TMEM184C

gene
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Also known as FLJ10846SLC51C3

Summary

TMEM184C (transmembrane protein 184C, HGNC:25587) is a protein-coding gene on chromosome 4q31.23, encoding Transmembrane protein 184C (Q9NVA4). Possible tumor suppressor which may play a role in cell growth.

Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be active in membrane.

Source: NCBI Gene 55751 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 46 total
  • MANE Select transcript: NM_018241

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25587
Approved symbolTMEM184C
Nametransmembrane protein 184C
Location4q31.23
Locus typegene with protein product
StatusApproved
AliasesFLJ10846, SLC51C3
Ensembl geneENSG00000164168
Ensembl biotypeprotein_coding
OMIM613937
Entrez55751

Gene structure

Transcript identifiers

Ensembl transcripts: 5 — 3 protein_coding, 1 nonsense_mediated_decay, 1 retained_intron

ENST00000296582, ENST00000505999, ENST00000506826, ENST00000508208, ENST00000880769

RefSeq mRNA: 1 — MANE Select: NM_018241 NM_018241

CCDS: CCDS3770

Canonical transcript exons

ENST00000296582 — 10 exons

ExonStartEnd
ENSE00001082022147623834147623964
ENSE00001082023147634169147636721
ENSE00001082024147631393147631505
ENSE00001082025147632903147633002
ENSE00001082026147624062147624098
ENSE00001082027147628361147628435
ENSE00001082028147629599147629692
ENSE00001082029147624804147625009
ENSE00002064092147617397147618079
ENSE00003635781147633765147633936

Expression profiles

Bgee: expression breadth ubiquitous, 259 present calls, max score 95.20.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 15.4916 / max 99.0617, expressed in 1804 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
4993514.11201800
499361.1802718
499370.134035
499380.065323

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
parotid glandUBERON:000183195.20silver quality
endothelial cellCL:000011594.80silver quality
hair follicleUBERON:000207394.37silver quality
buccal mucosa cellCL:000233694.25gold quality
mammary ductUBERON:000176592.39silver quality
adrenal tissueUBERON:001830392.09gold quality
heart right ventricleUBERON:000208091.76silver quality
epithelium of mammary glandUBERON:000324491.63silver quality
calcaneal tendonUBERON:000370191.37gold quality
lateral nuclear group of thalamusUBERON:000273691.03silver quality
stromal cell of endometriumCL:000225590.85gold quality
Brodmann (1909) area 23UBERON:001355490.77silver quality
mucosa of sigmoid colonUBERON:000499390.57gold quality
colonic mucosaUBERON:000031790.37gold quality
biceps brachiiUBERON:000150790.34silver quality
CA1 field of hippocampusUBERON:000388190.25silver quality
middle temporal gyrusUBERON:000277190.19gold quality
rectumUBERON:000105289.13gold quality
oviduct epitheliumUBERON:000480488.90gold quality
oocyteCL:000002388.72silver quality
corpus callosumUBERON:000233688.69gold quality
islet of LangerhansUBERON:000000688.61gold quality
smooth muscle tissueUBERON:000113588.59gold quality
thoracic mammary glandUBERON:000520088.57gold quality
mammary glandUBERON:000191188.53gold quality
placentaUBERON:000198788.53gold quality
thyroid glandUBERON:000204688.45gold quality
seminal vesicleUBERON:000099888.31gold quality
left lobe of thyroid glandUBERON:000112088.21gold quality
secondary oocyteCL:000065588.18gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes5.16
E-MTAB-6386no109.85

