TMEM225B

gene
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Summary

TMEM225B (transmembrane protein 225B, HGNC:53075) is a protein-coding gene on chromosome 7q22.1, encoding Transmembrane protein 225B (P0DP42).

Predicted to be located in membrane.

Source: NCBI Gene 100289187 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 1 total
  • MANE Select transcript: NM_001195541

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:53075
Approved symbolTMEM225B
Nametransmembrane protein 225B
Location7q22.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000244219
Ensembl biotypeprotein_coding
Entrez100289187

Gene structure

Transcript identifiers

Ensembl transcripts: 9 — 8 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000429679, ENST00000431679, ENST00000453227, ENST00000877211, ENST00000877212, ENST00000877213, ENST00000877214, ENST00000877215, ENST00000961685

RefSeq mRNA: 3 — MANE Select: NM_001195541 NM_001195541, NM_001195542, NM_001195543

CCDS: CCDS87525

Canonical transcript exons

ENST00000431679 — 6 exons

ExonStartEnd
ENSE000017436279959826799598381
ENSE000017544149961039399611045
ENSE000035094619960767399607810
ENSE000035215279960020599600285
ENSE000036218309960674899606894
ENSE000038073859960438699604596

Expression profiles

Bgee: expression breadth ubiquitous, 164 present calls, max score 98.01.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.3419 / max 283.7325, expressed in 7 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
798930.27556
798940.04394
798910.01163
798920.01103

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
left testisUBERON:000453398.01gold quality
adult organismUBERON:000702397.75gold quality
right testisUBERON:000453497.68gold quality
spermCL:000001995.94gold quality
testisUBERON:000047395.89gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099194.38gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047389.51gold quality
amniotic fluidUBERON:000017376.79gold quality
mucosa of stomachUBERON:000119973.38gold quality
skin of legUBERON:000151173.02gold quality
upper arm skinUBERON:000426372.75gold quality
stromal cell of endometriumCL:000225571.81gold quality
tibial nerveUBERON:000132371.08gold quality
subcutaneous adipose tissueUBERON:000219071.06gold quality
endothelial cellCL:000011571.05gold quality
zone of skinUBERON:000001470.67gold quality
skin of abdomenUBERON:000141670.29gold quality
lower esophagus mucosaUBERON:003583469.93gold quality
islet of LangerhansUBERON:000000669.43gold quality
metanephros cortexUBERON:001053368.82gold quality
adipose tissueUBERON:000101368.79gold quality
right adrenal gland cortexUBERON:003582768.19gold quality
C1 segment of cervical spinal cordUBERON:000646968.13gold quality
adenohypophysisUBERON:000219667.81gold quality
left lobe of thyroid glandUBERON:000112067.75gold quality
left uterine tubeUBERON:000130367.56gold quality
left adrenal glandUBERON:000123467.50gold quality
amygdalaUBERON:000187667.46gold quality
pituitary glandUBERON:000000767.38gold quality
ectocervixUBERON:001224967.36gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.18

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

23 targeting TMEM225B, 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-318599.9968.121959
HSA-MIR-6825-5P99.9669.813431
HSA-MIR-6744-5P99.9366.82748
HSA-MIR-3150A-3P99.7664.441640
HSA-MIR-6763-5P99.7664.681767
HSA-MIR-613499.6365.681537
HSA-MIR-488-3P99.6168.791731
HSA-MIR-451B99.5568.281380
HSA-MIR-569099.2567.581012
HSA-MIR-4717-3P99.0666.341072
HSA-MIR-6868-5P99.0665.691284
HSA-MIR-315498.9466.551455
HSA-MIR-219A-1-3P98.9167.87639
HSA-MIR-129-1-3P98.8668.41779
HSA-MIR-129-2-3P98.8668.41779
HSA-MIR-463598.7467.631339
HSA-MIR-3928-5P98.5067.48980
HSA-MIR-6806-3P98.5067.31980
HSA-MIR-939-5P97.1065.801579
HSA-MIR-6730-3P97.0367.54889
HSA-MIR-6854-5P96.7765.96848
HSA-MIR-1343-5P96.4866.061506
HSA-MIR-426894.4564.09819

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Transmembrane protein 225BP0DP42 (reviewed: P0DP42)

All UniProt accessions (1): P0DP42

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

RefSeq proteins (3): NP_001182470, NP_001182471, NP_001182472 (=MANE)

Domains & families (InterPro)

IDNameType
IPR033542TM225Family
IPR057351TM225_domDomain

Pfam: PF25452

UniProt features (5 total): transmembrane region 4, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P0DP42-F177.060.37

