TMEM234

gene
On this page

Also known as RP4-622L5dJ622L5.7FLJ90779

Summary

TMEM234 (transmembrane protein 234, HGNC:28837) is a protein-coding gene on chromosome 1p35.2, encoding Transmembrane protein 234 (Q8WY98).

Predicted to be located in membrane.

Source: NCBI Gene 56063 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 14 total
  • MANE Select transcript: NM_019118

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:28837
Approved symbolTMEM234
Nametransmembrane protein 234
Location1p35.2
Locus typegene with protein product
StatusApproved
AliasesRP4-622L5, dJ622L5.7, FLJ90779
Ensembl geneENSG00000160055
Ensembl biotypeprotein_coding
OMIM620289
Entrez56063

Gene structure

Transcript identifiers

Ensembl transcripts: 12 — 4 protein_coding, 3 nonsense_mediated_decay, 3 protein_coding_CDS_not_defined, 2 retained_intron

ENST00000309777, ENST00000344461, ENST00000373593, ENST00000461402, ENST00000466796, ENST00000483001, ENST00000484490, ENST00000485689, ENST00000487174, ENST00000489170, ENST00000491434, ENST00000495091

RefSeq mRNA: 2 — MANE Select: NM_019118 NM_001366191, NM_019118

CCDS: CCDS356, CCDS90906

Canonical transcript exons

ENST00000309777 — 5 exons

ExonStartEnd
ENSE000014609823221620032216947
ENSE000016752373222230732222353
ENSE000017807573222186732222018
ENSE000036516543222113132221197
ENSE000036837633221725932217351

Expression profiles

Bgee: expression breadth ubiquitous, 220 present calls, max score 97.05.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 7.9889 / max 104.1237, expressed in 1789 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
115177.67441789
115160.3145148

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right uterine tubeUBERON:000130297.05gold quality
buccal mucosa cellCL:000233693.05gold quality
tendon of biceps brachiiUBERON:000818892.71gold quality
right lobe of thyroid glandUBERON:000111992.47gold quality
left lobe of thyroid glandUBERON:000112091.98gold quality
adenohypophysisUBERON:000219691.80gold quality
thyroid glandUBERON:000204690.86gold quality
pituitary glandUBERON:000000790.60gold quality
left testisUBERON:000453389.22gold quality
right testisUBERON:000453488.74gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047388.34gold quality
metanephros cortexUBERON:001053388.14gold quality
mucosa of transverse colonUBERON:000499187.38gold quality
testisUBERON:000047386.97gold quality
body of uterusUBERON:000985386.43gold quality
endocervixUBERON:000045886.30gold quality
right adrenal glandUBERON:000123386.28gold quality
right adrenal gland cortexUBERON:003582785.99gold quality
left ovaryUBERON:000211985.97gold quality
tibialis anteriorUBERON:000138585.59gold quality
right ovaryUBERON:000211885.59gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099185.54gold quality
left uterine tubeUBERON:000130385.53gold quality
ileal mucosaUBERON:000033185.37gold quality
granulocyteCL:000009485.17gold quality
left adrenal glandUBERON:000123485.07gold quality
lower esophagus mucosaUBERON:003583485.07gold quality
left adrenal gland cortexUBERON:003582585.04gold quality
olfactory segment of nasal mucosaUBERON:000538684.84gold quality
left coronary arteryUBERON:000162684.81gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes6.53

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

36 targeting TMEM234, 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-4283100.0066.422097
HSA-MIR-450099.9972.722367
HSA-MIR-34A-5P99.9971.211784
HSA-MIR-449A99.9971.051776
HSA-LET-7A-5P99.9872.291790
HSA-LET-7B-5P99.9872.311790
HSA-LET-7C-5P99.9872.291790
HSA-LET-7E-5P99.9872.291790
HSA-LET-7F-5P99.9872.561784
HSA-LET-7G-5P99.9872.371784
HSA-LET-7I-5P99.9872.371788
HSA-MIR-98-5P99.9872.331787
HSA-MIR-4650-5P99.9864.69999
HSA-LET-7D-5P99.9671.761632
HSA-MIR-445899.9671.641650
HSA-MIR-448799.9664.581252
HSA-MIR-6809-3P99.9171.453814
HSA-MIR-449299.8768.253611
HSA-MIR-383-3P99.8565.841359
HSA-MIR-202-3P99.8471.411290
HSA-MIR-7156-5P99.6468.811369
HSA-MIR-486-3P99.5166.821901
HSA-MIR-427399.4567.931206
HSA-MIR-616599.4467.121389
HSA-MIR-450599.2767.812678
HSA-MIR-149-5P99.2567.161315
HSA-MIR-578799.2267.862628
HSA-MIR-5001-3P98.9167.281394
HSA-MIR-3074-5P98.8266.561414
HSA-MIR-3135B98.6165.331470

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusTmem234ENSMUSG00000028797
rattus_norvegicusTmem234ENSRNOG00000049326

Protein

Protein identifiers

Transmembrane protein 234Q8WY98 (reviewed: Q8WY98)

All UniProt accessions (2): Q8WY98, E9PNU5

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Miscellaneous. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay.

