SLC16A9

gene
On this page

Also known as FLJ43803MCT9

Summary

SLC16A9 (solute carrier family 16 member 9, HGNC:23520) is a protein-coding gene on chromosome 10q21.2, encoding Monocarboxylate transporter 9 (Q7RTY1). Extracellular pH-and Na(+)-sensitive low-affinity creatine transporter.

Enables carnitine transmembrane transporter activity and creatine transmembrane transporter activity. Involved in carnitine transmembrane transport; creatine transmembrane transport; and urate metabolic process. Located in plasma membrane.

Source: NCBI Gene 220963 — RefSeq curated summary.

At a glance

  • GWAS associations: 28
  • Clinical variants (ClinVar): 67 total
  • MANE Select transcript: NM_194298

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:23520
Approved symbolSLC16A9
Namesolute carrier family 16 member 9
Location10q21.2
Locus typegene with protein product
StatusApproved
AliasesFLJ43803, MCT9
Ensembl geneENSG00000165449
Ensembl biotypeprotein_coding
OMIM614242
Entrez220963

Gene structure

Transcript identifiers

Ensembl transcripts: 22 — 21 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000395347, ENST00000395348, ENST00000490066, ENST00000881708, ENST00000881709, ENST00000881710, ENST00000881711, ENST00000881712, ENST00000881713, ENST00000881714, ENST00000881715, ENST00000881716, ENST00000881717, ENST00000881718, ENST00000881719, ENST00000936198, ENST00000936199, ENST00000947927, ENST00000947928, ENST00000947929, ENST00000947930, ENST00000947931

RefSeq mRNA: 6 — MANE Select: NM_194298 NM_001323977, NM_001323978, NM_001323979, NM_001323980, NM_001323981, NM_194298

CCDS: CCDS7256

Canonical transcript exons

ENST00000395348 — 6 exons

ExonStartEnd
ENSE000011343785965367559654589
ENSE000013813485967277059672913
ENSE000013913725966422759664322
ENSE000015214275968409659684327
ENSE000015214305970947959709850
ENSE000037199615965076459652950

Expression profiles

Bgee: expression breadth ubiquitous, 196 present calls, max score 99.91.

FANTOM5 (CAGE): breadth broad, TPM avg 1.9814 / max 71.5713, expressed in 645 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
1094681.1593451
1094660.5837315
1094670.162686
1094590.075943

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
kidney epitheliumUBERON:000481999.91gold quality
adrenal tissueUBERON:001830398.34gold quality
left adrenal gland cortexUBERON:003582598.00gold quality
adrenal cortexUBERON:000123597.89gold quality
right adrenal glandUBERON:000123397.79gold quality
right adrenal gland cortexUBERON:003582797.79gold quality
left adrenal glandUBERON:000123497.71gold quality
nasal cavity epitheliumUBERON:000538497.24gold quality
adrenal glandUBERON:000236996.56gold quality
adult organismUBERON:000702394.05gold quality
colonic mucosaUBERON:000031792.59gold quality
mucosa of sigmoid colonUBERON:000499392.11gold quality
ileal mucosaUBERON:000033191.24gold quality
adult mammalian kidneyUBERON:000008291.23gold quality
kidneyUBERON:000211389.81gold quality
gingivaUBERON:000182889.52gold quality
esophagus squamous epitheliumUBERON:000692089.46gold quality
gingival epitheliumUBERON:000194989.15gold quality
ventricular zoneUBERON:000305388.90gold quality
oviduct epitheliumUBERON:000480487.94gold quality
right hemisphere of cerebellumUBERON:001489087.48gold quality
cerebellar hemisphereUBERON:000224587.37gold quality
cerebellar cortexUBERON:000212987.18gold quality
fallopian tubeUBERON:000388987.18gold quality
cerebellumUBERON:000203786.47gold quality
rectumUBERON:000105285.99gold quality
palpebral conjunctivaUBERON:000181285.91gold quality
bronchial epithelial cellCL:000232885.88gold quality
left ovaryUBERON:000211985.38gold quality
right uterine tubeUBERON:000130285.25gold quality

Single-cell (SCXA)

Detected in 5 experiment(s), a significant marker in 3.

