TMEM213
gene geneOn this page
Summary
TMEM213 (transmembrane protein 213, HGNC:27220) is a protein-coding gene on chromosome 7q34, encoding Transmembrane protein 213 (A2RRL7).
Predicted to be located in membrane.
Source: NCBI Gene 155006 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 17 total — 1 pathogenic
- MANE Select transcript:
NM_001085429
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:27220 |
| Approved symbol | TMEM213 |
| Name | transmembrane protein 213 |
| Location | 7q34 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000214128 |
| Ensembl biotype | protein_coding |
| Entrez | 155006 |
Gene structure
Transcript identifiers
Ensembl transcripts: 6 — 5 protein_coding, 1 retained_intron
ENST00000397602, ENST00000413208, ENST00000442682, ENST00000458494, ENST00000472775, ENST00000869134
RefSeq mRNA: 1 — MANE Select: NM_001085429
NM_001085429
CCDS: CCDS47722
Canonical transcript exons
ENST00000442682 — 3 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001529374 | 138801327 | 138801398 |
| ENSE00001592437 | 138802900 | 138806759 |
| ENSE00003844193 | 138797994 | 138798186 |
Expression profiles
Bgee: expression breadth ubiquitous, 107 present calls, max score 99.24.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.1984 / max 69.1880, expressed in 21 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 81419 | 0.1984 | 21 |
Top tissues by expression
209 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| kidney epithelium | UBERON:0004819 | 99.24 | gold quality |
| renal medulla | UBERON:0000362 | 97.98 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 95.18 | gold quality |
| metanephros cortex | UBERON:0010533 | 93.56 | gold quality |
| mucosa of paranasal sinus | UBERON:0005030 | 93.40 | gold quality |
| buccal mucosa cell | CL:0002336 | 93.24 | gold quality |
| parotid gland | UBERON:0001831 | 93.13 | gold quality |
| kidney | UBERON:0002113 | 91.90 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 87.30 | gold quality |
| cortex of kidney | UBERON:0001225 | 84.64 | gold quality |
| metanephros | UBERON:0000081 | 82.40 | gold quality |
| nasal cavity epithelium | UBERON:0005384 | 82.37 | silver quality |
| nasal cavity mucosa | UBERON:0001826 | 79.22 | gold quality |
| endothelial cell | CL:0000115 | 77.72 | silver quality |
| saliva-secreting gland | UBERON:0001044 | 76.19 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 75.57 | gold quality |
| bronchial epithelial cell | CL:0002328 | 74.82 | gold quality |
| bronchus | UBERON:0002185 | 74.43 | gold quality |
| trachea | UBERON:0003126 | 72.54 | gold quality |
| adult organism | UBERON:0007023 | 72.31 | gold quality |
| minor salivary gland | UBERON:0001830 | 71.63 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 69.99 | gold quality |
| cardiac muscle of right atrium | UBERON:0003379 | 69.84 | gold quality |
| left ventricle myocardium | UBERON:0006566 | 69.62 | gold quality |
| skin of leg | UBERON:0001511 | 69.57 | gold quality |