Similarity. Belongs to the TMEM234 family.

Isoforms (4)

UniProt IDNamesCanonical?
Q8WY98-11yes
Q8WY98-22
Q8WY98-33
Q8WY98-44

RefSeq proteins (2): NP_001353120, NP_061991* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR018908TMEM234Family
IPR037185EmrE-likeHomologous_superfamily

Pfam: PF10639

UniProt features (10 total): splice variant 5, transmembrane region 3, chain 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8WY98-F184.590.49

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 65 (showing top): MARTINEZ_RB1_TARGETS_UP, LASTOWSKA_NEUROBLASTOMA_COPY_NUMBER_DN, MARTINEZ_RB1_AND_TP53_TARGETS_UP, chr1p35, DODD_NASOPHARYNGEAL_CARCINOMA_DN, ZWANG_TRANSIENTLY_UP_BY_2ND_EGF_PULSE_ONLY, GSE13522_CTRL_VS_T_CRUZI_BRAZIL_STRAIN_INF_SKIN_UP, GSE5503_PLN_DC_VS_SPLEEN_DC_ACTIVATED_ALLOGENIC_TCELL_DN, ELF2_TARGET_GENES, FOXN3_TARGET_GENES, FOXR2_TARGET_GENES, NKX2_2_TARGET_GENES, ZNF664_TARGET_GENES, MIR4500, LET_7B_5P

GO Biological Process (0):

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
binding1
cellular anatomical structure1

Protein interactions and networks

STRING

302 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM234TMEM144Q7Z5S9507
TMEM234TCP11L2Q8N4U5462
TMEM234CCDC28BQ9BUN5460
TMEM234ZNF185O15231459
TMEM234XKRXQ6PP77455
TMEM234TMEM63CQ9P1W3453
TMEM234TMEM63BQ5T3F8436
TMEM234EFCC1Q9HA90431
TMEM234TMEM63AO94886426
TMEM234SPMIP5Q8WW14418
TMEM234MMADHCQ9H3L0396
TMEM234RPP21Q9H633392
TMEM234TCEAL8Q8IYN2370
TMEM234TXLNAP40222357
TMEM234LRRC49Q8IUZ0354

IntAct

50 interactions, top by confidence:

ABTypeScore
CREB3L1TMEM234psi-mi:“MI:0915”(physical association)0.560
TMEM234CREB3L1psi-mi:“MI:0915”(physical association)0.560
FAM241BTMEM234psi-mi:“MI:0915”(physical association)0.560
CXCL9TMEM234psi-mi:“MI:0915”(physical association)0.560
TMEM203TMEM234psi-mi:“MI:0915”(physical association)0.560
TMEM218TMEM234psi-mi:“MI:0915”(physical association)0.560
VTI1BTMEM234psi-mi:“MI:0915”(physical association)0.560
BRICD5TMEM234psi-mi:“MI:0915”(physical association)0.560
TMEM107TMEM234psi-mi:“MI:0915”(physical association)0.560
TMEM234VTI1Bpsi-mi:“MI:0915”(physical association)0.560
SLC10A6TMEM234psi-mi:“MI:0915”(physical association)0.560
SLC10A1TMEM234psi-mi:“MI:0915”(physical association)0.560
TMEM234FAM241Bpsi-mi:“MI:0915”(physical association)0.560
SLC34A3TMEM234psi-mi:“MI:0915”(physical association)0.560
TMEM234TMEM203psi-mi:“MI:0915”(physical association)0.560
SLC35E3TMEM234psi-mi:“MI:0915”(physical association)0.560
SMAGPTMEM234psi-mi:“MI:0915”(physical association)0.560
UNC50TMEM234psi-mi:“MI:0915”(physical association)0.560

BioGRID (19): CREB3L1 (Two-hybrid), TMEM234 (Two-hybrid), TMEM234 (Two-hybrid), TMEM234 (Two-hybrid), TMEM234 (Two-hybrid), TMEM234 (Two-hybrid), TMEM234 (Two-hybrid), TMEM234 (Two-hybrid), TMEM234 (Two-hybrid), TMEM234 (Two-hybrid), SMAGP (Two-hybrid), C10orf35 (Two-hybrid), SLC35E3 (Two-hybrid), TMEM107 (Two-hybrid), BRICD5 (Two-hybrid)

ESM2 similar proteins: A0NGI1, A7YW81, O74750, O94654, P40004, Q00974, Q02334, Q03730, Q04083, Q09875, Q0D2K0, Q0V9U2, Q10000, Q29Q28, Q3E6T0, Q3SWX0, Q54V96, Q54ZG7, Q550W6, Q55FV8, Q5R7Q3, Q5T1Q4, Q6CR04, Q6FSF8, Q7RTP0, Q7TML3, Q8BGK5, Q8BHK1, Q8BLX4, Q8BMW7, Q8BZF2, Q8IXU6, Q8MXJ9, Q8N8Q9, Q8R1E7, Q8WY98, Q94EI9, Q968A5, Q9C8M1, Q9JJC8