ExperimentMarker?Max mean expression
E-GEOD-131882yes2032.79
E-CURD-119yes2014.31
E-ANND-3yes6.08
E-CURD-135no1365.49
E-GEOD-124858no77.97

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

132 targeting SLC16A9, 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-3163100.0077.238605
HSA-MIR-8485100.0077.574731
HSA-MIR-4668-3P100.0068.742635
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-5011-5P100.0083.465820
HSA-MIR-3646100.0073.565283
HSA-MIR-340-5P100.0072.504437
HSA-MIR-4682100.0068.891258
HSA-MIR-5692A100.0074.406850
HSA-MIR-450099.9972.722367
HSA-MIR-186-5P99.9970.833707
HSA-MIR-428299.9975.366408
HSA-MIR-548P99.9872.253784
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-3617-3P99.9867.86918
HSA-MIR-485-3P99.9870.681585
HSA-MIR-539-3P99.9870.741616
HSA-MIR-60799.9773.625593
HSA-MIR-548AN99.9770.912817
HSA-LET-7D-5P99.9671.761632
HSA-MIR-445899.9671.641650
HSA-MIR-302E99.9670.742669
HSA-MIR-6825-5P99.9669.813431

Literature-anchored findings (GeneRIF, showing 7)

  • it has a possible physiological role in urate excretion from human intestinal epithelial cells. (PMID:23990105)
  • Strong association of SLC16A9 gene variation with HBsAg loss was identified in Chronic Hepatitis B patients treated with peginterferon and adefovir. (PMID:24824278)
  • Molecular characterization of the orphan transporter SLC16A9, an extracellular pH- and Na(+)-sensitive creatine transporter. (PMID:31784090)
  • SLC1A1, SLC16A9, and CNTN3 Are Potential Biomarkers for the Occurrence of Colorectal Cancer. (PMID:32566650)
  • Monocarboxylate transporter 9 (MCT9) is down-regulated in renal cell carcinoma. (PMID:33555501)
  • The tissue expression of MCT3, MCT8, and MCT9 genes in women with breast cancer. (PMID:34097251)
  • Molecular characteristic analysis of single-nucleotide polymorphisms in SLC16A9/hMCT9. (PMID:37879602)

Cross-species orthologs

18 orthologs

OrganismSymbolGene ID
danio_rerioslc16a9aENSDARG00000013926
danio_rerioslc16a9bENSDARG00000104687
mus_musculusSlc16a9ENSMUSG00000037762
rattus_norvegicusSlc16a9ENSRNOG00000049063
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), SLC16A14 (ENSG00000163053), SLC16A4 (ENSG00000168679), SLC16A5 (ENSG00000170190), SLC16A11 (ENSG00000174326), SLC16A13 (ENSG00000174327)

Protein

Protein identifiers

Monocarboxylate transporter 9Q7RTY1 (reviewed: Q7RTY1)

Alternative names: Solute carrier family 16 member 9

All UniProt accessions (1): Q7RTY1

UniProt curated annotations — full annotation on UniProt →

Function. Extracellular pH-and Na(+)-sensitive low-affinity creatine transporter. Also functions as a pH-independent carnitine efflux transporter.

Subcellular location. Cell membrane.

Activity regulation. 4-guanidinobutyrate and guanidinoethyl sulfonate inhibit the transport activity.

