TMEM202
gene geneOn 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
| Field | Value |
|---|---|
| HGNC ID | HGNC:33733 |
| Approved symbol | TMEM202 |
| Name | transmembrane protein 202 |
| Location | 15q23-q24.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | FLJ27523 |
| Ensembl gene | ENSG00000187806 |
| Ensembl biotype | protein_coding |
| Entrez | 338949 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00001366392 | 72398653 | 72398908 |
| ENSE00002577537 | 72398305 | 72398407 |
| ENSE00003463669 | 72406602 | 72406751 |
| ENSE00003521149 | 72407691 | 72408367 |
| ENSE00003660338 | 72407086 | 72407217 |
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 ID | TPM avg | Samples expressed |
|---|---|---|
| 147577 | 0.0236 | 3 |
Top tissues by expression
107 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 94.76 | gold quality |
| left testis | UBERON:0004533 | 85.94 | gold quality |
| testis | UBERON:0000473 | 85.41 | gold quality |
| right testis | UBERON:0004534 | 84.32 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 78.55 | gold quality |
| quadriceps femoris | UBERON:0001377 | 77.26 | gold quality |
| thymus | UBERON:0002370 | 56.63 | silver quality |
| hindlimb stylopod muscle | UBERON:0004252 | 40.84 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| sural nerve | UBERON:0015488 | 36.26 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 33.70 | gold quality |
| monocyte | CL:0000576 | 32.22 | gold quality |
| bone marrow | UBERON:0002371 | 32.02 | gold quality |
| leukocyte | CL:0000738 | 31.80 | gold quality |
| muscle tissue | UBERON:0002385 | 31.31 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| prefrontal cortex | UBERON:0000451 | 29.85 | gold quality |
| liver | UBERON:0002107 | 29.37 | gold quality |
| ectocervix | UBERON:0012249 | 28.45 | silver quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| placenta | UBERON:0001987 | 28.05 | silver quality |
| superior frontal gyrus | UBERON:0002661 | 27.69 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| blood | UBERON:0000178 | 27.52 | silver quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.94 |
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):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-499A-5P | 99.98 | 70.79 | 1323 |
| HSA-MIR-7152-3P | 99.97 | 67.47 | 849 |
| HSA-MIR-3658 | 99.96 | 73.87 | 4379 |
| HSA-MIR-5680 | 99.91 | 69.83 | 3421 |
| HSA-MIR-1297 | 99.91 | 73.41 | 3162 |
| HSA-MIR-8076 | 99.78 | 68.52 | 1170 |
| HSA-MIR-3617-5P | 99.75 | 69.41 | 1968 |
| HSA-MIR-641 | 99.75 | 69.35 | 1975 |
| HSA-MIR-4699-3P | 99.71 | 70.15 | 3142 |
| HSA-MIR-7159-5P | 99.53 | 72.12 | 2472 |
| HSA-MIR-155-5P | 99.35 | 70.16 | 1509 |
| HSA-MIR-4279 | 99.19 | 66.70 | 2437 |
| HSA-MIR-5583-3P | 99.06 | 65.68 | 1018 |
| HSA-MIR-10B-3P | 99.04 | 66.98 | 988 |
| HSA-MIR-421 | 98.90 | 67.04 | 1883 |
| HSA-MIR-3145-3P | 98.85 | 69.07 | 2031 |
| HSA-MIR-7977 | 98.65 | 66.18 | 2590 |
| HSA-MIR-4709-5P | 98.51 | 67.25 | 1335 |
| HSA-MIR-4490 | 98.51 | 68.47 | 943 |
| HSA-MIR-6801-3P | 98.04 | 64.64 | 805 |
| HSA-MIR-6810-3P | 97.96 | 64.57 | 1023 |
| HSA-MIR-5000-5P | 97.40 | 66.11 | 1055 |
| HSA-MIR-3663-5P | 97.01 | 64.84 | 713 |
| HSA-MIR-10525-3P | 96.32 | 68.04 | 699 |
| HSA-MIR-208A-3P | 95.87 | 66.51 | 397 |
| HSA-MIR-208B-3P | 95.87 | 66.56 | 396 |
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 202 — A6NGA9 (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)
| ID | Name | Type |
|---|---|---|
| IPR050579 | PMP-22/EMP/MP20-like | Family |
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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A6NGA9-F1 | 74.13 | 0.38 |
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:
| Category | Terms |
|---|---|