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

64 targeting TMEM184C, 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-3613-3P100.0076.367965
HSA-MIR-3120-5P100.0065.56965
HSA-MIR-3163100.0077.238605
HSA-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-98-3P100.0074.083907
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-1213699.9872.815713
HSA-MIR-806899.9873.852376
HSA-MIR-6499-3P99.9066.381212
HSA-MIR-6780A-5P99.8866.692776
HSA-MIR-4728-5P99.8569.394718
HSA-MIR-544A99.8468.661965
HSA-MIR-5010-3P99.8370.602357
HSA-MIR-6785-5P99.8268.684428
HSA-MIR-1273H-5P99.7766.322471
HSA-MIR-3617-5P99.7569.411968
HSA-MIR-64199.7569.351975
HSA-MIR-149-3P99.7268.223963
HSA-MIR-33A-3P99.7070.273362
HSA-MIR-30B-3P99.7065.762325
HSA-MIR-3689A-3P99.7065.732306
HSA-MIR-3689B-3P99.7065.712311
HSA-MIR-3689C99.7065.712311
HSA-MIR-6779-5P99.7065.762363
HSA-MIR-6883-5P99.6968.053785
HSA-MIR-1212499.6869.172700

Literature-anchored findings (GeneRIF, showing 1)

  • Recently, by cDNA microarray anal., we identified transmembrane protein 34 (TMEM34) that down-regulated in anaplastic thyroid cancer cell lines as compared to normal thyroid tissues. Transfection of TMEM34 into KTA2 cells led to inhibition of cell growth (PMID:17072649)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriotmem184cENSDARG00000078789
mus_musculusTmem184cENSMUSG00000031617
rattus_norvegicusTmem184cENSRNOG00000012860
drosophila_melanogasterCG5850FBGN0032172

Paralogs (3): SLC51A (ENSG00000163959), TMEM184A (ENSG00000164855), TMEM184B (ENSG00000198792)

Protein

Protein identifiers

Transmembrane protein 184CQ9NVA4 (reviewed: Q9NVA4)

Alternative names: Transmembrane protein 34

All UniProt accessions (3): A0A0C4DGC8, Q9NVA4, H0Y8I5

UniProt curated annotations — full annotation on UniProt →

Function. Possible tumor suppressor which may play a role in cell growth.

Subcellular location. Membrane.

Tissue specificity. Widely expressed with higher expression in lung, kidney, spleen, pancreas, thymus, prostate, testis, ovary, small intestine and thyroid.

Similarity. Belongs to the TMEM184 family.

Isoforms (2)

UniProt IDNamesCanonical?
Q9NVA4-11yes
Q9NVA4-22

RefSeq proteins (1): NP_060711* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR005178Ostalpha/TMEM184CFamily

Pfam: PF03619

UniProt features (18 total): transmembrane region 7, sequence conflict 4, compositionally biased region 3, chain 1, modified residue 1, splice variant 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9NVA4-F172.080.19

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (1): 422

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 93 (showing top): RUTELLA_RESPONSE_TO_CSF2RB_AND_IL4_UP, KINSEY_TARGETS_OF_EWSR1_FLII_FUSION_DN, GOBP_TRANSMEMBRANE_TRANSPORT, CAIRO_LIVER_DEVELOPMENT_UP, RUTELLA_RESPONSE_TO_HGF_UP, STEIN_ESRRA_TARGETS_UP, GOMF_TRANSPORTER_ACTIVITY, RUTELLA_RESPONSE_TO_HGF_VS_CSF2RB_AND_IL4_UP, GCM_RAB10, GSE14415_ACT_TCONV_VS_ACT_NATURAL_TREG_UP, CEBPZ_TARGET_GENES, DIDO1_TARGET_GENES, ELF2_TARGET_GENES, HDAC4_TARGET_GENES, ZNF350_TARGET_GENES

GO Biological Process (1): transmembrane transport (GO:0055085)

GO Molecular Function (1): transmembrane transporter activity (GO:0022857)

GO Cellular Component (1): membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
transport1
cellular process1
transporter activity1
transmembrane transport1
cellular anatomical structure1

Protein interactions and networks

STRING

622 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TMEM184CPRMT9Q6P2P2716
TMEM184CFAM204AQ9H8W3618
TMEM184CEDNRAP25101530
TMEM184CACBD6Q9BR61512
TMEM184CHSF2Q03933505
TMEM184CZCCHC9Q8N567476
TMEM184CFAM13BQ9NYF5469
TMEM184CTMEM207Q6UWW9465
TMEM184COR7E24Q6IFN5460
TMEM184CRAB11FIP2Q7L804443
TMEM184CPNISRQ8TF01435
TMEM184CKIF6Q6ZMV9427
TMEM184CTMEM214Q6NUQ4414
TMEM184CSLC35A4Q96G79411
TMEM184CCOL23A1Q86Y22400

