590-3P99.9674.346478
HSA-MIR-365899.9673.874379
HSA-MIR-129799.9173.413162
HSA-MIR-106A-5P99.9073.942683
HSA-MIR-17-5P99.8973.832665
HSA-MIR-106B-5P99.8874.722795
HSA-MIR-20A-5P99.8874.762769
HSA-MIR-6780A-5P99.8866.692776
HSA-MIR-20B-5P99.8874.012621
HSA-MIR-519D-3P99.8873.972607
HSA-MIR-526B-3P99.8874.062587
HSA-MIR-93-5P99.8873.982606
HSA-MIR-10395-5P99.8667.35676
HSA-MIR-76599.8468.242442
HSA-MIR-6875-3P99.8270.262983
HSA-MIR-26A-5P99.7873.522303
HSA-MIR-26B-5P99.7873.512305
HSA-MIR-57799.7869.132479
HSA-MIR-1273H-5P99.7766.322471
HSA-MIR-11181-3P99.7566.382205
HSA-MIR-556-3P99.7468.751203
HSA-MIR-446599.7172.562096
HSA-MIR-30B-3P99.7065.762325
HSA-MIR-3689A-3P99.7065.732306
HSA-MIR-3689B-3P99.7065.712311
HSA-MIR-3689C99.7065.712311

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Transmembrane protein 265A0A087WTH1 (reviewed: A0A087WTH1)

All UniProt accessions (1): A0A087WTH1

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the CD225/Dispanin family.

RefSeq proteins (1): NP_001243758* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR007593CD225/Dispanin_famFamily

Pfam: PF04505

UniProt features (3 total): transmembrane region 2, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A087WTH1-F171.120.06

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 57 (showing top): ENK_UV_RESPONSE_KERATINOCYTE_UP, BROWNE_HCMV_INFECTION_12HR_UP, BROWNE_HCMV_INFECTION_24HR_UP, BLALOCK_ALZHEIMERS_DISEASE_UP, chr16p11, FOURNIER_ACINAR_DEVELOPMENT_EARLY_UP, ZHANG_RESPONSE_TO_IKK_INHIBITOR_AND_TNF_UP, PHONG_TNF_RESPONSE_NOT_VIA_P38, PBXIP1_TARGET_GENES, MIR1297, MIR106B_5P, MIR20A_5P, MIR106A_5P, MIR17_5P, MIR20B_5P

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (1): membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure1

Protein interactions and networks

STRING

64 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM265GLB1LQ6UWU2696
TMEM265A0A087WTJ2A0A087WTJ2621
TMEM265MLF1P58340506
TMEM265CES4AQ5XG92477
TMEM265SIRPB1O00241390
TMEM265NUP160Q12769360
TMEM265TCN2P20062349
TMEM265U2AF1Q01081348
TMEM265MTHFD1LQ6UB35348
TMEM265MYL11Q96A32336
TMEM265DTLQ9NZJ0314
TMEM265PSMA2P25787160
TMEM265CASP6P552120
TMEM265MALLQ130210
TMEM265OVOL2Q9BRP00
TMEM265DTX3LQ8TDB60
TMEM265SCELO951710
TMEM265SH3D19Q5HYK70

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A087WTH1, A0A125YWU9, A0PK84, A6PVL3, C9JQL5, F1QHM7, F1QX91, O15503, O41933, O70418, O88728, P0DI73, P13164, P26376, Q01628, Q01629, Q08755, Q0II74, Q21642, Q32L65, Q3UNB8, Q3YBM2, Q5FVR1, Q5FWL7, Q5I0I2, Q5R8D6, Q5RF75, Q5Y5T3, Q6DHI1, Q76IC6, Q7M734, Q7TQJ1, Q8BGI3, Q8CES1, Q8CFA6, Q8IYP9, Q8N6L7, Q8WVZ1, Q91WU6, Q921C1

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

2 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

173 predictions. Top by Δscore:

