TMEM236

gene
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Also known as bA16O1.2bA162I21.2

Summary

TMEM236 (transmembrane protein 236, HGNC:23473) is a protein-coding gene on chromosome 10p12.33, encoding Transmembrane protein 236 (Q5W0B7).

Predicted to be located in membrane.

Source: NCBI Gene 653567 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 6 total
  • MANE Select transcript: NM_001098844

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:23473
Approved symbolTMEM236
Nametransmembrane protein 236
Location10p12.33
Locus typegene with protein product
StatusApproved
AliasesbA16O1.2, bA162I21.2
Ensembl geneENSG00000148483
Ensembl biotypeprotein_coding
Entrez653567

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000377495

RefSeq mRNA: 1 — MANE Select: NM_001098844 NM_001098844

CCDS: CCDS41492

Canonical transcript exons

ENST00000377495 — 4 exons

ExonStartEnd
ENSE000024364081779592117800868
ENSE000024374311777602917776170
ENSE000024471191777130917771381
ENSE000024497231775220117752552

Expression profiles

Bgee: expression breadth broad, 89 present calls, max score 88.66.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.7294 / max 175.3422, expressed in 131 samples.

FANTOM5 promoters (5 alternative TSS)

Promoter IDTPM avgSamples expressed
2057500.4183116
2057440.253812
2057490.036414
2057450.01637
2057430.00464

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
duodenumUBERON:000211488.66gold quality
rectumUBERON:000105284.88gold quality
islet of LangerhansUBERON:000000684.26gold quality
mucosa of transverse colonUBERON:000499182.75gold quality
small intestineUBERON:000210875.46gold quality
transverse colonUBERON:000115775.19gold quality
small intestine Peyer’s patchUBERON:000345474.74gold quality
intestineUBERON:000016068.70gold quality
placentaUBERON:000198766.12gold quality
colonUBERON:000115565.95gold quality
colonic epitheliumUBERON:000039765.91silver quality
vermiform appendixUBERON:000115465.48gold quality
smooth muscle tissueUBERON:000113564.59gold quality
pancreasUBERON:000126462.77gold quality
right lungUBERON:000216757.68gold quality
right adrenal gland cortexUBERON:003582756.87gold quality
subcutaneous adipose tissueUBERON:000219056.82gold quality
muscle tissueUBERON:000238556.62gold quality
upper lobe of left lungUBERON:000895255.23gold quality
bone marrow cellCL:000209255.20gold quality
adipose tissueUBERON:000101355.03gold quality
right adrenal glandUBERON:000123354.59gold quality
left adrenal glandUBERON:000123454.41gold quality
skeletal muscle tissueUBERON:000113454.39silver quality
left adrenal gland cortexUBERON:003582553.70gold quality
mucosa of stomachUBERON:000119953.68gold quality
adrenal glandUBERON:000236953.68gold quality
lungUBERON:000204853.15gold quality
right coronary arteryUBERON:000162552.99gold quality
gastrocnemiusUBERON:000138852.94gold quality

Single-cell (SCXA)

Detected in 6 experiment(s), a significant marker in 6.

ExperimentMarker?Max mean expression
E-GEOD-83139yes242.13
E-GEOD-81608yes206.86
E-ENAD-27yes164.24
E-MTAB-5061yes32.11
E-GEOD-81547yes20.32
E-ANND-3yes4.40

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

140 targeting TMEM236, 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-3163100.0077.238605
HSA-MIR-29A-3P100.0073.111835
HSA-MIR-29B-3P100.0073.181833
HSA-MIR-29C-3P100.0073.151833
HSA-MIR-3646100.0073.565283
HSA-MIR-5011-5P100.0083.465820
HSA-MIR-3064-3P100.0070.091254
HSA-MIR-3613-3P100.0076.367965
HSA-MIR-1277-5P100.0073.955056
HSA-MIR-340-5P100.0072.504437
HSA-MIR-190A-3P100.0080.355520
HSA-MIR-428299.9975.366408
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-186-5P99.9970.833707
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-4789-3P99.9970.752484
HSA-MIR-477599.9875.006394
HSA-MIR-1213699.9872.815713
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-548N99.9871.944170
HSA-MIR-60799.9773.625593
HSA-MIR-590-3P99.9674.346478
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-767-5P99.9570.85993
HSA-MIR-9983-3P99.9471.483631
HSA-MIR-311999.9271.342390
HSA-MIR-652-5P99.9167.49505
HSA-MIR-129799.9173.413162
HSA-MIR-454-3P99.9174.011925

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriotmem236ENSDARG00000075715
mus_musculusTmem236ENSMUSG00000061531
rattus_norvegicusTmem236ENSRNOG00000037982

Protein

Protein identifiers

Transmembrane protein 236Q5W0B7 (reviewed: Q5W0B7)

All UniProt accessions (1): Q5W0B7

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the TMEM236 family.