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

RefSeq proteins (6): NP_001310906, NP_001310907, NP_001310908, NP_001310909, NP_001310910, NP_919274* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR011701MFSFamily
IPR020846MFS_domDomain
IPR030767MCT9Family
IPR036259MFS_trans_sfHomologous_superfamily
IPR050327Proton-linked_MCTFamily

Pfam: PF07690

Catalyzed reactions (Rhea), 2 shown:

  • (R)-carnitine(in) = (R)-carnitine(out) (RHEA:34959)
  • creatine(in) = creatine(out) (RHEA:73043)

UniProt features (18 total): transmembrane region 12, sequence variant 3, topological domain 2, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q7RTY1-F176.700.41

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 137 (showing top): GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_MCMV_INFECTION_DN, GSE45365_NK_CELL_VS_CD8A_DC_MCMV_INFECTION_UP, GOBP_MODIFIED_AMINO_ACID_TRANSPORT, chr10q21, ACEVEDO_LIVER_CANCER_WITH_H3K27ME3_UP, GOBP_AMINO_ACID_BETAINE_TRANSPORT, GOBP_ORGANIC_ACID_TRANSPORT, GOBP_QUATERNARY_AMMONIUM_GROUP_TRANSPORT, GOBP_ORGANIC_ANION_TRANSPORT, GOBP_MONOCARBOXYLIC_ACID_TRANSPORT, GOBP_ORGANIC_CATION_TRANSPORT, GOBP_URATE_METABOLIC_PROCESS, CART1_01, GOBP_PURINE_CONTAINING_COMPOUND_METABOLIC_PROCESS, GRADE_COLON_AND_RECTAL_CANCER_DN

GO Biological Process (5): creatine transmembrane transport (GO:0015881), urate metabolic process (GO:0046415), carnitine transmembrane transport (GO:1902603), carboxylic acid transmembrane transport (GO:1905039), transmembrane transport (GO:0055085)

GO Molecular Function (6): creatine transmembrane transporter activity (GO:0005308), monocarboxylic acid transmembrane transporter activity (GO:0008028), carnitine transmembrane transporter activity (GO:0015226), symporter activity (GO:0015293), protein binding (GO:0005515), 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
transmembrane transport3
monocarboxylic acid transport2
modified amino acid transmembrane transporter activity2
modified amino acid transport1
carboxylic acid transmembrane transport1
small molecule metabolic process1
purine-containing compound metabolic process1
carnitine transport1
carboxylic acid transport1
transport1
cellular process1
monocarboxylic acid transmembrane transporter activity1
creatine transmembrane transport1
carboxylic acid transmembrane transporter activity1
quaternary ammonium group transmembrane transporter activity1
carnitine transmembrane transport1
secondary active transmembrane transporter activity1
binding1
transporter activity1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

784 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SLC16A9SLC22A11Q9NSA0757
SLC16A9SLC17A1Q14916737
SLC16A9SLC2A9Q9NRM0730
SLC16A9SLC22A12Q96S37729
SLC16A9SLC17A3O00476713
SLC16A9CARMIL1Q5VZK9667
SLC16A9PDZK1Q5T2W1667
SLC16A9SLC17A4Q9Y2C5657
SLC16A9INHBCP55103545
SLC16A9SLC22A5O76082544
SLC16A9ABCG2Q9UNQ0536
SLC16A9SLC22A4Q9H015502
SLC16A9SLC22A6Q4U2R8481
SLC16A9SLC23A3Q6PIS1470
SLC16A9A1CFQ9NQ94460

IntAct

12 interactions, top by confidence:

ABTypeScore
EIF4A2SLC16A9psi-mi:“MI:0915”(physical association)0.560
KLC4SLC16A9psi-mi:“MI:0915”(physical association)0.560
SLC16A9MRPL11psi-mi:“MI:0915”(physical association)0.560
SLC16A9EIF4A2psi-mi:“MI:0915”(physical association)0.560
SLC16A9KLC4psi-mi:“MI:0915”(physical association)0.560
MRPL11SLC16A9psi-mi:“MI:0915”(physical association)0.560
SLC16A9PB1psi-mi:“MI:0915”(physical association)0.370
SLC16A9RIOK3psi-mi:“MI:0914”(association)0.350