| upper arm skin | UBERON:0004263 | 68.81 | gold quality |
| pancreatic ductal cell | CL:0002079 | 68.65 | silver quality |
| zone of skin | UBERON:0000014 | 67.92 | gold quality |
| mouth mucosa | UBERON:0003729 | 67.79 | gold quality |
| skin of abdomen | UBERON:0001416 | 66.03 | gold quality |
Single-cell (SCXA)
Detected in 4 experiment(s), a significant marker in 4.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-CURD-135 | yes | 2151.49 |
| E-GEOD-114530 | yes | 1691.70 |
| E-CURD-119 | yes | 30.02 |
| E-ANND-3 | yes | 6.19 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
57 targeting TMEM213, 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-5692A | 100.00 | 74.40 | 6850 |
| HSA-MIR-12136 | 99.98 | 72.81 | 5713 |
| HSA-MIR-548N | 99.98 | 71.94 | 4170 |
| HSA-MIR-6778-3P | 99.96 | 67.29 | 2693 |
| HSA-MIR-153-5P | 99.89 | 73.86 | 6317 |
| HSA-MIR-6783-3P | 99.89 | 67.92 | 2059 |
| HSA-MIR-4731-5P | 99.89 | 67.23 | 2537 |
| HSA-MIR-1343-3P | 99.89 | 66.78 | 1815 |
| HSA-MIR-4659A-3P | 99.80 | 72.62 | 4248 |
| HSA-MIR-4659B-3P | 99.80 | 72.62 | 4248 |
| HSA-MIR-204-5P | 99.79 | 71.62 | 2439 |
| HSA-MIR-211-5P | 99.79 | 71.65 | 2440 |
| HSA-MIR-323A-3P | 99.79 | 70.30 | 1739 |
| HSA-MIR-623 | 99.76 | 68.16 | 1170 |
| HSA-MIR-3934-3P | 99.76 | 65.51 | 1351 |
| HSA-MIR-4766-5P | 99.75 | 69.23 | 2662 |
| HSA-MIR-4755-5P | 99.71 | 70.34 | 2716 |
| HSA-MIR-5006-3P | 99.71 | 70.26 | 2728 |
| HSA-MIR-1208 | 99.70 | 68.28 | 1533 |
| HSA-MIR-7-5P | 99.67 | 70.53 | 1809 |
| HSA-MIR-24-3P | 99.59 | 69.97 | 1934 |
| HSA-MIR-516B-5P | 99.56 | 66.33 | 1495 |
| HSA-MIR-6832-3P | 99.52 | 70.44 | 1726 |
| HSA-MIR-4441 | 99.49 | 66.56 | 3216 |
| HSA-MIR-4762-3P | 99.43 | 69.72 | 2363 |
| HSA-MIR-501-3P | 99.33 | 66.12 | 651 |
| HSA-MIR-502-3P | 99.33 | 66.12 | 651 |
| HSA-MIR-504-3P | 99.30 | 67.18 | 1745 |
| HSA-MIR-133A-3P | 99.27 | 71.53 | 1270 |
| HSA-MIR-133B | 99.27 | 71.53 | 1270 |
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Tmem213 | ENSMUSG00000029829 |
| rattus_norvegicus | Tmem213 | ENSRNOG00000085221 |
Protein
Protein identifiers
Transmembrane protein 213 — A2RRL7 (reviewed: A2RRL7)
All UniProt accessions (1): A2RRL7
UniProt curated annotations — full annotation on UniProt →
Subcellular location. Endoplasmic reticulum membrane.
Isoforms (4)
| UniProt ID | Names | Canonical? |
|---|---|---|
| A2RRL7-1 | 1 | yes |
| A2RRL7-2 | 2 | |
| A2RRL7-3 | 3 | |
| A2RRL7-4 | 4 |
RefSeq proteins (1): NP_001078898* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR028121 | TMEM213 | Family |
Pfam: PF15192
UniProt features (8 total): splice variant 3, topological domain 2, signal peptide 1, chain 1, transmembrane region 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A2RRL7-F1 | 69.09 | 0.19 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 42 (showing top):
SCHAEFFER_PROSTATE_DEVELOPMENT_48HR_DN, GOCC_NUCLEAR_OUTER_MEMBRANE_ENDOPLASMIC_RETICULUM_MEMBRANE_NETWORK, GOCC_ORGANELLE_SUBCOMPARTMENT, DODD_NASOPHARYNGEAL_CARCINOMA_DN, MARTENS_TRETINOIN_RESPONSE_UP, LEE_BMP2_TARGETS_UP, GLI4_TARGET_GENES, NFKBIA_TARGET_GENES, GSE10239_MEMORY_VS_KLRG1INT_EFF_CD8_TCELL_UP, GSE10239_MEMORY_VS_KLRG1HIGH_EFF_CD8_TCELL_UP, MIR4755_5P, MIR5006_3P, MIR204_5P, MIR211_5P, GSE10239_MEMORY_VS_DAY4.5_EFF_CD8_TCELL_UP
