TMEM267

gene
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Also known as FLJ21657

Summary

TMEM267 (transmembrane protein 267, HGNC:26139) is a protein-coding gene on chromosome 5p12, encoding Transmembrane protein 267 (Q0VDI3).

Predicted to be located in membrane.

Source: NCBI Gene 64417 — RefSeq curated summary.

At a glance

  • GWAS associations: 6
  • Clinical variants (ClinVar): 1 total
  • MANE Select transcript: NM_022483

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26139
Approved symbolTMEM267
Nametransmembrane protein 267
Location5p12
Locus typegene with protein product
StatusApproved
AliasesFLJ21657
Ensembl geneENSG00000151881
Ensembl biotypeprotein_coding
Entrez64417

Gene structure

Transcript identifiers

Ensembl transcripts: 42 — 41 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000397080, ENST00000500337, ENST00000506860, ENST00000510130, ENST00000511525, ENST00000512085, ENST00000890975, ENST00000890976, ENST00000890977, ENST00000890978, ENST00000890979, ENST00000890980, ENST00000890981, ENST00000890982, ENST00000890983, ENST00000890984, ENST00000890985, ENST00000890986, ENST00000890987, ENST00000890988, ENST00000890989, ENST00000890990, ENST00000890991, ENST00000890992, ENST00000890993, ENST00000890994, ENST00000916718, ENST00000916719, ENST00000916720, ENST00000916721, ENST00000916722, ENST00000961962, ENST00000961963, ENST00000961964, ENST00000961965, ENST00000961966, ENST00000961967, ENST00000961968, ENST00000961969, ENST00000961970, ENST00000961971, ENST00000961972

RefSeq mRNA: 11 — MANE Select: NM_022483 NM_001377394, NM_001377395, NM_001377396, NM_001377397, NM_001377398, NM_001377399, NM_001377400, NM_001377401, NM_001377402, NM_001377403, NM_022483

CCDS: CCDS3945

Canonical transcript exons

ENST00000397080 — 3 exons

ExonStartEnd
ENSE000013075504345365843454043
ENSE000019715764344425243446557
ENSE000020710424348382243483865

Expression profiles

Bgee: expression breadth ubiquitous, 239 present calls, max score 87.74.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 12.1035 / max 92.0208, expressed in 1775 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
6156410.05101746
615652.0525964

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
islet of LangerhansUBERON:000000687.74gold quality
thyroid glandUBERON:000204686.77gold quality
left lobe of thyroid glandUBERON:000112086.71gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099186.57gold quality
right lobe of thyroid glandUBERON:000111985.93gold quality
choroid plexus epitheliumUBERON:000391183.86gold quality
stromal cell of endometriumCL:000225583.72gold quality
rectumUBERON:000105282.33gold quality
calcaneal tendonUBERON:000370182.16gold quality
tibial arteryUBERON:000761082.16gold quality
popliteal arteryUBERON:000225082.15gold quality
cauda epididymisUBERON:000436082.05gold quality
palpebral conjunctivaUBERON:000181281.79gold quality
pancreasUBERON:000126481.68gold quality
corpus epididymisUBERON:000435981.65gold quality
right coronary arteryUBERON:000162581.44gold quality
caput epididymisUBERON:000435880.99gold quality
mucosa of sigmoid colonUBERON:000499380.91gold quality
aortaUBERON:000094780.88gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047380.87gold quality
bronchial epithelial cellCL:000232880.74gold quality
monocyteCL:000057680.32gold quality
leukocyteCL:000073880.19gold quality
mononuclear cellCL:000084280.17gold quality
left coronary arteryUBERON:000162680.11gold quality
minor salivary glandUBERON:000183079.99gold quality
ventricular zoneUBERON:000305379.93gold quality
endometriumUBERON:000129579.86gold quality
body of pancreasUBERON:000115079.79gold quality
pigmented layer of retinaUBERON:000178279.76gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes6.78

