SLC16A14

gene
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Also known as FLJ30794MCT14

Summary

SLC16A14 (solute carrier family 16 member 14, HGNC:26417) is a protein-coding gene on chromosome 2q36.3, encoding Monocarboxylate transporter 14 (Q7RTX9). Proton-linked monocarboxylate transporter.

Predicted to enable monocarboxylic acid transmembrane transporter activity. Predicted to be involved in carboxylic acid transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane.

Source: NCBI Gene 151473 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 37 total
  • MANE Select transcript: NM_152527

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26417
Approved symbolSLC16A14
Namesolute carrier family 16 member 14
Location2q36.3
Locus typegene with protein product
StatusApproved
AliasesFLJ30794, MCT14
Ensembl geneENSG00000163053
Ensembl biotypeprotein_coding
Entrez151473

Gene structure

Transcript identifiers

Ensembl transcripts: 11 — 11 protein_coding

ENST00000295190, ENST00000412034, ENST00000425822, ENST00000436869, ENST00000457406, ENST00000880804, ENST00000880805, ENST00000880806, ENST00000880807, ENST00000880808, ENST00000920474

RefSeq mRNA: 1 — MANE Select: NM_152527 NM_152527

CCDS: CCDS2473

Canonical transcript exons

ENST00000295190 — 5 exons

ExonStartEnd
ENSE00001071163230034982230037531
ENSE00001174939230045745230046722
ENSE00001343653230068555230068924
ENSE00001382609230049761230049904
ENSE00001387951230059094230059366

Expression profiles

Bgee: expression breadth ubiquitous, 244 present calls, max score 99.04.

FANTOM5 (CAGE): breadth broad, TPM avg 2.4765 / max 56.8238, expressed in 612 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
344432.1873581
344440.127665
344410.081836
344420.079942

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
pigmented layer of retinaUBERON:000178299.04gold quality
retinaUBERON:000096699.01gold quality
endothelial cellCL:000011597.33gold quality
middle temporal gyrusUBERON:000277194.03gold quality
Brodmann (1909) area 23UBERON:001355493.60gold quality
cerebellar vermisUBERON:000472091.76gold quality
parotid glandUBERON:000183189.76gold quality
skin of hipUBERON:000155489.43gold quality
Brodmann (1909) area 46UBERON:000648389.37gold quality
cortical plateUBERON:000534389.16gold quality
upper leg skinUBERON:000426288.70gold quality
upper arm skinUBERON:000426388.01gold quality
lateral nuclear group of thalamusUBERON:000273686.51gold quality
superior frontal gyrusUBERON:000266186.06gold quality
ponsUBERON:000098885.84gold quality
primary visual cortexUBERON:000243685.67gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047385.60gold quality
visceral pleuraUBERON:000240185.51gold quality
ganglionic eminenceUBERON:000402385.13gold quality
cauda epididymisUBERON:000436084.95gold quality
postcentral gyrusUBERON:000258184.91gold quality
occipital lobeUBERON:000202184.86gold quality
entorhinal cortexUBERON:000272884.67gold quality
parietal lobeUBERON:000187284.62gold quality
esophagus squamous epitheliumUBERON:000692084.19gold quality
palpebral conjunctivaUBERON:000181282.56gold quality
parietal pleuraUBERON:000240082.37gold quality
prefrontal cortexUBERON:000045182.18gold quality
ventricular zoneUBERON:000305381.41gold quality
frontal cortexUBERON:000187080.94gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-GEOD-135922yes13.45
E-ANND-3no0.00

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

116 targeting SLC16A14, 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-29A-3P100.0073.111835
HSA-MIR-29B-3P100.0073.181833
HSA-MIR-29C-3P100.0073.151833
HSA-MIR-3689D100.0066.141181
HSA-MIR-6851-5P100.0065.631294
HSA-MIR-6867-5P100.0082.213464
HSA-MIR-5011-5P100.0083.465820
HSA-MIR-656-3P100.0072.152788
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-30A-5P100.0076.313233
HSA-MIR-30B-5P100.0076.293248
HSA-MIR-30C-5P100.0076.293248
HSA-MIR-30D-5P100.0076.323233
HSA-MIR-30E-5P100.0076.323242
HSA-MIR-3646100.0073.565283
HSA-MIR-450099.9972.722367
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-196A-1-3P99.9972.152772
HSA-MIR-223-3P99.9970.141140
HSA-MIR-480399.9871.993117
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
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

Literature-anchored findings (GeneRIF, showing 1)