GO Biological Process (0):
GO Molecular Function (0):
GO Cellular Component (2): endoplasmic reticulum membrane (GO:0005789), membrane (GO:0016020)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| organelle membrane | 1 |
| nuclear outer membrane-endoplasmic reticulum membrane network | 1 |
| endoplasmic reticulum subcompartment | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
468 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| TMEM213 | TMEM207 | Q6UWW9 | 596 |
| TMEM213 | TMEM116 | Q8NCL8 | 584 |
| TMEM213 | TMEM25 | Q86YD3 | 542 |
| TMEM213 | RTP3 | Q9BQQ7 | 528 |
| TMEM213 | TMEM61 | Q8N0U2 | 528 |
| TMEM213 | NDC1 | Q9BTX1 | 480 |
| TMEM213 | C3orf22 | Q8N5N4 | 479 |
| TMEM213 | PLEKHG7 | Q6ZR37 | 478 |
| TMEM213 | TMEM72 | A0PK05 | 447 |
| TMEM213 | TMEM45A | Q9NWC5 | 447 |
| TMEM213 | RNASE12 | Q5GAN4 | 447 |
| TMEM213 | C7orf33 | Q8WU49 | 445 |
| TMEM213 | C2orf15 | Q8WU43 | 445 |
| TMEM213 | SMIM17 | P0DL12 | 434 |
| TMEM213 | SLC35G2 | Q8TBE7 | 434 |
IntAct
3 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| TMEM213 | METAP2 | psi-mi:“MI:0914”(association) | 0.530 |
BioGRID (13): TMEM213 (Two-hybrid), TMEM213 (Two-hybrid), METAP2 (Affinity Capture-MS), DCUN1D5 (Affinity Capture-MS), GLMN (Affinity Capture-MS), EFNB1 (Affinity Capture-MS), ALG11 (Affinity Capture-MS), TMEM213 (Two-hybrid), TMEM213 (Two-hybrid), EFNB1 (Affinity Capture-MS), METAP2 (Affinity Capture-MS), ALG11 (Affinity Capture-MS), GLMN (Affinity Capture-MS)
ESM2 similar proteins: A0A1B0GST9, A0A1B0GTU2, A0A1B0GV90, A0A590UK83, A2RRL7, A7S641, A8WG88, A9JTJ0, B9X187, K7EJ46, O00168, O08589, O13001, P0C2S0, P15383, P41237, P56513, P60606, P63160, P63161, Q04645, Q04646, Q04679, Q04680, Q0P467, Q28EH9, Q3SZX0, Q3UJ81, Q3URE8, Q3ZBP2, Q4LDR2, Q4R6L9, Q502I1, Q592E4, Q5XF36, Q6AXF6, Q6NWH5, Q6PBK8, Q6Q3F5, Q71RC9
Diamond homologs: A2RRL7, Q08EA8, Q58CU5
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
17 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 1 |
| Likely pathogenic | 0 |
| Uncertain significance | 14 |
| Likely benign | 2 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (1)
| Variant ID | HGVS | Classification |
|---|---|---|
| 149061 | GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 | Pathogenic |
SpliceAI
619 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 7:138801399:G:GG | donor_gain | 1.0000 |
| 7:138798183:GCAG:G | donor_gain | 0.9900 |
| 7:138798187:GTAGC:G | donor_loss | 0.9900 |
| 7:138798188:T:G | donor_loss | 0.9900 |
| 7:138803044:A:G | donor_gain | 0.9900 |
| 7:138803055:G:GT | donor_gain | 0.9900 |
| 7:138803064:GC:G | donor_gain | 0.9900 |
| 7:138803128:G:T | donor_gain | 0.9900 |
| 7:138837817:T:TA | donor_gain | 0.9900 |
| 7:138803066:G:GG | donor_gain | 0.9800 |
| 7:138803077:GC:G | donor_gain | 0.9800 |