VariantEffectΔscore
16:30741736:CACAG:Cacceptor_loss1.0000
16:30741739:A:AGacceptor_gain1.0000
16:30741739:AGGT:Aacceptor_gain1.0000
16:30741740:G:GGacceptor_gain1.0000
16:30741740:GGT:Gacceptor_gain1.0000
16:30741740:GGTG:Gacceptor_gain1.0000
16:30741905:CAAGG:Cdonor_loss1.0000
16:30741906:AAGG:Adonor_loss1.0000
16:30741907:AGGTG:Adonor_loss1.0000
16:30741908:GGTG:Gdonor_loss1.0000
16:30741909:G:Tdonor_loss1.0000
16:30744317:T:Aacceptor_gain1.0000
16:30744318:G:Aacceptor_gain1.0000
16:30741732:C:Aacceptor_gain0.9900
16:30741739:AG:Aacceptor_gain0.9900
16:30741740:G:GTacceptor_gain0.9900
16:30741740:GG:Gacceptor_gain0.9900
16:30741740:GGTGA:Gacceptor_gain0.9900
16:30741786:G:GTdonor_gain0.9900
16:30741879:G:GTdonor_gain0.9900
16:30741909:G:GGdonor_gain0.9900
16:30743776:CCACA:Cacceptor_loss0.9900
16:30743777:CACAG:Cacceptor_loss0.9900
16:30743779:CAGGC:Cacceptor_loss0.9900
16:30743780:A:ACacceptor_loss0.9900
16:30743780:A:AGacceptor_gain0.9900
16:30743780:AGGC:Aacceptor_gain0.9900
16:30743781:G:GCacceptor_loss0.9900
16:30743781:G:GGacceptor_gain0.9900
16:30743781:G:GTacceptor_loss0.9900

AlphaMissense

682 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:30741852:A:CS37R0.986
16:30741854:C:AS37R0.986
16:30741854:C:GS37R0.986
16:30743860:A:CS82R0.986
16:30743862:C:AS82R0.986
16:30743862:C:GS82R0.986
16:30743872:T:AW86R0.963
16:30743872:T:CW86R0.963
16:30741867:T:CC42R0.942
16:30741879:G:AG46R0.936
16:30741879:G:CG46R0.936
16:30741908:G:CK55N0.934
16:30741908:G:TK55N0.934
16:30741865:G:AG41D0.929
16:30741873:T:CC44R0.925
16:30741900:G:CA53P0.925
16:30743782:G:CA56P0.924
16:30741897:T:CF52L0.918
16:30741899:T:AF52L0.918
16:30741899:T:GF52L0.918
16:30741861:T:CC40R0.916
16:30741859:T:AI39N0.913
16:30741880:G:AG46E0.911
16:30743861:G:AS82N0.910
16:30741853:G:AS37N0.908
16:30741864:G:CG41R0.901
16:30743893:G:CG93R0.878
16:30741889:C:AA49D0.876
16:30743792:G:CR59P0.875
16:30741844:C:AA34E0.871

dbSNP variants (sampled 300 via entrez): RS1000934588 (16:30743812 G>A), RS1000965796 (16:30744080 G>A,C), RS1001305949 (16:30740134 C>T), RS1002214469 (16:30745069 C>G,T), RS1002355551 (16:30739004 T>C), RS1002948620 (16:30741180 T>G), RS1003132125 (16:30739097 C>T), RS1003426032 (16:30738861 C>T), RS1003588420 (16:30740029 A>C,G), RS1004191675 (16:30741876 C>G), RS1005868765 (16:30743129 G>A), RS1006251562 (16:30741973 T>A), RS1007028839 (16:30743450 T>G), RS1007182750 (16:30740938 G>A), RS1007871939 (16:30740552 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

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

5 total (human), top 5 by PubMed support.

ChemicalActions (top 5)PubMed papers
dicrotophosincreases expression1
abrineincreases expression1
Cadmiumdecreases expression, increases abundance1
Urethaneincreases expression1
Cadmium Chloridedecreases expression, increases abundance1

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.