  • Study presented a phylogenetic analysis revealing that Slc16a14 is closely related to Slc16a2, Slc16a9 and Slc16a10; provided a detailed expression analysis of Slc16a14 expression, finding widespread expression in the mouse brain and establishing its expression in neurons and epithelial cells. QRT-PCR on a panel of mouse tissues revealed high Slc16a14 expression in the kidney and moderate levels in the CNS. (PMID:27364523)

Cross-species orthologs

16 orthologs

OrganismSymbolGene ID
mus_musculusSlc16a14ENSMUSG00000026220
rattus_norvegicusSlc16a14ENSRNOG00000017072
drosophila_melanogasterMct1FBGN0023549
drosophila_melanogasterCG14196FBGN0031002
drosophila_melanogasterCG8051FBGN0031012
drosophila_melanogasterSlnFBGN0033657
drosophila_melanogasterCG8468FBGN0033913
drosophila_melanogasterTargFBGN0033955
drosophila_melanogasterCG13907FBGN0035173
drosophila_melanogasteroutFBGN0259834
caenorhabditis_elegansWBGENE00003986
caenorhabditis_elegansWBGENE00010834
caenorhabditis_elegansWBGENE00015273
caenorhabditis_elegansWBGENE00015676
caenorhabditis_elegansWBGENE00020168
caenorhabditis_elegansWBGENE00021227

Paralogs (13): SLC16A8 (ENSG00000100156), SLC16A6 (ENSG00000108932), SLC16A10 (ENSG00000112394), SLC16A7 (ENSG00000118596), SLC16A3 (ENSG00000141526), SLC16A2 (ENSG00000147100), SLC16A12 (ENSG00000152779), SLC16A1 (ENSG00000155380), SLC16A9 (ENSG00000165449), SLC16A4 (ENSG00000168679), SLC16A5 (ENSG00000170190), SLC16A11 (ENSG00000174326), SLC16A13 (ENSG00000174327)

Protein

Protein identifiers

Monocarboxylate transporter 14Q7RTX9 (reviewed: Q7RTX9)

Alternative names: Solute carrier family 16 member 14

All UniProt accessions (5): C9JIV1, C9JME4, E7EMG7, Q7RTX9, Q6ZWE5

UniProt curated annotations — full annotation on UniProt →

Function. Proton-linked monocarboxylate transporter. May catalyze the transport of monocarboxylates across the plasma membrane.

Subcellular location. Cell membrane.

Similarity. Belongs to the major facilitator superfamily. Monocarboxylate porter (TC 2.A.1.13) family.

Isoforms (2)

UniProt IDNamesCanonical?
Q7RTX9-11yes
Q7RTX9-22

RefSeq proteins (1): NP_689740* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR011701MFSFamily
IPR020846MFS_domDomain
IPR036259MFS_trans_sfHomologous_superfamily
IPR050327Proton-linked_MCTFamily

Pfam: PF07690

UniProt features (19 total): transmembrane region 12, topological domain 2, chain 1, region of interest 1, compositionally biased region 1, splice variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q7RTX9-F179.820.50

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 109 (showing top): TGGTGCT_MIR29A_MIR29B_MIR29C, NKX25_02, PEREZ_TP63_TARGETS, GOZGIT_ESR1_TARGETS_DN, GOBP_ORGANIC_ACID_TRANSPORT, YAGUE_PRETUMOR_DRUG_RESISTANCE_UP, GOBP_ORGANIC_ANION_TRANSPORT, NAKAMURA_TUMOR_ZONE_PERIPHERAL_VS_CENTRAL_DN, GOBP_MONOCARBOXYLIC_ACID_TRANSPORT, AACTTT_UNKNOWN, PEREZ_TP53_AND_TP63_TARGETS, JAATINEN_HEMATOPOIETIC_STEM_CELL_UP, TGCCTTA_MIR124A, GOBP_TRANSMEMBRANE_TRANSPORT, NUYTTEN_EZH2_TARGETS_DN

GO Biological Process (3): carboxylic acid transmembrane transport (GO:1905039), monocarboxylic acid transport (GO:0015718), transmembrane transport (GO:0055085)

GO Molecular Function (3): monocarboxylic acid transmembrane transporter activity (GO:0008028), symporter activity (GO:0015293), transmembrane transporter activity (GO:0022857)

GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
carboxylic acid transport2
transmembrane transport2
transport1
cellular process1
monocarboxylic acid transport1
carboxylic acid transmembrane transporter activity1
secondary active transmembrane transporter activity1
transporter activity1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