BioGRID (20): SLC16A9 (Two-hybrid), SLC16A9 (Two-hybrid), SLC16A9 (Two-hybrid), SLC16A9 (Affinity Capture-RNA), SLC16A9 (Affinity Capture-RNA), ARL13B (Affinity Capture-MS), CHCHD3 (Affinity Capture-MS), CLCC1 (Affinity Capture-MS), EPHB2 (Affinity Capture-MS), HECTD1 (Affinity Capture-MS), HIGD1A (Affinity Capture-MS), IFNGR1 (Affinity Capture-MS), MRS2 (Affinity Capture-MS), PTPN2 (Affinity Capture-MS), RIOK3 (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, D4A734, G5E8K6, M0RCI4, O15375, O15427, O35308, O35440, O35910, O60669, O70451, O70461, O95907, P53985, P53986, P53987, P53988, P57787, P57788, Q03064, Q17QR6, Q3MHW6, Q503M4, Q5NC32, Q5R5M4, Q5ZJU0, Q63344, Q6GM59, Q6P2X9, Q6ZSM3, Q7RTY0, Q7RTY1, Q7TM99, Q8BGC3, Q8NCK7, Q90632, A0A2U8U2M7, G8XYX6, O70324, P36021

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance54
Likely benign2
Benign2

Top pathogenic / likely-pathogenic (0)

SpliceAI

2152 predictions. Top by Δscore:

VariantEffectΔscore
10:59672827:A:Cdonor_gain1.0000
10:59684094:A:ACdonor_gain1.0000
10:59684095:C:CCdonor_gain1.0000
10:59684095:CTTG:Cdonor_gain1.0000
10:59664222:TATAC:Tdonor_loss0.9900
10:59664223:ATACC:Adonor_loss0.9900
10:59664224:TA:Tdonor_loss0.9900
10:59664225:A:Cdonor_loss0.9900
10:59664226:C:CAdonor_loss0.9900
10:59664227:C:Adonor_loss0.9900
10:59664321:ACC:Aacceptor_loss0.9900
10:59664323:CT:Cacceptor_loss0.9900
10:59664324:T:Aacceptor_loss0.9900
10:59672911:GACC:Gacceptor_loss0.9900
10:59672912:ACC:Aacceptor_loss0.9900
10:59672914:CT:Cacceptor_loss0.9900
10:59684089:CACTT:Cdonor_loss0.9900
10:59684090:ACTTA:Adonor_loss0.9900
10:59684091:CTTAC:Cdonor_loss0.9900
10:59684092:TTAC:Tdonor_loss0.9900
10:59684093:TACTT:Tdonor_loss0.9900
10:59684094:AC:Adonor_loss0.9900
10:59684095:C:Adonor_loss0.9900
10:59684119:G:Adonor_gain0.9900
10:59684210:C:CTacceptor_gain0.9900
10:59684210:C:Tacceptor_gain0.9900
10:59714390:CTA:Cdonor_gain0.9900
10:59735925:TTTAC:Tdonor_loss0.9900
10:59735926:TTA:Tdonor_loss0.9900
10:59735927:TACCT:Tdonor_loss0.9900

AlphaMissense

3296 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
10:59654582:G:CS148R0.998
10:59654582:G:TS148R0.998
10:59654584:T:GS148R0.998
10:59672822:G:CS96R0.998
10:59672822:G:TS96R0.998
10:59672824:T:GS96R0.998
10:59672855:A:CS85R0.998
10:59672855:A:TS85R0.998
10:59672857:T:GS85R0.998
10:59654589:C:TG146D0.997
10:59664267:A:CF132L0.997
10:59664267:A:TF132L0.997
10:59664269:A:GF132L0.997
10:59684174:A:GW40R0.997
10:59684174:A:TW40R0.997
10:59684209:C:TG28E0.997
10:59653702:C:GG442R0.996
10:59653702:C:TG442R0.996
10:59653809:C:TG406E0.996
10:59653810:C:GG406R0.996
10:59653810:C:TG406R0.996
10:59653960:C:GG356R0.996
10:59654503:C:GG175R0.996
10:59654577:C:TG150D0.996
10:59654578:C:GG150R0.996
10:59672912:A:CS66R0.996
10:59672912:A:TS66R0.996
10:59684096:T:GS66R0.996
10:59684137:G:TA52D0.996
10:59653701:C:TG442E0.995

