TMEM202

gene
On this page

Also known as FLJ27523

Summary

TMEM202 (transmembrane protein 202, HGNC:33733) is a protein-coding gene on chromosome 15q23-q24.1, encoding Transmembrane protein 202 (A6NGA9).

Predicted to be located in membrane. Predicted to be active in plasma membrane.

Source: NCBI Gene 338949 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 36 total
  • MANE Select transcript: NM_001080462

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:33733
Approved symbolTMEM202
Nametransmembrane protein 202
Location15q23-q24.1
Locus typegene with protein product
StatusApproved
AliasesFLJ27523
Ensembl geneENSG00000187806
Ensembl biotypeprotein_coding
Entrez338949

Gene structure

Transcript identifiers

Ensembl transcripts: 4 — 3 protein_coding, 1 nonsense_mediated_decay

ENST00000341689, ENST00000567679, ENST00000568167, ENST00000649825

RefSeq mRNA: 1 — MANE Select: NM_001080462 NM_001080462

CCDS: CCDS32287

Canonical transcript exons

ENST00000341689 — 5 exons

ExonStartEnd
ENSE000013663927239865372398908
ENSE000025775377239830572398407
ENSE000034636697240660272406751
ENSE000035211497240769172408367
ENSE000036603387240708672407217

Expression profiles

Bgee: expression breadth broad, 23 present calls, max score 94.76.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0236 / max 23.0053, expressed in 3 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1475770.02363

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047394.76gold quality
left testisUBERON:000453385.94gold quality
testisUBERON:000047385.41gold quality
right testisUBERON:000453484.32gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099178.55gold quality
quadriceps femorisUBERON:000137777.26gold quality
thymusUBERON:000237056.63silver quality
hindlimb stylopod muscleUBERON:000425240.84gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
sural nerveUBERON:001548836.26gold quality
bone marrow cellCL:000209236.16gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113433.70gold quality
monocyteCL:000057632.22gold quality
bone marrowUBERON:000237132.02gold quality
leukocyteCL:000073831.80gold quality
muscle tissueUBERON:000238531.31gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.85gold quality
liverUBERON:000210729.37gold quality
ectocervixUBERON:001224928.45silver quality
duodenumUBERON:000211428.14gold quality
placentaUBERON:000198728.05silver quality
superior frontal gyrusUBERON:000266127.69gold quality
lymph nodeUBERON:000002927.57gold quality
bloodUBERON:000017827.52silver quality
tonsilUBERON:000237227.05gold quality
vermiform appendixUBERON:000115426.42gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.94

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

26 targeting TMEM202, 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-499A-5P99.9870.791323
HSA-MIR-7152-3P99.9767.47849
HSA-MIR-365899.9673.874379
HSA-MIR-568099.9169.833421
HSA-MIR-129799.9173.413162
HSA-MIR-807699.7868.521170
HSA-MIR-3617-5P99.7569.411968
HSA-MIR-64199.7569.351975
HSA-MIR-4699-3P99.7170.153142
HSA-MIR-7159-5P99.5372.122472
HSA-MIR-155-5P99.3570.161509
HSA-MIR-427999.1966.702437
HSA-MIR-5583-3P99.0665.681018
HSA-MIR-10B-3P99.0466.98988
HSA-MIR-42198.9067.041883
HSA-MIR-3145-3P98.8569.072031
HSA-MIR-797798.6566.182590
HSA-MIR-4709-5P98.5167.251335
HSA-MIR-449098.5168.47943
HSA-MIR-6801-3P98.0464.64805
HSA-MIR-6810-3P97.9664.571023
HSA-MIR-5000-5P97.4066.111055
HSA-MIR-3663-5P97.0164.84713
HSA-MIR-10525-3P96.3268.04699
HSA-MIR-208A-3P95.8766.51397
HSA-MIR-208B-3P95.8766.56396

Cross-species orthologs

0 orthologs

Paralogs (10): LIM2 (ENSG00000105370), NKG7 (ENSG00000105374), PMP22 (ENSG00000109099), GSG1 (ENSG00000111305), EMP1 (ENSG00000134531), EMP3 (ENSG00000142227), CLDND2 (ENSG00000160318), GSG1L (ENSG00000169181), EMP2 (ENSG00000213853), GSG1L2 (ENSG00000214978)

Protein

Protein identifiers

Transmembrane protein 202A6NGA9 (reviewed: A6NGA9)

All UniProt accessions (3): A6NGA9, A0A3B3ITB0, H3BUG9

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

RefSeq proteins (1): NP_001073931* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR050579PMP-22/EMP/MP20-likeFamily

UniProt features (8 total): transmembrane region 4, chain 1, region of interest 1, compositionally biased region 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A6NGA9-F174.130.38

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 0 (showing top):

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

142 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM202FAM221BA6H8Z2646
TMEM202SPATA31D1Q6ZQQ2580
TMEM202OR4D10Q8NGI6553
TMEM202NT5C1BQ96P26516
TMEM202FNDC8Q8TC99480
TMEM202SPACA1Q9HBV2478
TMEM202CFAP45Q9UL16457
TMEM202CABYRO75952455
TMEM202SPEM3A0A1B0GUW6445
TMEM202SPATA18Q8TC71435
TMEM202SPATA31F1Q6ZU69415
TMEM202DNAH8Q96JB1409
TMEM202ADPGKQ9BRR6407
TMEM202PARP6Q2NL67402
TMEM202GARIN3Q8TC56386