528 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SLC16A14ZNF575Q86XF7503
SLC16A14SLC5A12Q1EHB4492
SLC16A14SLC5A8Q8N695487
SLC16A14BSGP35613473
SLC16A14PRELID3BQ9Y3B1451
SLC16A14EMBQ6PCB8448
SLC16A14CYYR1Q96J86428
SLC16A14PDK4Q16654406
SLC16A14BLOC1S6Q9UL45404
SLC16A14CMBLQ96DG6401
SLC16A14IP6K1Q92551396
SLC16A14IRF9Q00978388
SLC16A14JOSD1Q15040387
SLC16A14KCNIP3Q9Y2W7387
SLC16A14HCAR1Q9BXC0380

IntAct

3 interactions, top by confidence:

ABTypeScore
SLC16A14GNAQpsi-mi:“MI:0914”(association)0.350
SLC16A14MT-ATP8psi-mi:“MI:0914”(association)0.350

BioGRID (12): GNAQ (Affinity Capture-MS), YES1 (Affinity Capture-MS), GNAQ (Affinity Capture-MS), SVIP (Affinity Capture-MS), SLC16A14 (Affinity Capture-RNA), SLC16A14 (Affinity Capture-MS), ANKRD13A (Affinity Capture-MS), APOB (Affinity Capture-MS), BSG (Affinity Capture-MS), CLCC1 (Affinity Capture-MS), ATP8 (Affinity Capture-MS), SPPL3 (Affinity Capture-MS)

ESM2 similar proteins: A0A6I8PMZ8, A1Z7R6, A4IHK6, A4QN56, A7Y2X0, A9JTG4, B1AT66, B2RXV4, F5H094, M0RCI4, O15403, O75387, P34711, P58295, P81721, Q08280, Q08C75, Q0VCM6, Q497L8, Q5BIZ0, Q5R5M4, Q5RCN7, Q5RF58, Q5ZJU0, Q5ZJZ4, Q68EU6, Q6A4L1, Q6PDC8, Q761V0, Q7RTX9, Q7RTY1, Q7SXB7, Q7TM99, Q7TMR7, Q86UG4, Q8BSM7, Q8C0X7, Q8CGA3, Q8K1C7, Q8N370

Diamond homologs: A0LNN5, B1AT66, G5E8K6, O15375, O35308, Q7RTX9, Q7TMR7, Q8K1C7, A1L1W9, G8XYX6, O15374, O70324, P36021, Q3U9N9, Q8K1P8, Q8R0M8, Q8TF71, Q91Y77, A0A2U8U2M7, M0RCI4, O35440, O70451, P53988, Q17QR6, Q5R5M4, Q5ZJU0, Q63344, Q66HE2, Q7RTY0, Q7RTY1, Q7TM99, Q8CE94, A0KGK4, A4SR87, D4A734, O15403, O15427, O35910, O60669, O70461

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance32
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

952 predictions. Top by Δscore:

VariantEffectΔscore
2:230046721:GC:Gacceptor_gain1.0000
2:230046722:CC:Cacceptor_gain1.0000
2:230046723:C:CCacceptor_gain1.0000
2:230046733:C:CTacceptor_gain1.0000
2:230046733:C:Tacceptor_gain1.0000
2:230046734:G:Tacceptor_gain1.0000
2:230046736:C:CTacceptor_gain1.0000
2:230046737:G:Tacceptor_gain1.0000
2:230049755:GCTT:Gdonor_loss1.0000
2:230049756:CTTA:Cdonor_loss1.0000
2:230049757:TTA:Tdonor_loss1.0000
2:230049758:TAC:Tdonor_loss1.0000
2:230049759:A:ACdonor_gain1.0000
2:230049760:C:CCdonor_gain1.0000
2:230049760:CCAG:Cdonor_gain1.0000
2:230068551:TCA:Tdonor_loss1.0000
2:230068553:ACCG:Adonor_gain1.0000
2:230068553:ACCGC:Adonor_gain1.0000
2:230068554:CCG:Cdonor_gain1.0000
2:230068554:CCGC:Cdonor_gain1.0000
2:230068554:CCGCC:Cdonor_gain1.0000
2:230045739:GTTTA:Gdonor_loss0.9900
2:230045741:TTACC:Tdonor_loss0.9900
2:230045742:TA:Tdonor_loss0.9900
2:230045743:A:AGdonor_loss0.9900
2:230045744:C:CTdonor_loss0.9900
2:230046718:CAGGC:Cacceptor_gain0.9900
2:230046719:AGGC:Aacceptor_gain0.9900
2:230046720:GGC:Gacceptor_gain0.9900
2:230046725:G:Cacceptor_gain0.9900