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

103 targeting TMEM267, 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-5692B100.0071.322622
HSA-MIR-5692C100.0071.322622
HSA-MIR-5692A100.0074.406850
HSA-MIR-4692100.0067.322066
HSA-MIR-98-3P100.0074.083907
HSA-MIR-3163100.0077.238605
HSA-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-3646100.0073.565283
HSA-MIR-4425100.0067.591049
HSA-MIR-3064-3P100.0070.091254
HSA-MIR-196A-1-3P99.9972.152772
HSA-MIR-451499.9967.101870
HSA-MIR-548AW99.9972.573559
HSA-MIR-32-5P99.9875.211964
HSA-MIR-92A-3P99.9875.211960
HSA-MIR-92B-3P99.9875.251955
HSA-MIR-25-3P99.9874.601817
HSA-MIR-363-3P99.9874.721821
HSA-MIR-367-3P99.9874.831819
HSA-MIR-477599.9875.006394
HSA-MIR-1213699.9872.815713
HSA-MIR-19A-3P99.9875.332762
HSA-MIR-19B-3P99.9875.442754
HSA-MIR-548N99.9871.944170
HSA-MIR-1468-3P99.9672.743797
HSA-MIR-590-3P99.9674.346478
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-4666A-3P99.9671.713434

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriotmem267ENSDARG00000000142
mus_musculusTmem267ENSMUSG00000074634
rattus_norvegicusTmem267ENSRNOG00000064070
drosophila_melanogasterCG10866FBGN0035475

Protein

Protein identifiers

Transmembrane protein 267Q0VDI3 (reviewed: Q0VDI3)

All UniProt accessions (3): Q0VDI3, D6RAV6, E9PBX6

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

RefSeq proteins (11): NP_001364323, NP_001364324, NP_001364325, NP_001364326, NP_001364327, NP_001364328, NP_001364329, NP_001364330, NP_001364331, NP_001364332, NP_071928* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR026572TMEM267Family

UniProt features (5 total): transmembrane region 3, chain 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q0VDI3-F189.780.74

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 88 (showing top): MODULE_205, CADWELL_ATG16L1_TARGETS_DN, COATES_MACROPHAGE_M1_VS_M2_DN, MOREAUX_MULTIPLE_MYELOMA_BY_TACI_DN, KIM_WT1_TARGETS_DN, LU_EZH2_TARGETS_DN, JOHNSTONE_PARVB_TARGETS_3_DN, TERAO_AOX4_TARGETS_SKIN_DN, SNF5_DN.V1_UP, CHAF1B_TARGET_GENES, CREB3L4_TARGET_GENES, DLX4_TARGET_GENES, DLX6_TARGET_GENES, DMRT1_TARGET_GENES, HHEX_TARGET_GENES

GO Biological Process (0):

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

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

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding1
cellular anatomical structure1

Protein interactions and networks

STRING

474 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM267PAIP1Q9H074608
TMEM267WDR70Q9NW82570
TMEM267PRXL2CQ7RTV5517
TMEM267LMBRD2Q68DH5470
TMEM267HDHD2Q9H0R4457
TMEM267C5orf34Q96MH7430
TMEM267BRIX1Q8TDN6411
TMEM267C5orf22Q49AR2397
TMEM267NADK2Q4G0N4385
TMEM267LRRC24Q50LG9381
TMEM267SPATC1Q76KD6375
TMEM267SLC15A5A6NIM6371
TMEM267LRRC14Q15048363
TMEM267SLC33A2Q96ES6363
TMEM267ADCK5Q3MIX3349

IntAct

23 interactions, top by confidence:

ABTypeScore
TMEM267CPLX4psi-mi:“MI:0915”(physical association)0.560
TMEM267TMEM52Bpsi-mi:“MI:0915”(physical association)0.560
TMEM267TMEM14Bpsi-mi:“MI:0915”(physical association)0.560
TMEM267RTP2psi-mi:“MI:0915”(physical association)0.560
STX7TMEM267psi-mi:“MI:0915”(physical association)0.560
TMEM267SAR1Apsi-mi:“MI:0915”(physical association)0.560
TMEM267ECPASpsi-mi:“MI:0914”(association)0.530
ATG16L1ESYT2psi-mi:“MI:0914”(association)0.350
TMEM267ACTA2psi-mi:“MI:0914”(association)0.350
TMEM267TMEM52Bpsi-mi:“MI:0915”(physical association)0.000
TMEM267TMEM14Bpsi-mi:“MI:0915”(physical association)0.000
RTP2TMEM267psi-mi:“MI:0915”(physical association)0.000
STX7TMEM267psi-mi:“MI:0915”(physical association)0.000
TMEM267SAR1Apsi-mi:“MI:0915”(physical association)0.000
TMEM267CPLX4psi-mi:“MI:0915”(physical association)0.000

BioGRID (17): C5orf28 (Affinity Capture-MS), LNPEP (Affinity Capture-MS), KIAA0368 (Affinity Capture-MS), PTGES2 (Affinity Capture-MS), C5orf28 (Two-hybrid), C5orf28 (Two-hybrid), C5orf28 (Two-hybrid), C5orf28 (Two-hybrid), TMEM52B (Two-hybrid), CPLX4 (Two-hybrid), RTP2 (Two-hybrid), C5orf28 (Affinity Capture-RNA), KIAA0368 (Affinity Capture-MS), LNPEP (Affinity Capture-MS), ACTA2 (Affinity Capture-MS)

ESM2 similar proteins: A0A1B0GVZ9, A4IFN5, A5PK40, A6NH52, A6NI61, B2LYG4, B2RZC9, B6ID01, D2HKB0, D3ZG27, P86229, Q0VDI3, Q15012, Q15546, Q17QJ2, Q1RLT2, Q2TA01, Q4R4I5, Q4R6E8, Q5H8A4, Q5R7Q1, Q5RAH0, Q5RL79, Q5U3C3, Q5VTY9, Q5ZML7, Q64232, Q6PHN7, Q6QRN8, Q719N3, Q71SV0, Q8BWB6, Q8IY49, Q8N6M3, Q8NFT2, Q8R189, Q8VD53, Q8VDI9, Q8VDR5, Q9CQC4

Diamond homologs: Q0VDI3, Q17QJ2, Q6DC75, Q6DED9, Q8VDR5

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

1 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

938 predictions. Top by Δscore:

VariantEffectΔscore
5:43454493:T:Cdonor_gain0.9900
5:43454531:T:TAdonor_gain0.9900
5:43454536:T:Adonor_gain0.9800
5:43457001:A:Cacceptor_gain0.9700
5:43483438:CAA:Cdonor_gain0.9700
5:43479864:C:CTacceptor_gain0.9500
5:43483436:TACA:Tdonor_gain0.9500
5:43483437:ACAA:Adonor_gain0.9500
5:43483438:CAAC:Cdonor_gain0.9500
5:43481807:C:Tacceptor_gain0.9400
5:43483439:A:ATdonor_gain0.9400
5:43446554:CAGC:Cacceptor_gain0.9300
5:43446558:C:CCacceptor_gain0.9200
5:43483820:ACC:Adonor_gain0.9100
5:43483821:CCC:Cdonor_gain0.9100
5:43483736:T:TAdonor_gain0.9000
5:43483820:AC:Adonor_gain0.8900
5:43483821:CC:Cdonor_gain0.8900
5:43481807:C:CTacceptor_gain0.8600
5:43483787:C:Adonor_gain0.8600
5:43480091:G:Cdonor_gain0.8400
5:43483814:ATAC:Adonor_loss0.8300
5:43483816:ACCC:Adonor_loss0.8300
5:43483818:CCACC:Cdonor_loss0.8300
5:43483819:CA:Cdonor_loss0.8300
5:43483820:A:AGdonor_loss0.8300
5:43483821:C:CGdonor_loss0.8300
5:43483815:TAC:Tdonor_loss0.8200
5:43457001:A:ACacceptor_gain0.8000
5:43483304:T:TAdonor_gain0.8000