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 11 (showing top): SENGUPTA_EBNA1_ANTICORRELATED, GRABARCZYK_BCL11B_TARGETS_DN, FOXN3_TARGET_GENES, HMGA1_TARGET_GENES, MIR6825_5P, MIR6854_5P, chr7q22, ZNF320_TARGET_GENES, GSE2770_TGFB_AND_IL4_VS_IL12_TREATED_ACT_CD4_TCELL_2H_DN, GSE34156_UNTREATED_VS_6H_NOD2_AND_TLR1_TLR2_LIGAND_TREATED_MONOCYTE_UP, GSE34156_NOD2_LIGAND_VS_NOD2_AND_TLR1_TLR2_LIGAND_24H_TREATED_MONOCYTE_UP

GO Biological Process (1): negative regulation of phosphatase activity (GO:0010923)

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
regulation of phosphatase activity1
phosphatase activity1
negative regulation of dephosphorylation1
negative regulation of hydrolase activity1
binding1
cellular anatomical structure1

Protein interactions and networks

STRING

174 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM225BTMEM225Q6GV28654
TMEM225BKBTBD3Q8NAB2593
TMEM225BTMEM255BQ8WV15506
TMEM225BTMEM151AQ8N4L1474
TMEM225BFSCN3Q9NQT6460
TMEM225BTBC1D10BQ4KMP7409
TMEM225BTMEM65Q6PI78408
TMEM225BPRM3Q9NNZ6407
TMEM225BTUBGCP4Q9UGJ1401
TMEM225BZNF695Q8IW36392
TMEM225BEXD2Q9NVH0371
TMEM225BYIPF7Q8N8F6370
TMEM225BTFIP11Q9UBB9356
TMEM225BIFT22Q9H7X7351
TMEM225BCCDC187A0A096LP49347

IntAct

127 interactions, top by confidence:

ABTypeScore
YIF1ATMEM225Bpsi-mi:“MI:0915”(physical association)0.560
SNX27TMEM225Bpsi-mi:“MI:0407”(direct interaction)0.440
TMEM225BPDZD7psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BMAST2psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BSNTB1psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BPDZK1psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BSNTA1psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BWHRNpsi-mi:“MI:0407”(direct interaction)0.440
TMEM225BPTPN3psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BLNX2psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BRHPN1psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BDLG3psi-mi:“MI:0407”(direct interaction)0.440
DLG1TMEM225Bpsi-mi:“MI:0407”(direct interaction)0.440
TMEM225BPARD3psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BSCRIBpsi-mi:“MI:0407”(direct interaction)0.440
TMEM225BHTRA1psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BMAST1psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BPATJpsi-mi:“MI:0407”(direct interaction)0.440
TMEM225BPARD3Bpsi-mi:“MI:0407”(direct interaction)0.440
TMEM225BSNTG2psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BLIN7Cpsi-mi:“MI:0407”(direct interaction)0.440
TMEM225BDLG2psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BDLG4psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BPICK1psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BSYNJ2BPpsi-mi:“MI:0407”(direct interaction)0.440
TMEM225BPDZD2psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BDLG1psi-mi:“MI:0407”(direct interaction)0.440
TMEM225BAPBA3psi-mi:“MI:0407”(direct interaction)0.440

ESM2 similar proteins: A0A494BZU4, A0A7H0DND7, A0JNG0, A2T345, A4IIV4, C4QM85, E7F594, G5EDX4, O02051, O45306, P0DP42, P0DST5, P0DST6, P21061, P24763, P34362, P34363, P53053, Q09282, Q0II41, Q10907, Q11071, Q11085, Q13571, Q20249, Q297K8, Q2KHT4, Q2KJA5, Q32KQ5, Q5DC12, Q5GH77, Q5PQM0, Q5RD28, Q5REZ0, Q5TAH2, Q61168, Q6AXT9, Q6GV27, Q6GV28, Q7K1V5

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 78 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

Reactome pathways:

PathwayPartnersFoldFDR
Ras activation upon Ca2+ influx through NMDA receptor556.0×1e-06
Unblocking of NMDA receptors, glutamate binding and activation553.3×1e-06
Negative regulation of NMDA receptor-mediated neuronal transmission553.3×1e-06
Assembly and cell surface presentation of NMDA receptors1049.8×4e-13
Dopamine Neurotransmitter Release Cycle548.7×1e-06
Long-term potentiation546.6×1e-06
Neurexins and neuroligins1142.5×2e-13
Protein-protein interactions at synapses736.5×5e-08

GO biological processes:

GO termPartnersFoldFDR
establishment or maintenance of epithelial cell apical/basal polarity1185.2×1e-16
protein localization to synapse661.3×5e-08
receptor clustering758.2×5e-09
regulation of postsynaptic membrane neurotransmitter receptor levels746.3×2e-08
protein-containing complex assembly913.7×1e-06
cell-cell adhesion1013.5×2e-07
protein localization to plasma membrane57.2×8e-03
chemical synaptic transmission77.2×1e-03

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance1
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

951 predictions. Top by Δscore:

VariantEffectΔscore
7:99600286:G:GGdonor_gain1.0000
7:99604577:G:GTdonor_gain1.0000
7:99604597:G:GGdonor_gain1.0000
7:99606746:A:AGacceptor_gain1.0000
7:99606747:G:GGacceptor_gain1.0000
7:99606854:G:GTdonor_gain1.0000
7:99606906:C:Gdonor_gain1.0000
7:99598389:G:Tdonor_gain0.9900
7:99600204:GCA:Gacceptor_gain0.9900
7:99600281:GACCT:Gdonor_gain0.9900
7:99604382:A:AGacceptor_gain0.9900
7:99604382:ACAG:Aacceptor_gain0.9900
7:99604383:C:Gacceptor_gain0.9900
7:99604383:CA:Cacceptor_loss0.9900
7:99604384:A:ATacceptor_loss0.9900
7:99604384:AGGT:Aacceptor_gain0.9900
7:99604385:GGT:Gacceptor_gain0.9900
7:99604385:GGTG:Gacceptor_gain0.9900
7:99604527:G:GTdonor_gain0.9900
7:99604592:ATCCA:Adonor_gain0.9900
7:99604593:TCCA:Tdonor_gain0.9900
7:99604594:CCA:Cdonor_gain0.9900
7:99604595:CAGTA:Cdonor_loss0.9900
7:99604596:AG:Adonor_loss0.9900
7:99604597:GT:Gdonor_loss0.9900
7:99604598:TAA:Tdonor_loss0.9900
7:99604602:G:GTdonor_gain0.9900
7:99604606:G:Tdonor_gain0.9900
7:99606747:GT:Gacceptor_gain0.9900
7:99606747:GTTT:Gacceptor_gain0.9900

AlphaMissense

1446 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
7:99606882:A:CS115R0.984
7:99606884:C:AS115R0.984
7:99606884:C:GS115R0.984
7:99604499:G:CW37C0.982
7:99604499:G:TW37C0.982
7:99604497:T:AW37R0.980
7:99604497:T:CW37R0.980
7:99606762:G:CG75R0.980
7:99604548:T:CF54L0.979
7:99604550:T:AF54L0.979
7:99604550:T:GF54L0.979
7:99604458:G:CG24R0.970
7:99604549:T:GF54C0.969
7:99607798:T:CF161L0.968
7:99607800:C:AF161L0.968
7:99607800:C:GF161L0.968
7:99606763:G:AG75D0.964
7:99606766:G:CR76P0.963
7:99607810:G:CG165R0.963
7:99604494:T:CF36L0.962
7:99604496:C:AF36L0.962
7:99604496:C:GF36L0.962
7:99604542:G:CG52R0.962
7:99604543:G:AG52D0.961
7:99604572:T:AC62S0.959
7:99604573:G:CC62S0.959
7:99607702:C:GH129D0.957
7:99604559:C:GC57W0.956
7:99607762:T:AW149R0.956
7:99607762:T:CW149R0.956

dbSNP variants (sampled 300 via entrez): RS1000203657 (7:99606520 G>A), RS1000392694 (7:99599273 C>T), RS1000495177 (7:99611405 A>G), RS1000574168 (7:99606801 G>A), RS1000690957 (7:99605426 C>T), RS1000721649 (7:99605036 A>C), RS1000951387 (7:99611161 C>G,T), RS1001354869 (7:99601247 G>A), RS1001395635 (7:99600883 G>A), RS1001596655 (7:99598654 C>G), RS1001895795 (7:99597693 T>C), RS1002222906 (7:99609938 T>C,G), RS1002299286 (7:99596208 G>A), RS1002327131 (7:99597523 TTTA>T), RS1002360903 (7:99602739 G>A,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

10 total (human), top 10 by PubMed support.

ChemicalActions (top 5)PubMed papers
Nickeldecreases expression2
Valproic Acidaffects cotreatment, decreases expression2
benzo(e)pyrenedecreases methylation1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
abrineincreases expression1
dorsomorphinaffects cotreatment, decreases expression1
Air Pollutantsincreases abundance, increases expression1
Methapyrilenedecreases methylation1
Okadaic Aciddecreases expression1
Particulate Matterincreases abundance, increases 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.