IntAct

0 interactions, top by confidence:

BioGRID (1): TMEM202 (Positive Genetic)

ESM2 similar proteins: A2BGS3, A6NGA9, E7F594, O36364, O60478, O60883, O95800, O95838, P03208, P16849, P31389, P34590, P35367, P49219, Q03613, Q09351, Q09964, Q09965, Q14439, Q16950, Q16951, Q2KI97, Q3U3F9, Q5FVG1, Q5IXF8, Q5UAW9, Q60755, Q64017, Q66615, Q66H29, Q6P7G9, Q6SW98, Q6X632, Q7TSN5, Q7TSN6, Q80W35, Q80WT4, Q8BNQ3, Q8C206, Q8CIM5

Diamond homologs: A6NGA9, Q80W35

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance32
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

701 predictions. Top by Δscore:

VariantEffectΔscore
15:72406598:GCAG:Gacceptor_loss1.0000
15:72406599:CA:Cacceptor_loss1.0000
15:72406600:A:AGacceptor_gain1.0000
15:72406601:G:GGacceptor_gain1.0000
15:72406601:GATT:Gacceptor_gain1.0000
15:72405968:A:AGacceptor_gain0.9900
15:72405969:G:GGacceptor_gain0.9900
15:72406601:GAT:Gacceptor_gain0.9900
15:72406698:G:GTdonor_gain0.9900
15:72407077:T:TAacceptor_gain0.9900
15:72406596:AT:Aacceptor_gain0.9800
15:72406597:T:Gacceptor_gain0.9800
15:72406601:GA:Gacceptor_gain0.9800
15:72406601:GATTA:Gacceptor_gain0.9800
15:72407191:GC:Gdonor_gain0.9800
15:72407686:CGTA:Cacceptor_loss0.9800
15:72407687:GTA:Gacceptor_loss0.9800
15:72407688:TA:Tacceptor_loss0.9800
15:72407689:A:AGacceptor_gain0.9800
15:72407689:AG:Aacceptor_gain0.9800
15:72407689:AGG:Aacceptor_gain0.9800
15:72407690:G:GGacceptor_gain0.9800
15:72407690:GG:Gacceptor_gain0.9800
15:72407690:GGG:Gacceptor_gain0.9800
15:72406596:A:AGacceptor_gain0.9700
15:72406747:CTCAG:Cdonor_loss0.9700
15:72406748:TCAG:Tdonor_loss0.9700
15:72406750:AGG:Adonor_loss0.9700
15:72406751:GGTA:Gdonor_loss0.9700
15:72406752:GTACA:Gdonor_loss0.9700

AlphaMissense

1787 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
15:72398770:A:CS67R0.987
15:72398772:C:AS67R0.987
15:72398772:C:GS67R0.987
15:72398857:T:AW96R0.981
15:72398857:T:CW96R0.981
15:72398886:G:CW105C0.974
15:72398886:G:TW105C0.974
15:72407115:T:CF173L0.972
15:72407117:T:AF173L0.972
15:72407117:T:GF173L0.972
15:72398755:A:CS62R0.970
15:72398757:C:AS62R0.970
15:72398757:C:GS62R0.970
15:72398764:A:CS65R0.969
15:72398766:T:AS65R0.969
15:72398766:T:GS65R0.969
15:72398806:T:AW79R0.967
15:72398806:T:CW79R0.967
15:72406739:A:CS159R0.966
15:72406741:C:AS159R0.966
15:72406741:C:GS159R0.966
15:72407091:T:CC165R0.966
15:72407217:G:AG207R0.966
15:72407217:G:CG207R0.966
15:72407103:T:CC169R0.962
15:72398859:G:CW96C0.960
15:72398859:G:TW96C0.960
15:72407217:G:TG207W0.958
15:72398808:G:CW79C0.957
15:72398808:G:TW79C0.957

dbSNP variants (sampled 300 via entrez): RS1000487867 (15:72399018 C>T), RS1000801066 (15:72407209 T>A,C), RS1000884392 (15:72406865 A>C,G), RS1000955948 (15:72407523 T>C), RS1001084125 (15:72400566 A>C), RS1001105446 (15:72400439 A>G), RS1001313847 (15:72400203 G>T), RS1001832848 (15:72405014 A>G), RS1001928757 (15:72400088 A>G), RS1002212855 (15:72406057 G>C), RS1002242592 (15:72399166 T>C), RS1002432128 (15:72406484 C>G), RS1002573728 (15:72402437 C>T), RS1002671301 (15:72402730 A>G), RS1003088080 (15:72403271 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

3 total (human), top 3 by PubMed support.

ChemicalActions (top 5)PubMed papers
MT19c compounddecreases expression1
Air Pollutantsincreases expression1
Benzo(a)pyreneincreases methylation1

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.