IntAct

13 interactions, top by confidence:

ABTypeScore
SGK1TMEM184Cpsi-mi:“MI:0915”(physical association)0.370
ESYT2psi-mi:“MI:0914”(association)0.350
E5ESYT2psi-mi:“MI:0914”(association)0.350
Npc1ESYT2psi-mi:“MI:0914”(association)0.350
LAMP1DSTpsi-mi:“MI:0914”(association)0.350
LAMTOR2SCAMP3psi-mi:“MI:0914”(association)0.350
MAPRE1SCAMP1psi-mi:“MI:0914”(association)0.350
POLR1DBDP1psi-mi:“MI:0914”(association)0.350
STX7SCAMP1psi-mi:“MI:0914”(association)0.350
TNFRSF10CPLPP3psi-mi:“MI:0914”(association)0.350
TCTN3TMEM120Bpsi-mi:“MI:2364”(proximity)0.270

BioGRID (22): TMEM184C (Proximity Label-MS), TMEM184C (Synthetic Lethality), TMEM184C (Affinity Capture-MS), TMEM184C (Affinity Capture-MS), TMEM184C (Affinity Capture-MS), TMEM184C (Proximity Label-MS), TMEM184C (Affinity Capture-MS), TMEM184C (Affinity Capture-MS), TMEM184C (Affinity Capture-MS), TMEM184C (Affinity Capture-MS), TMEM184C (Affinity Capture-MS), TMEM184C (Affinity Capture-MS), TMEM184C (Cross-Linking-MS (XL-MS)), TMEM184C (Affinity Capture-MS), TMEM184C (Co-fractionation)

ESM2 similar proteins: A0JNC1, A0PK00, A1L2R7, A2BIE7, A3KNK1, A6QPF8, A7XZ53, A8DZH4, D3ZEH5, O35052, O95427, P98191, Q05B45, Q0VFK3, Q17QL9, Q1LY80, Q28CY9, Q3TA38, Q5BL21, Q5EAX9, Q5EAY8, Q5FWV6, Q5HZE2, Q5RET6, Q5U239, Q5ZMP3, Q63ZG0, Q68EY2, Q6DD44, Q6DE21, Q6ZMG9, Q7ZUA6, Q8BXA5, Q8C172, Q8C1E7, Q8CIF6, Q8NBJ9, Q8WVP7, Q91XU8, Q92903

Diamond homologs: A2VDL9, Q09906, Q17QL9, Q1RMW2, Q28CV2, Q3TPR7, Q3UFJ6, Q4QQS1, Q54PI4, Q54WM0, Q5BPZ5, Q5RET6, Q5ZMP3, Q6GQE1, Q6ZMB5, Q75JN3, Q810F5, Q8BG09, Q9NVA4, Q9Y519, F4JTN2, Q94CA0, P36142

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance30
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

2592 predictions. Top by Δscore:

VariantEffectΔscore
4:147623828:CTTAA:Cacceptor_loss1.0000
4:147623829:TTAA:Tacceptor_loss1.0000
4:147623832:A:Gacceptor_gain1.0000
4:147623833:G:Cacceptor_loss1.0000
4:147623962:AAGGT:Adonor_loss1.0000
4:147623964:GGTA:Gdonor_loss1.0000
4:147624057:AATAG:Aacceptor_gain1.0000
4:147624094:ATAGT:Adonor_gain1.0000
4:147624095:TAGT:Tdonor_gain1.0000
4:147624097:GT:Gdonor_gain1.0000
4:147624099:G:GGdonor_gain1.0000
4:147624800:ATAGT:Aacceptor_gain1.0000
4:147624802:A:AGacceptor_gain1.0000
4:147624802:AGT:Aacceptor_gain1.0000
4:147624802:AGTG:Aacceptor_gain1.0000
4:147624803:G:GGacceptor_gain1.0000
4:147624803:GT:Gacceptor_gain1.0000
4:147624803:GTG:Gacceptor_gain1.0000
4:147624803:GTGG:Gacceptor_gain1.0000
4:147625005:GGAGA:Gdonor_gain1.0000
4:147625006:GAGAG:Gdonor_gain1.0000
4:147625008:GA:Gdonor_gain1.0000
4:147625010:G:GGdonor_gain1.0000
4:147628359:A:AGacceptor_gain1.0000
4:147628360:G:GGacceptor_gain1.0000
4:147628360:GA:Gacceptor_gain1.0000
4:147628360:GAGT:Gacceptor_gain1.0000
4:147628360:GAGTA:Gacceptor_gain1.0000
4:147628431:GCTTT:Gdonor_gain1.0000
4:147628433:TTT:Tdonor_gain1.0000

