TMEM213

gene
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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

FieldValue
HGNC IDHGNC:27220
Approved symbolTMEM213
Nametransmembrane protein 213
Location7q34
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000214128
Ensembl biotypeprotein_coding
Entrez155006

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

ExonStartEnd
ENSE00001529374138801327138801398
ENSE00001592437138802900138806759
ENSE00003844193138797994138798186

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 IDTPM avgSamples expressed
814190.198421

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
kidney epitheliumUBERON:000481999.24gold quality
renal medullaUBERON:000036297.98gold quality
adult mammalian kidneyUBERON:000008295.18gold quality
metanephros cortexUBERON:001053393.56gold quality
mucosa of paranasal sinusUBERON:000503093.40gold quality
buccal mucosa cellCL:000233693.24gold quality
parotid glandUBERON:000183193.13gold quality
kidneyUBERON:000211391.90gold quality
olfactory segment of nasal mucosaUBERON:000538687.30gold quality
cortex of kidneyUBERON:000122584.64gold quality
metanephrosUBERON:000008182.40gold quality
nasal cavity epitheliumUBERON:000538482.37silver quality
nasal cavity mucosaUBERON:000182679.22gold quality
endothelial cellCL:000011577.72silver quality
saliva-secreting glandUBERON:000104476.19gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047375.57gold quality
bronchial epithelial cellCL:000232874.82gold quality
bronchusUBERON:000218574.43gold quality
tracheaUBERON:000312672.54gold quality
adult organismUBERON:000702372.31gold quality
minor salivary glandUBERON:000183071.63gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099169.99gold quality
cardiac muscle of right atriumUBERON:000337969.84gold quality
left ventricle myocardiumUBERON:000656669.62gold quality
skin of legUBERON:000151169.57gold quality
upper arm skinUBERON:000426368.81gold quality
pancreatic ductal cellCL:000207968.65silver quality
zone of skinUBERON:000001467.92gold quality
mouth mucosaUBERON:000372967.79gold quality
skin of abdomenUBERON:000141666.03gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-CURD-135yes2151.49
E-GEOD-114530yes1691.70
E-CURD-119yes30.02
E-ANND-3yes6.19

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):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-5692A100.0074.406850
HSA-MIR-1213699.9872.815713
HSA-MIR-548N99.9871.944170
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-153-5P99.8973.866317
HSA-MIR-6783-3P99.8967.922059
HSA-MIR-4731-5P99.8967.232537
HSA-MIR-1343-3P99.8966.781815
HSA-MIR-4659A-3P99.8072.624248
HSA-MIR-4659B-3P99.8072.624248
HSA-MIR-204-5P99.7971.622439
HSA-MIR-211-5P99.7971.652440
HSA-MIR-323A-3P99.7970.301739
HSA-MIR-62399.7668.161170
HSA-MIR-3934-3P99.7665.511351
HSA-MIR-4766-5P99.7569.232662
HSA-MIR-4755-5P99.7170.342716
HSA-MIR-5006-3P99.7170.262728
HSA-MIR-120899.7068.281533
HSA-MIR-7-5P99.6770.531809
HSA-MIR-24-3P99.5969.971934
HSA-MIR-516B-5P99.5666.331495
HSA-MIR-6832-3P99.5270.441726
HSA-MIR-444199.4966.563216
HSA-MIR-4762-3P99.4369.722363
HSA-MIR-501-3P99.3366.12651
HSA-MIR-502-3P99.3366.12651
HSA-MIR-504-3P99.3067.181745
HSA-MIR-133A-3P99.2771.531270
HSA-MIR-133B99.2771.531270

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusTmem213ENSMUSG00000029829
rattus_norvegicusTmem213ENSRNOG00000085221

Protein

Protein identifiers

Transmembrane protein 213A2RRL7 (reviewed: A2RRL7)

All UniProt accessions (1): A2RRL7

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Endoplasmic reticulum membrane.

