TMEM156

gene
On this page

Also known as FLJ23235

Summary

TMEM156 (transmembrane protein 156, HGNC:26260) is a protein-coding gene on chromosome 4p14, encoding Transmembrane protein 156 (Q8N614).

Predicted to be located in membrane.

Source: NCBI Gene 80008 — RefSeq curated summary.

At a glance

  • GWAS associations: 6
  • Clinical variants (ClinVar): 49 total
  • MANE Select transcript: NM_024943

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26260
Approved symbolTMEM156
Nametransmembrane protein 156
Location4p14
Locus typegene with protein product
StatusApproved
AliasesFLJ23235
Ensembl geneENSG00000121895
Ensembl biotypeprotein_coding
Entrez80008

Gene structure

Transcript identifiers

Ensembl transcripts: 9 — 7 protein_coding, 2 protein_coding_CDS_not_defined

ENST00000344606, ENST00000372489, ENST00000381938, ENST00000495029, ENST00000850870, ENST00000877062, ENST00000877063, ENST00000877064, ENST00000877065

RefSeq mRNA: 2 — MANE Select: NM_024943 NM_001303228, NM_024943

CCDS: CCDS3448

Canonical transcript exons

ENST00000381938 — 7 exons

ExonStartEnd
ENSE000008264363898633638986419
ENSE000008264373898885138988970
ENSE000008264383899373838993998
ENSE000008264393899864038998909
ENSE000010771833897103238971137
ENSE000014903413903222639032409
ENSE000042825763896674438967641

Expression profiles

Bgee: expression breadth ubiquitous, 175 present calls, max score 97.05.

FANTOM5 (CAGE): breadth broad, TPM avg 4.2234 / max 211.8160, expressed in 570 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
518214.0731555
518220.096653
518230.053718

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
buccal mucosa cellCL:000233697.05gold quality
granulocyteCL:000009486.98gold quality
lymph nodeUBERON:000002985.10gold quality
spleenUBERON:000210683.94gold quality
bone marrow cellCL:000209282.73gold quality
vermiform appendixUBERON:000115480.58gold quality
colonic epitheliumUBERON:000039776.37gold quality
caecumUBERON:000115375.93gold quality
bone marrowUBERON:000237175.40gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047374.36gold quality
bloodUBERON:000017873.81gold quality
superficial temporal arteryUBERON:000161472.54gold quality
tonsilUBERON:000237272.51gold quality
rectumUBERON:000105272.44gold quality
small intestine Peyer’s patchUBERON:000345472.39gold quality
C1 segment of cervical spinal cordUBERON:000646972.19gold quality
leukocyteCL:000073872.17gold quality
monocyteCL:000057671.11gold quality
mononuclear cellCL:000084270.92gold quality
mucosa of transverse colonUBERON:000499170.43gold quality
gall bladderUBERON:000211069.88gold quality
spinal cordUBERON:000224069.26gold quality
small intestineUBERON:000210869.03gold quality
epithelium of nasopharynxUBERON:000195168.84gold quality
adrenal tissueUBERON:001830365.56gold quality
parotid glandUBERON:000183164.50gold quality
transverse colonUBERON:000115761.85gold quality
substantia nigraUBERON:000203861.72gold quality
right lobe of liverUBERON:000111461.68gold quality
skeletal muscle tissue of rectus abdominisUBERON:000451161.20gold quality

Single-cell (SCXA)

Detected in 4 experiment(s), a significant marker in 3.

ExperimentMarker?Max mean expression
E-MTAB-8142yes22.87
E-ANND-3yes13.36
E-MTAB-10553yes8.77
E-CURD-112no2.86

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

46 targeting TMEM156, 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-5692A100.0074.406850
HSA-MIR-495-3P99.9672.814197
HSA-MIR-568899.9673.234504
HSA-MIR-335-3P99.9373.364958
HSA-MIR-449699.8868.892236
HSA-MIR-659-3P99.8570.691620
HSA-MIR-5010-3P99.8370.602357
HSA-MIR-204-5P99.7971.622439
HSA-MIR-211-5P99.7971.652440
HSA-MIR-62399.7668.161170
HSA-MIR-4524A-3P99.7266.852406
HSA-MIR-4755-5P99.7170.342716
HSA-MIR-5006-3P99.7170.262728
HSA-MIR-1212499.6869.172700
HSA-MIR-548AV-5P99.6070.842107
HSA-MIR-548K99.6070.842107
HSA-MIR-426199.5970.303415
HSA-MIR-431099.5968.842527
HSA-MIR-3136-3P99.5766.59781
HSA-MIR-7155-3P99.5766.48794
HSA-MIR-6758-3P99.5767.551078
HSA-MIR-6832-3P99.5270.441726
HSA-MIR-6727-3P99.4965.921333
HSA-MIR-805499.4870.812084
HSA-MIR-147B-5P99.4570.622432
HSA-MIR-4999-5P99.3569.15926
HSA-MIR-4722-3P99.3565.221099
HSA-MIR-6744-3P99.2264.41972
HSA-MIR-6780B-3P99.1367.18622
HSA-MIR-4757-5P99.1264.51981