| 7:138803126:GGGGA:G | donor_gain | 0.9800 |
| 7:138803127:GGGAG:G | donor_gain | 0.9800 |
| 7:138803128:G:GT | donor_gain | 0.9800 |
| 7:138801325:A:AG | acceptor_gain | 0.9700 |
| 7:138801326:G:GG | acceptor_gain | 0.9700 |
| 7:138802898:A:AG | acceptor_gain | 0.9700 |
| 7:138802899:G:GG | acceptor_gain | 0.9700 |
| 7:138837846:T:A | donor_gain | 0.9700 |
| 7:138798193:T:G | donor_gain | 0.9600 |
| 7:138800636:TTCTC:T | donor_gain | 0.9600 |
| 7:138801326:GAA:G | acceptor_gain | 0.9600 |
| 7:138801487:TGTC:T | donor_gain | 0.9600 |
| 7:138802899:GAC:G | acceptor_gain | 0.9600 |
| 7:138801326:GA:G | acceptor_gain | 0.9500 |
| 7:138837862:T:TA | donor_gain | 0.9500 |
| 7:138798184:C:T | donor_gain | 0.9400 |
| 7:138798187:G:GG | donor_gain | 0.9400 |
| 7:138801393:GCCTC:G | donor_gain | 0.9400 |
| 7:138798182:GGCAG:G | donor_gain | 0.9300 |
AlphaMissense
691 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 7:138802983:A:C | S80R | 0.996 |
| 7:138802985:C:A | S80R | 0.996 |
| 7:138802985:C:G | S80R | 0.996 |
| 7:138802980:T:A | W79R | 0.995 |
| 7:138802980:T:C | W79R | 0.995 |
| 7:138802961:G:C | W72C | 0.991 |
| 7:138802961:G:T | W72C | 0.991 |
| 7:138802959:T:A | W72R | 0.988 |
| 7:138802959:T:C | W72R | 0.988 |
| 7:138802992:T:C | F83L | 0.985 |
| 7:138802994:C:A | F83L | 0.985 |
| 7:138802994:C:G | F83L | 0.985 |
| 7:138802978:G:A | G78D | 0.984 |
| 7:138802977:G:C | G78R | 0.982 |
| 7:138802972:C:A | A76D | 0.979 |
| 7:138802975:T:A | V77D | 0.978 |
| 7:138802989:T:A | W82R | 0.977 |
| 7:138802989:T:C | W82R | 0.977 |
| 7:138802993:T:C | F83S | 0.970 |
| 7:138802971:G:C | A76P | 0.969 |
| 7:138803013:T:C | C90R | 0.969 |
| 7:138802982:G:C | W79C | 0.968 |
| 7:138802982:G:T | W79C | 0.968 |
| 7:138802929:T:C | C62R | 0.966 |
| 7:138802911:T:C | C56R | 0.963 |
| 7:138802956:G:T | G71C | 0.963 |
| 7:138802932:T:C | C63R | 0.961 |
| 7:138802911:T:A | C56S | 0.960 |
| 7:138802912:G:C | C56S | 0.960 |
| 7:138802969:C:A | A75E | 0.960 |
dbSNP variants (sampled 300 via entrez): RS1000067797 (7:138801313 A>G), RS1000205377 (7:138797011 C>T), RS1000351177 (7:138796459 T>C), RS1000911349 (7:138806239 G>C), RS1001070308 (7:138799689 T>C), RS1001313258 (7:138800441 T>C), RS1001773673 (7:138797066 G>A,T), RS1001923626 (7:138802266 T>C,G), RS1002292636 (7:138802493 G>A), RS1002306485 (7:138799103 T>C), RS1002683593 (7:138799322 G>A), RS1002896846 (7:138805252 A>C), RS1003297120 (7:138804167 C>T), RS1003332623 (7:138803526 C>T), RS1003413302 (7:138803893 G>C)
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
7 total (human), top 7 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Nickel | decreases expression | 2 |
| aflatoxin B2 | decreases methylation | 1 |
| Poly(amidoamine) | decreases expression | 1 |
| Zoledronic Acid | decreases expression | 1 |
| Benzo(a)pyrene | increases methylation, decreases methylation | 1 |
| Silicon Dioxide | decreases expression | 1 |
| Tobacco Smoke Pollution | affects expression | 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.