AlphaMissense

1392 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
5:43446397:C:GR158P0.990
5:43453783:A:GW63R0.990
5:43453783:A:TW63R0.990
5:43446407:G:CH155D0.989
5:43453777:A:GW65R0.987
5:43453777:A:TW65R0.987
5:43446524:G:CH116D0.986
5:43446394:T:AD159V0.985
5:43453698:T:AD91V0.982
5:43446393:A:CD159E0.981
5:43446393:A:TD159E0.981
5:43446395:C:GD159H0.981
5:43446405:A:CH155Q0.981
5:43446405:A:TH155Q0.981
5:43453719:C:TG84E0.981
5:43446394:T:GD159A0.980
5:43453697:A:CD91E0.980
5:43453697:A:TD91E0.980
5:43453720:C:GG84R0.980
5:43453720:C:TG84R0.980
5:43446416:A:GW152R0.979
5:43446416:A:TW152R0.979
5:43453692:T:AD93V0.979
5:43453788:C:TG61D0.978
5:43453801:G:CH57D0.976
5:43453808:A:CN54K0.976
5:43453808:A:TN54K0.976
5:43453688:G:CH94Q0.975
5:43453688:G:TH94Q0.975
5:43453698:T:GD91A0.975

dbSNP variants (sampled 300 via entrez): RS1000004093 (5:43447999 T>G), RS1000066304 (5:43486038 C>G), RS1000131860 (5:43444850 T>C), RS1000159651 (5:43454359 G>A), RS1000201060 (5:43456755 G>T), RS1000263726 (5:43447622 C>T), RS1000311257 (5:43460354 C>T), RS1000377674 (5:43478753 T>C,G), RS1000414316 (5:43463316 A>G), RS1000550329 (5:43463082 T>C,G), RS1000663867 (5:43457590 A>G), RS1000750983 (5:43474113 C>A,T), RS1000795894 (5:43486232 G>A), RS1000845432 (5:43481680 C>T), RS1000867403 (5:43454031 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

6 associations (top):

StudyTraitp-value
GCST003265_377Post bronchodilator FEV1/FVC ratio in COPD2.000000e-06
GCST003265_378Post bronchodilator FEV1/FVC ratio in COPD2.000000e-06
GCST003265_379Post bronchodilator FEV1/FVC ratio in COPD2.000000e-06
GCST003265_394Post bronchodilator FEV1/FVC ratio in COPD2.000000e-06
GCST003265_395Post bronchodilator FEV1/FVC ratio in COPD2.000000e-06
GCST003265_396Post bronchodilator FEV1/FVC ratio in COPD2.000000e-06

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004713FEV/FVC ratio

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

33 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects cotreatment, decreases expression, affects expression7
Cyclosporineincreases expression3
sodium arseniteaffects cotreatment, increases abundance, increases expression, decreases expression2
methylmercuric chloridedecreases expression1
cobaltous chloridedecreases expression1
potassium chromate(VI)affects cotreatment, decreases expression1
aflatoxin B2increases methylation1
epigallocatechin gallateaffects cotreatment, decreases expression1
di-n-butylphosphoric acidaffects expression1
perfluoro-n-nonanoic acidincreases expression1
entinostatdecreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
abrinedecreases expression1
dorsomorphinaffects cotreatment, decreases expression1
jinfukangdecreases expression1
4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acidincreases expression1
Irinotecandecreases expression1
Sunitinibincreases expression1
Zoledronic Acidincreases expression1
Arsenic Trioxideincreases expression1
Acetaminophendecreases expression1
Arsenicaffects cotreatment, increases abundance, increases expression, decreases expression1
Hexachlorocyclohexaneincreases expression1
Benzo(a)pyrenedecreases expression1
Cyclophosphamidedecreases expression1
Formaldehydeincreases expression1
Tobacco Smoke Pollutionincreases expression1
Tretinoindecreases expression1
Vincristineincreases expression1
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxidedecreases 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.