RefSeq proteins (1): NP_001092314* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR020394Uncharacterised_FAM23-like_TMFamily

UniProt features (10 total): transmembrane region 6, chain 1, region of interest 1, compositionally biased region 1, glycosylation site 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q5W0B7-F173.710.20

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 (1): 193

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 43 (showing top): chr10p12, ZFP91_TARGET_GENES, MIR153_5P, MIR12136, MIR3646, MIR4659A_3P_MIR4659B_3P, MIR95_5P, MIR548AR_3P, MIR548F_3P, MIR548BC, MIR548AZ_3P, MIR548A_3P, MIR4495, MIR548E_3P, MIR944

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

300 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM236TXLNBQ8N3L3627
TMEM236CCDC158Q5M9N0531
TMEM236IQSEC3Q9UPP2510
TMEM236OR13C8Q8NGS7504
TMEM236LRRC14BA6NHZ5499
TMEM236TMEM191BP0C7N4476
TMEM236CALN1Q9BXU9471
TMEM236IGSF5Q9NSI5469
TMEM236RBMS3Q6XE24463
TMEM236ZFYVE26Q68DK2459
TMEM236PRPF6O94906448
TMEM236KCTD16Q68DU8448
TMEM236FAM47BQ8NA70444
TMEM236TTC9Q92623437
TMEM236TMEM179BQ7Z7N9435

IntAct

18 interactions, top by confidence:

ABTypeScore
OPRM1TMEM236psi-mi:“MI:0915”(physical association)0.560
TMEM236TMEM179Bpsi-mi:“MI:0915”(physical association)0.560
AQP2TMEM236psi-mi:“MI:0915”(physical association)0.560
TMEM236GPR152psi-mi:“MI:0915”(physical association)0.560
FAM209ATMEM236psi-mi:“MI:0915”(physical association)0.560
TMEM236SHBGpsi-mi:“MI:0915”(physical association)0.400
TMEM236OPRM1psi-mi:“MI:0915”(physical association)0.000
TMEM236AQP2psi-mi:“MI:0915”(physical association)0.000
TMEM236GPR152psi-mi:“MI:0915”(physical association)0.000
TMEM236FAM209Apsi-mi:“MI:0915”(physical association)0.000
TMEM236TMEM179Bpsi-mi:“MI:0915”(physical association)0.000

BioGRID (7): SHBG (Affinity Capture-MS), TMEM236 (Two-hybrid), TMEM236 (Two-hybrid), AQP2 (Two-hybrid), GPR152 (Two-hybrid), TMEM179B (Two-hybrid), SHBG (Affinity Capture-MS)

ESM2 similar proteins: A0A0R4IDX9, A0A2C9VBV6, A2ARJ3, A7T1N0, A7Y2X0, A8Y2U2, O12977, O17386, O35119, O70131, O76689, O80739, P31662, P52166, P70617, P79100, Q05005, Q08469, Q0WMJ8, Q3UP23, Q57UM0, Q5JK32, Q5R9C2, Q5W0B7, Q69RI8, Q6H4R6, Q6NPT7, Q6ZUK4, Q75G84, Q84MS3, Q84MS4, Q8BG16, Q8BJI1, Q8MPP0, Q90X07, Q92982, Q94KB1, Q94KB9, Q9FI00, Q9FY75

Diamond homologs: A2ARJ3, A5WVU6, Q05005, Q5W0B7

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance4
Likely benign1
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

1259 predictions. Top by Δscore:

VariantEffectΔscore
10:17775765:G:GTdonor_gain1.0000
10:17776166:AAAGA:Adonor_gain1.0000
10:17776167:AAGA:Adonor_gain1.0000
10:17776167:AAGAG:Adonor_loss1.0000
10:17776168:AGA:Adonor_gain1.0000
10:17776168:AGAGT:Adonor_loss1.0000
10:17776169:GA:Gdonor_gain1.0000
10:17776169:GAG:Gdonor_gain1.0000
10:17776169:GAGTA:Gdonor_loss1.0000
10:17776171:G:Cdonor_loss1.0000
10:17776171:G:GGdonor_gain1.0000
10:17776172:TAAG:Tdonor_loss1.0000
10:17752548:GGATG:Gdonor_gain0.9900
10:17752549:GATG:Gdonor_gain0.9900
10:17752549:GATGG:Gdonor_gain0.9900
10:17752550:ATGGT:Adonor_loss0.9900
10:17752551:TGGTA:Tdonor_loss0.9900
10:17752553:G:Cdonor_loss0.9900
10:17752554:T:Gdonor_loss0.9900
10:17776024:AACAG:Aacceptor_loss0.9900
10:17776025:ACAGG:Aacceptor_loss0.9900
10:17776026:CAGG:Cacceptor_loss0.9900
10:17776027:A:AGacceptor_gain0.9900
10:17776028:G:GGacceptor_gain0.9900
10:17776159:G:GTdonor_gain0.9900
10:17776173:AAGT:Adonor_loss0.9900
10:17778778:C:Gdonor_gain0.9900
10:17795920:GGTA:Gacceptor_gain0.9900
10:17752551:TG:Tdonor_gain0.9800
10:17752552:GG:Gdonor_gain0.9800

AlphaMissense

2273 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
10:17796265:A:CS273R0.996
10:17796267:T:AS273R0.996
10:17796267:T:GS273R0.996
10:17796416:A:TK323I0.994
10:17796181:T:AW245R0.992
10:17796181:T:CW245R0.992
10:17796417:A:CK323N0.992
10:17796417:A:TK323N0.992
10:17796420:T:AN324K0.991
10:17796420:T:GN324K0.991
10:17796241:T:AW265R0.989
10:17796241:T:CW265R0.989
10:17752491:T:AW66R0.988
10:17752491:T:CW66R0.988
10:17796349:T:CF301L0.988
10:17796351:C:AF301L0.988
10:17796351:C:GF301L0.988
10:17752390:C:AA32D0.985
10:17796362:G:CR305T0.985
10:17796188:A:TD247V0.983
10:17796187:G:CD247H0.982
10:17796206:G:CR253P0.982
10:17796448:T:CF334L0.982
10:17796450:C:AF334L0.982
10:17796450:C:GF334L0.982
10:17796347:C:GP300R0.981
10:17796188:A:CD247A0.980
10:17796363:A:CR305S0.980
10:17796363:A:TR305S0.980
10:17796200:T:GM251R0.979

dbSNP variants (sampled 300 via entrez): RS1000055894 (10:17789676 T>C), RS1000066599 (10:17754347 G>A,T), RS1000114971 (10:17795114 G>A), RS1000120957 (10:17779550 A>C,G), RS1000213065 (10:17764508 A>G), RS1000233896 (10:17794883 C>G), RS1000244423 (10:17764795 C>T), RS1000296887 (10:17800369 T>G), RS1000343465 (10:17789845 C>A,T), RS1000408613 (10:17789426 A>T), RS1000486890 (10:17770063 A>G,T), RS1000541186 (10:17759840 G>T), RS1000600085 (10:17759414 C>G), RS1000610728 (10:17774975 A>G), RS1000641938 (10:17775279 T>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

2 associations (top):

StudyTraitp-value
GCST000583_17Hematological and biochemical traits1.000000e-16
GCST007732_14Allergic disease (asthma, hay fever or eczema)7.000000e-07

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004736aspartate aminotransferase measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

15 total (human), top 15 by PubMed support.

ChemicalActions (top 5)PubMed papers
aristolochic acid Iincreases expression1
sotorasibdecreases expression, affects cotreatment1
bisphenol Adecreases expression1
butyraldehydeincreases expression1
perfluorooctanoic aciddecreases expression1
ferrous chlorideincreases expression1
abrineincreases expression1
trametinibaffects cotreatment, decreases expression1
NVP-BKM120affects cotreatment, decreases expression1
ortho-topolin ribosideaffects cotreatment, decreases expression1
Melatoninaffects cotreatment, decreases expression1
Thiramincreases expression1
Aflatoxin B1increases methylation1
Okadaic Acidincreases expression1
Magnetite Nanoparticlesincreases 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.