Diamond homologs: A0NGI1, A7YW81, Q54ZG7, Q5RBQ9, Q8R1E7, Q8WY98

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance9
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1537 predictions. Top by Δscore:

VariantEffectΔscore
1:32215435:TTTA:Tacceptor_loss1.0000
1:32215437:TA:Tacceptor_loss1.0000
1:32215438:A:ACacceptor_loss1.0000
1:32215438:A:AGacceptor_gain1.0000
1:32215439:G:GGacceptor_gain1.0000
1:32221198:C:CCacceptor_gain1.0000
1:32222115:T:TAdonor_gain1.0000
1:32215438:AG:Aacceptor_gain0.9900
1:32215439:GG:Gacceptor_gain0.9900
1:32215439:GGA:Gacceptor_gain0.9900
1:32215439:GGAGT:Gacceptor_gain0.9900
1:32217361:C:CTacceptor_gain0.9900
1:32221126:CCCA:Cdonor_loss0.9900
1:32221127:CCA:Cdonor_loss0.9900
1:32221128:CA:Cdonor_loss0.9900
1:32221129:A:ATdonor_loss0.9900
1:32221195:GTA:Gacceptor_gain0.9900
1:32221196:TA:Tacceptor_gain0.9900
1:32221196:TACTG:Tacceptor_loss0.9900
1:32221197:ACT:Aacceptor_loss0.9900
1:32221198:CT:Cacceptor_loss0.9900
1:32221862:CGCA:Cdonor_loss0.9900
1:32221863:GCA:Gdonor_loss0.9900
1:32221864:CAC:Cdonor_loss0.9900
1:32221865:A:Cdonor_loss0.9900
1:32222119:T:TAdonor_gain0.9900
1:32215436:TTAGG:Tacceptor_gain0.9800
1:32215437:TAGG:Tacceptor_gain0.9800
1:32215438:AGGA:Aacceptor_gain0.9800
1:32215439:GGAG:Gacceptor_gain0.9800

AlphaMissense

871 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
1:32221983:A:GW18R0.976
1:32221983:A:TW18R0.976
1:32221991:G:TA15D0.974
1:32221981:C:AW18C0.971
1:32221981:C:GW18C0.971
1:32217323:G:CN88K0.970
1:32217323:G:TN88K0.970
1:32217326:A:CC87W0.966
1:32221166:C:TG67E0.966
1:32217328:A:GC87R0.960
1:32221174:G:CN64K0.959
1:32221174:G:TN64K0.959
1:32221957:C:AK26N0.958
1:32221957:C:GK26N0.958
1:32216914:C:TG121E0.956
1:32217327:C:TC87Y0.954
1:32221980:C:GG19R0.954
1:32221170:A:GC66R0.953
1:32217339:G:TA83D0.951
1:32221988:G:TA16D0.951
1:32217294:A:TV98D0.944
1:32221176:T:CN64D0.944
1:32221155:A:CY71D0.942
1:32221197:A:GY57H0.941
1:32216935:C:TG114D0.938
1:32221979:C:TG19D0.937
1:32221142:A:GL75S0.935
1:32221183:A:CF61L0.932
1:32221183:A:TF61L0.932
1:32221185:A:GF61L0.932

dbSNP variants (sampled 300 via entrez): RS1000559671 (1:32222834 C>A,G), RS1000621551 (1:32221435 A>T), RS1000713531 (1:32216362 T>C), RS1000940977 (1:32220165 T>C,G), RS1001605814 (1:32223102 C>T), RS1002415761 (1:32217620 C>A), RS1002479267 (1:32215275 G>A,C), RS1003082877 (1:32218130 G>C), RS1003162909 (1:32219325 T>C), RS1004169343 (1:32215158 GC>G,GCC), RS1004436057 (1:32220733 T>A,C), RS1004657952 (1:32215164 G>A), RS1005013841 (1:32219427 C>G), RS1005249336 (1:32216282 C>G,T), RS1005260110 (1:32216537 G>C,T)

Disease associations

OMIM: gene MIM:620289 | 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

25 total (human), top 25 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arseniteaffects cotreatment, decreases expression, increases abundance, increases expression2
Methyl Methanesulfonateincreases expression2
aristolochic acid Idecreases expression1
triphenyl phosphateaffects expression1
manganese chloridedecreases expression, increases abundance, affects cotreatment1
1-hydroxypyrenedecreases expression1
2-palmitoylglycerolincreases expression1
abrineincreases expression1
jinfukangaffects cotreatment, increases expression1
Air Pollutantsaffects expression, increases abundance1
Air Pollutants, Occupationaldecreases expression1
Arsenicincreases abundance, affects cotreatment, decreases expression1
Cisplatinaffects cotreatment, increases expression1
Doxorubicindecreases expression1
Manganesedecreases expression, increases abundance, affects cotreatment1
Ozoneincreases abundance, affects expression1
Smokedecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Tretinoinincreases expression1
Valproic Acidincreases methylation1
Aflatoxin B1increases methylation1
Cadmium Chlorideincreases expression1
Copper Sulfatedecreases expression1
Acrylamidedecreases expression1
Particulate Matterdecreases 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.