AlphaMissense

3361 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
2:230045777:C:TG450D0.998
2:230045778:C:GG450R0.998
2:230046116:A:GL337P0.997
2:230046634:G:CS164R0.997
2:230046634:G:TS164R0.997
2:230046636:T:GS164R0.997
2:230046667:G:CF153L0.997
2:230046667:G:TF153L0.997
2:230046669:A:GF153L0.997
2:230059172:A:GW61R0.997
2:230059172:A:TW61R0.997
2:230045760:C:GG456R0.996
2:230045760:C:TG456R0.996
2:230045869:A:CS419R0.996
2:230045869:A:TS419R0.996
2:230045871:T:GS419R0.996
2:230045879:C:TG416E0.996
2:230049813:A:CS117R0.996
2:230049813:A:TS117R0.996
2:230049815:T:GS117R0.996
2:230045880:C:AG416W0.995
2:230045880:C:GG416R0.995
2:230045880:C:TG416R0.995
2:230046047:G:TA360E0.995
2:230046139:G:CS329R0.995
2:230046139:G:TS329R0.995
2:230046141:T:GS329R0.995
2:230046627:C:AG167W0.995
2:230059208:C:GG49R0.995
2:230046626:C:TG167E0.994

dbSNP variants (sampled 300 via entrez): RS1000372846 (2:230064017 A>G), RS1000413305 (2:230050531 A>G), RS1000500895 (2:230062930 C>T), RS1000541602 (2:230053086 T>G), RS1000641746 (2:230045440 A>C), RS1000763038 (2:230050331 C>T), RS1000968280 (2:230065623 A>G), RS1000993337 (2:230068461 TG>T), RS1001036756 (2:230054896 G>A), RS1001148420 (2:230037458 T>A,C), RS1001175390 (2:230062155 T>C), RS1001240908 (2:230058231 A>T), RS1001317680 (2:230052268 A>G), RS1001329027 (2:230052136 C>T), RS1001483707 (2:230044382 G>A)

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

1 associations (top):

StudyTraitp-value
GCST005860_3Cholangiocarcinoma in primary sclerosing cholangitis (time to event)1.000000e-06

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

GtoPdb / IUPHAR curated pharmacology

(IUPHAR/BPS Guide to Pharmacology — expert-curated)

Target class: transporter — SLC16 family of monocarboxylate transporters

CTD chemical–gene interactions

58 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, decreases expression, increases expression5
Air Pollutantsaffects expression, increases abundance, decreases expression4
Particulate Matterdecreases expression, increases abundance, affects cotreatment, increases expression4
trichostatin Adecreases expression, increases expression, affects cotreatment3
sodium arseniteincreases expression, decreases expression, affects cotreatment, increases abundance3
Ethanolincreases expression, affects cotreatment, decreases expression, increases abundance3
Tobacco Smoke Pollutionincreases expression, decreases expression3
entinostatdecreases expression, affects cotreatment2
belinostataffects cotreatment, decreases expression2
Panobinostataffects cotreatment, decreases expression2
Arsenicaffects methylation, affects cotreatment, increases abundance, increases expression2
Estradioldecreases expression, increases expression, affects cotreatment2
methylmercuric chlorideincreases expression1
bisphenol Aincreases expression1
2,5,2’,5’-tetrachlorobiphenylincreases expression1
sulforaphaneincreases expression1
manganese chlorideincreases abundance, increases expression, affects cotreatment1
potassium chromate(VI)decreases expression1
cupric chloridedecreases expression1
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression1
CGP 52608affects binding, increases reaction1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
ICG 001increases expression1
dorsomorphinaffects cotreatment, decreases expression1
NSC 689534decreases expression, affects binding1
(+)-JQ1 compounddecreases expression1
4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acidincreases expression1
Temozolomidedecreases expression1
Sunitinibdecreases expression1
Zoledronic Aciddecreases expression1

Cellosaurus cell lines

7 cell lines: 5 cancer cell line, 2 transformed cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_D4DRHEK-SLC16A14-KO-c2Transformed cell lineFemale
CVCL_D4DSHEK-SLC16A14-KO-c6Transformed cell lineFemale
CVCL_D4I3HCT116-SLC16A14-KO-c4Cancer cell lineMale
CVCL_D4I4HCT116-SLC16A14-KO-c5Cancer cell lineMale
CVCL_D4VALS180-SLC16A14-KO-c1Cancer cell lineFemale
CVCL_D4VBLS180-SLC16A14-KO-c8Cancer cell lineFemale
CVCL_TL66HAP1 SLC16A14 (-)Cancer cell lineMale

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): cholangiocarcinoma