| membrane | 1 |
| cell periphery | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
142 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| TMEM202 | FAM221B | A6H8Z2 | 646 |
| TMEM202 | SPATA31D1 | Q6ZQQ2 | 580 |
| TMEM202 | OR4D10 | Q8NGI6 | 553 |
| TMEM202 | NT5C1B | Q96P26 | 516 |
| TMEM202 | FNDC8 | Q8TC99 | 480 |
| TMEM202 | SPACA1 | Q9HBV2 | 478 |
| TMEM202 | CFAP45 | Q9UL16 | 457 |
| TMEM202 | CABYR | O75952 | 455 |
| TMEM202 | SPEM3 | A0A1B0GUW6 | 445 |
| TMEM202 | SPATA18 | Q8TC71 | 435 |
| TMEM202 | SPATA31F1 | Q6ZU69 | 415 |
| TMEM202 | DNAH8 | Q96JB1 | 409 |
| TMEM202 | ADPGK | Q9BRR6 | 407 |
| TMEM202 | PARP6 | Q2NL67 | 402 |
| TMEM202 | GARIN3 | Q8TC56 | 386 |
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):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 32 |
| Likely benign | 3 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
701 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 15:72406598:GCAG:G | acceptor_loss | 1.0000 |
| 15:72406599:CA:C | acceptor_loss | 1.0000 |
| 15:72406600:A:AG | acceptor_gain | 1.0000 |
| 15:72406601:G:GG | acceptor_gain | 1.0000 |
| 15:72406601:GATT:G | acceptor_gain | 1.0000 |
| 15:72405968:A:AG | acceptor_gain | 0.9900 |
| 15:72405969:G:GG | acceptor_gain | 0.9900 |
| 15:72406601:GAT:G | acceptor_gain | 0.9900 |
| 15:72406698:G:GT | donor_gain | 0.9900 |
| 15:72407077:T:TA | acceptor_gain | 0.9900 |
| 15:72406596:AT:A | acceptor_gain | 0.9800 |
| 15:72406597:T:G | acceptor_gain | 0.9800 |
| 15:72406601:GA:G | acceptor_gain | 0.9800 |
| 15:72406601:GATTA:G | acceptor_gain | 0.9800 |
| 15:72407191:GC:G | donor_gain | 0.9800 |
| 15:72407686:CGTA:C | acceptor_loss | 0.9800 |
| 15:72407687:GTA:G | acceptor_loss | 0.9800 |
| 15:72407688:TA:T | acceptor_loss | 0.9800 |
| 15:72407689:A:AG | acceptor_gain | 0.9800 |
| 15:72407689:AG:A | acceptor_gain | 0.9800 |
| 15:72407689:AGG:A | acceptor_gain | 0.9800 |
| 15:72407690:G:GG | acceptor_gain | 0.9800 |
| 15:72407690:GG:G | acceptor_gain | 0.9800 |
| 15:72407690:GGG:G | acceptor_gain | 0.9800 |
| 15:72406596:A:AG | acceptor_gain | 0.9700 |
| 15:72406747:CTCAG:C | donor_loss | 0.9700 |
| 15:72406748:TCAG:T | donor_loss | 0.9700 |
| 15:72406750:AGG:A | donor_loss | 0.9700 |
| 15:72406751:GGTA:G | donor_loss | 0.9700 |
| 15:72406752:GTACA:G | donor_loss | 0.9700 |
AlphaMissense
1787 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 15:72398770:A:C | S67R | 0.987 |
| 15:72398772:C:A | S67R | 0.987 |
| 15:72398772:C:G | S67R | 0.987 |
| 15:72398857:T:A | W96R | 0.981 |
| 15:72398857:T:C | W96R | 0.981 |
| 15:72398886:G:C | W105C | 0.974 |
| 15:72398886:G:T | W105C | 0.974 |
| 15:72407115:T:C | F173L | 0.972 |
| 15:72407117:T:A | F173L | 0.972 |
| 15:72407117:T:G | F173L | 0.972 |
| 15:72398755:A:C | S62R | 0.970 |
| 15:72398757:C:A | S62R | 0.970 |
| 15:72398757:C:G | S62R | 0.970 |
| 15:72398764:A:C | S65R | 0.969 |
| 15:72398766:T:A | S65R | 0.969 |
| 15:72398766:T:G | S65R | 0.969 |
| 15:72398806:T:A | W79R | 0.967 |
| 15:72398806:T:C | W79R | 0.967 |
| 15:72406739:A:C | S159R | 0.966 |
| 15:72406741:C:A | S159R | 0.966 |
| 15:72406741:C:G | S159R | 0.966 |
| 15:72407091:T:C | C165R | 0.966 |
| 15:72407217:G:A | G207R | 0.966 |
| 15:72407217:G:C | G207R | 0.966 |
| 15:72407103:T:C | C169R | 0.962 |
| 15:72398859:G:C | W96C | 0.960 |
| 15:72398859:G:T | W96C | 0.960 |
| 15:72407217:G:T | G207W | 0.958 |
| 15:72398808:G:C | W79C | 0.957 |
| 15:72398808:G:T | W79C | 0.957 |
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.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| MT19c compound | decreases expression | 1 |
| Air Pollutants | increases expression | 1 |
| Benzo(a)pyrene | increases methylation | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.