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusTmem156ENSMUSG00000037913
rattus_norvegicusTmem156ENSRNOG00000026518

Protein

Protein identifiers

Transmembrane protein 156Q8N614 (reviewed: Q8N614)

All UniProt accessions (2): J3KNV8, Q8N614

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

RefSeq proteins (2): NP_001290157, NP_079219* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR029374TMEM156Family

Pfam: PF15106

UniProt features (11 total): topological domain 3, sequence variant 3, transmembrane region 2, glycosylation site 2, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8N614-F143.220.00

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 (2): 45, 156

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 96 (showing top): IVANOVA_HEMATOPOIESIS_LATE_PROGENITOR, ODONNELL_TARGETS_OF_MYC_AND_TFRC_UP, TGANTCA_AP1_C, SENESE_HDAC1_TARGETS_UP, FOXJ2_02, CERVERA_SDHB_TARGETS_1_UP, MODULE_277, AP1FJ_Q2, LEE_RECENT_THYMIC_EMIGRANT, MGGAAGTG_GABP_B, MISHRA_CARCINOMA_ASSOCIATED_FIBROBLAST_UP, TCANNTGAY_SREBP1_01, DODD_NASOPHARYNGEAL_CARCINOMA_DN, AP1_Q6_01, PEDERSEN_METASTASIS_BY_ERBB2_ISOFORM_7

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

598 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM156KLHL5Q96PQ7636
TMEM156RFC1P35251576
TMEM156RPL9P32969522
TMEM156LIASO43766514
TMEM156SMIM14Q96QK8508
TMEM156WDR19Q8NEZ3504
TMEM156RBM47A0AV96467
TMEM156ASZ1Q8WWH4460
TMEM156N4BP2Q86UW6453
TMEM156LRRC66Q68CR7435
TMEM156PDS5AQ29RF7427
TMEM156KLF3P57682425
TMEM156TLR10Q9BXR5424
TMEM156UBE2KP27924414
TMEM156APBB2Q92870412

IntAct

4 interactions, top by confidence:

ABTypeScore
SHTN1psi-mi:“MI:0914”(association)0.350
TMEM223psi-mi:“MI:0914”(association)0.350

BioGRID (6): TMEM156 (Affinity Capture-MS), TMEM156 (Affinity Capture-MS), TMEM156 (Affinity Capture-MS), TMEM156 (Proximity Label-MS), TMEM156 (Proximity Label-MS), TMEM156 (Protein-peptide)

ESM2 similar proteins: A0A1B0GTR0, A0A1B0GTY4, A0A1B0GVD1, A7WNB0, A8R0V4, E9Q7F5, O55779, O70552, O75818, O93036, P01586, P03212, P03319, P03321, P04823, P0DOE0, P10260, P13206, P16837, P20880, P28907, P36340, P47939, P47940, Q02484, Q03233, Q1HVF6, Q2HRD2, Q3KSS3, Q3TTJ4, Q5BK38, Q5QR91, Q5VAN0, Q64277, Q66669, Q66672, Q6GQU0, Q6GVM5, Q6UWF9, Q86WR6

Diamond homologs: Q5BK38, Q8N614

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance39
Likely benign5
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1423 predictions. Top by Δscore:

VariantEffectΔscore
4:38967649:T:TCacceptor_gain1.0000
4:38967650:T:Cacceptor_gain1.0000
4:38971133:CTCTG:Cacceptor_gain1.0000
4:38971138:C:CCacceptor_gain1.0000
4:38993999:C:CCacceptor_gain1.0000
4:38967638:TATT:Tacceptor_gain0.9900
4:38967640:TTC:Tacceptor_loss0.9900
4:38967641:TC:Tacceptor_loss0.9900
4:38967642:C:CCacceptor_gain0.9900
4:38967642:CTGA:Cacceptor_loss0.9900
4:38967650:T:TCacceptor_gain0.9900
4:38967654:A:ACacceptor_gain0.9900
4:38971025:CACT:Cdonor_loss0.9900
4:38971026:ACTC:Adonor_loss0.9900
4:38971027:CT:Cdonor_loss0.9900
4:38971028:T:TAdonor_loss0.9900
4:38971029:C:CGdonor_loss0.9900
4:38971030:ACC:Adonor_loss0.9900
4:38971135:CTG:Cacceptor_gain0.9900
4:38971136:TG:Tacceptor_gain0.9900
4:38986417:GACC:Gacceptor_loss0.9900
4:38986418:ACC:Aacceptor_loss0.9900
4:38986421:T:Gacceptor_loss0.9900
4:38986427:C:Tacceptor_gain0.9900
4:38988849:A:ACdonor_gain0.9900
4:38988850:C:CCdonor_gain0.9900
4:38988850:CT:Cdonor_gain0.9900
4:38988850:CTCTG:Cdonor_gain0.9900
4:38993736:A:ACdonor_gain0.9900
4:38993737:C:CCdonor_gain0.9900