Isoforms (4)

UniProt IDNamesCanonical?
A2RRL7-11yes
A2RRL7-22
A2RRL7-33
A2RRL7-44

RefSeq proteins (1): NP_001078898* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR028121TMEM213Family

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)

ModelpLDDTFraction very-high
AF-A2RRL7-F169.090.19

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:

CategoryTerms
organelle membrane1
nuclear outer membrane-endoplasmic reticulum membrane network1
endoplasmic reticulum subcompartment1
cellular anatomical structure1

Protein interactions and networks

STRING

468 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM213TMEM207Q6UWW9596
TMEM213TMEM116Q8NCL8584
TMEM213TMEM25Q86YD3542
TMEM213RTP3Q9BQQ7528
TMEM213TMEM61Q8N0U2528
TMEM213NDC1Q9BTX1480
TMEM213C3orf22Q8N5N4479
TMEM213PLEKHG7Q6ZR37478
TMEM213TMEM72A0PK05447
TMEM213TMEM45AQ9NWC5447
TMEM213RNASE12Q5GAN4447
TMEM213C7orf33Q8WU49445
TMEM213C2orf15Q8WU43445
TMEM213SMIM17P0DL12434
TMEM213SLC35G2Q8TBE7434

IntAct

3 interactions, top by confidence:

ABTypeScore
TMEM213METAP2psi-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):

ClassificationCount (floor)
Pathogenic1
Likely pathogenic0
Uncertain significance14
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (1)

Variant IDHGVSClassification
149061GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1Pathogenic

SpliceAI

619 predictions. Top by Δscore:

VariantEffectΔscore
7:138801399:G:GGdonor_gain1.0000
7:138798183:GCAG:Gdonor_gain0.9900
7:138798187:GTAGC:Gdonor_loss0.9900
7:138798188:T:Gdonor_loss0.9900
7:138803044:A:Gdonor_gain0.9900
7:138803055:G:GTdonor_gain0.9900
7:138803064:GC:Gdonor_gain0.9900
7:138803128:G:Tdonor_gain0.9900
7:138837817:T:TAdonor_gain0.9900
7:138803066:G:GGdonor_gain0.9800
7:138803077:GC:Gdonor_gain0.9800
7:138803126:GGGGA:Gdonor_gain0.9800
7:138803127:GGGAG:Gdonor_gain0.9800
7:138803128:G:GTdonor_gain0.9800
7:138801325:A:AGacceptor_gain0.9700
7:138801326:G:GGacceptor_gain0.9700
7:138802898:A:AGacceptor_gain0.9700
7:138802899:G:GGacceptor_gain0.9700
7:138837846:T:Adonor_gain0.9700
7:138798193:T:Gdonor_gain0.9600
7:138800636:TTCTC:Tdonor_gain0.9600
7:138801326:GAA:Gacceptor_gain0.9600
7:138801487:TGTC:Tdonor_gain0.9600
7:138802899:GAC:Gacceptor_gain0.9600
7:138801326:GA:Gacceptor_gain0.9500
7:138837862:T:TAdonor_gain0.9500
7:138798184:C:Tdonor_gain0.9400
7:138798187:G:GGdonor_gain0.9400
7:138801393:GCCTC:Gdonor_gain0.9400
7:138798182:GGCAG:Gdonor_gain0.9300

AlphaMissense

691 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
7:138802983:A:CS80R0.996
7:138802985:C:AS80R0.996
7:138802985:C:GS80R0.996
7:138802980:T:AW79R0.995
7:138802980:T:CW79R0.995
7:138802961:G:CW72C0.991
7:138802961:G:TW72C0.991
7:138802959:T:AW72R0.988
7:138802959:T:CW72R0.988
7:138802992:T:CF83L0.985
7:138802994:C:AF83L0.985
7:138802994:C:GF83L0.985
7:138802978:G:AG78D0.984
7:138802977:G:CG78R0.982
7:138802972:C:AA76D0.979
7:138802975:T:AV77D0.978
7:138802989:T:AW82R0.977
7:138802989:T:CW82R0.977
7:138802993:T:CF83S0.970
7:138802971:G:CA76P0.969
7:138803013:T:CC90R0.969
7:138802982:G:CW79C0.968
7:138802982:G:TW79C0.968
7:138802929:T:CC62R0.966
7:138802911:T:CC56R0.963
7:138802956:G:TG71C0.963
7:138802932:T:CC63R0.961
7:138802911:T:AC56S0.960
7:138802912:G:CC56S0.960
7:138802969:C:AA75E0.960

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.

ChemicalActions (top 5)PubMed papers
Nickeldecreases expression2
aflatoxin B2decreases methylation1
Poly(amidoamine)decreases expression1
Zoledronic Aciddecreases expression1
Benzo(a)pyreneincreases methylation, decreases methylation1
Silicon Dioxidedecreases expression1
Tobacco Smoke Pollutionaffects 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.