AlphaMissense

2851 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
4:147623950:A:CQ80H0.999
4:147623950:A:TQ80H0.999
4:147624069:T:AW88R0.999
4:147624069:T:CW88R0.999
4:147624087:A:CS94R0.999
4:147624089:T:AS94R0.999
4:147624089:T:GS94R0.999
4:147624854:A:CR114S0.999
4:147624854:A:TR114S0.999
4:147631409:T:CL228P0.999
4:147631501:T:CF259L0.999
4:147631503:T:AF259L0.999
4:147631503:T:GF259L0.999
4:147633788:G:AM301I0.999
4:147633788:G:CM301I0.999
4:147633788:G:TM301I0.999
4:147633819:T:CF312L0.999
4:147633821:C:AF312L0.999
4:147633821:C:GF312L0.999
4:147623964:G:TR85M0.998
4:147624073:T:CM89T0.998
4:147624073:T:GM89R0.998
4:147624804:T:AW98R0.998
4:147624804:T:CW98R0.998
4:147624853:G:CR114T0.998
4:147624853:G:TR114I0.998
4:147624865:A:TE118V0.998
4:147624898:T:CL129P0.998
4:147628386:G:CG175R0.998
4:147628387:G:AG175D0.998

dbSNP variants (sampled 300 via entrez): RS1000551635 (4:147632078 CAGG>C), RS1000622543 (4:147630103 T>C), RS1000883621 (4:147636543 G>T), RS1000899940 (4:147632401 A>G), RS1000944682 (4:147630428 A>T), RS1001093606 (4:147618709 C>A,T), RS1001667848 (4:147631967 G>A), RS1001705919 (4:147635644 T>C,G), RS1001722009 (4:147631787 A>G), RS1002111023 (4:147621948 T>C), RS1002222701 (4:147629216 C>T), RS1002354024 (4:147621485 A>T), RS1002494302 (4:147629944 T>G), RS1002555319 (4:147635117 CG>C), RS1002858881 (4:147621196 T>C)

Disease associations

OMIM: gene MIM:613937 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

1 associations (top):

StudyTraitp-value
GCST002960_3Frontotemporal dementia3.000000e-06

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

23 total (human), top 23 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arsenitedecreases expression, increases expression2
Cadmium Chlorideincreases abundance, increases palmitoylation, decreases expression, decreases reaction2
aristolochic acid Idecreases expression1
FR900359increases phosphorylation1
triphenyl phosphateaffects expression1
2-bromopalmitatedecreases reaction, increases abundance, increases palmitoylation1
N,N,N’,N’-tetrakis(2-pyridylmethyl)ethylenediamineincreases expression1
di-n-butylphosphoric acidaffects expression1
Temozolomidedecreases expression1
Air Pollutantsdecreases expression, increases abundance1
Air Pollutants, Occupationaldecreases expression1
Cadmiumdecreases reaction, increases abundance, increases palmitoylation1
Formaldehydeincreases expression1
Hydrogen Peroxidedecreases expression1
Leadincreases expression1
Nickeldecreases expression1
Phthalic Acidsincreases methylation1
Smokedecreases expression1
Urethaneincreases expression1
Aflatoxin B1increases methylation1
Sodium Seleniteincreases expression1
Zinc Sulfatedecreases expression1
Particulate Matterdecreases expression, increases abundance1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): frontotemporal dementia