AlphaMissense

1956 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
4:38988944:A:GW216R0.937
4:38988944:A:TW216R0.937
4:38998889:A:GC37R0.903
4:39032239:G:CF25L0.893
4:39032239:G:TF25L0.893
4:39032241:A:GF25L0.893
4:38998691:A:GC103R0.864
4:38998887:A:CC37W0.853
4:39032290:T:AK8N0.853
4:39032290:T:GK8N0.853
4:38998690:C:GC103S0.842
4:38998691:A:TC103S0.842
4:38998888:C:GC37S0.841
4:38998889:A:TC37S0.841
4:39032279:G:TA12E0.841
4:39032267:G:TT16K0.823
4:38998888:C:TC37Y0.800
4:38998690:C:TC103Y0.792
4:38998894:A:GL35P0.783
4:38998689:A:CC103W0.755
4:38988918:A:CF224L0.754
4:38988918:A:TF224L0.754
4:38988920:A:GF224L0.754
4:39032276:A:TI13K0.753
4:38988931:A:TV220D0.751
4:39032267:G:CT16R0.751
4:38988942:C:AW216C0.740
4:38988942:C:GW216C0.740
4:39032249:G:TP22Q0.731
4:39032292:T:CK8E0.728

dbSNP variants (sampled 300 via entrez): RS1000032425 (4:39008669 A>C), RS1000040262 (4:38984521 G>A,T), RS10001298 (4:39005146 C>G,T), RS1000140782 (4:39019692 ATTATATATATAT>A), RS1000146074 (4:39031776 C>T), RS1000187432 (4:38978738 T>A), RS1000187892 (4:38980204 A>C), RS1000255284 (4:38983341 G>A,C), RS1000347136 (4:38971938 C>A), RS1000371390 (4:39019256 T>C), RS10003755 (4:38966352 T>C,G), RS1000397350 (4:39025453 C>G,T), RS1000408947 (4:38973747 G>T), RS1000423415 (4:38989863 G>A), RS1000435074 (4:38984337 C>G)

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
GCST012490_624Femur bone mineral density x serum urate levels interaction7.000000e-09
GCST012490_71Femur bone mineral density x serum urate levels interaction9.000000e-11
GCST90002381_205Eosinophil count3.000000e-18
GCST90002382_595Eosinophil percentage of white cells2.000000e-13
GCST90002393_220Monocyte count8.000000e-25
GCST90002394_54Monocyte percentage of white cells2.000000e-15

EFO canonical traits (5, from GWAS)

EFO IDTrait name
EFO:0004531urate measurement
EFO:0004842eosinophil count
EFO:0007991eosinophil percentage of leukocytes
EFO:0005091monocyte count
EFO:0007989monocyte percentage of leukocytes

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
Tetrachlorodibenzodioxinaffects cotreatment, decreases expression, increases expression4
Particulate Matterincreases expression, increases abundance4
(+)-JQ1 compounddecreases expression, affects cotreatment3
Benzo(a)pyreneaffects methylation, increases expression3
sodium arseniteincreases expression2
Air Pollutantsincreases abundance, increases expression2
Silicon Dioxideincreases expression2
Smokeincreases expression2
Aflatoxin B1increases methylation, increases expression2
sotorasibaffects cotreatment, decreases expression1
methyleugenolincreases expression1
triphenyl phosphateaffects expression1
2-methyl-4-isothiazolin-3-oneincreases expression1
hydroxyhydroquinoneincreases expression1
methylparabendecreases expression1
sulforaphaneincreases expression1
tris(1,3-dichloro-2-propyl)phosphateincreases expression1
didecyldimethylammoniumincreases expression1
potassium chromate(VI)decreases expression1
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression, affects cotreatment, decreases expression1
di-n-butylphosphoric acidaffects expression1
perfluorooctane sulfonic acidincreases expression1
perfluoro-n-nonanoic acidincreases expression1
2-palmitoylglycerolincreases expression1
abrineincreases expression1
mirdametinibaffects cotreatment, decreases expression1
2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amideaffects cotreatment, decreases expression1
bisphenol Saffects cotreatment, increases methylation1
jinfukangdecreases expression1
NSC 689534affects binding, increases 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.