dbSNP variants (sampled 300 via entrez): RS1000126693 (10:59660772 A>G), RS1000136761 (10:59682920 A>G), RS1000144812 (10:59703609 G>T), RS1000189746 (10:59689853 G>A), RS1000199639 (10:59689653 C>T), RS1000266709 (10:59709642 C>A,G,T), RS1000298269 (10:59651254 G>A), RS1000327246 (10:59650958 A>G), RS1000405245 (10:59695505 A>G), RS1000422252 (10:59672453 A>G), RS1000466590 (10:59683294 C>T), RS1000537060 (10:59688094 C>T), RS1000563039 (10:59679993 T>A), RS1000698017 (10:59701822 T>C), RS1000750236 (10:59701359 A>T)

Disease associations

OMIM: gene MIM:614242 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

28 associations (top):

StudyTraitp-value
GCST000418_1Uric acid levels1.000000e-08
GCST001217_37Metabolic traits3.000000e-14
GCST001791_32Urate levels2.000000e-28
GCST002307_1Systolic blood pressure (alcohol consumption interaction)1.000000e-08
GCST002307_10Systolic blood pressure (alcohol consumption interaction)4.000000e-08
GCST002308_9Mean arterial pressure (alcohol consumption interaction)9.000000e-07
GCST002932_31Manganese levels2.000000e-06
GCST004866_1Alopecia areata6.000000e-06
GCST005648_7Serum metabolite concentrations in chronic kidney disease3.000000e-15
GCST005650_210Serum metabolite ratios in chronic kidney disease3.000000e-12
GCST006249_33Serum metabolite levels1.000000e-14
GCST006631_9Nicotine dependence and major depression (severity of comorbidity)5.000000e-06
GCST007733_43Serum uric acid levels3.000000e-17
GCST008970_2Gout2.000000e-16
GCST008971_128Urate levels2.000000e-66
GCST008972_180Urate levels2.000000e-77
GCST008972_95Urate levels1.000000e-10
GCST009391_1650Metabolite levels6.000000e-07
GCST010242_205HDL cholesterol levels6.000000e-09
GCST010244_162Triglyceride levels2.000000e-11
GCST011436_3Total carotid plaque area (excess vs minimal atherosclerosis)7.000000e-06
GCST012020_411Serum metabolite levels2.000000e-12
GCST012020_412Serum metabolite levels5.000000e-11
GCST012020_413Serum metabolite levels3.000000e-48
GCST012338_25Gout7.000000e-20
GCST90000025_431Appendicular lean mass1.000000e-13
GCST90002384_189Hemoglobin1.000000e-09
GCST90002401_211Platelet distribution width7.000000e-16

EFO canonical traits (15, from GWAS)

EFO IDTrait name
EFO:0004761uric acid measurement
EFO:0004725metabolite measurement
EFO:0004531urate measurement
EFO:0004329alcohol drinking
EFO:0006335systolic blood pressure
EFO:0006340mean arterial pressure
EFO:0007006depressive symptom measurement
EFO:0009262nicotine dependence symptom count
EFO:0010469carnitine measurement
EFO:0004612high density lipoprotein cholesterol measurement
EFO:0004530triglyceride measurement
EFO:0006501carotid plaque build
EFO:0004980appendicular lean mass
EFO:0004509hemoglobin measurement
EFO:0007984platelet component distribution width

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

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

ChemicalActions (top 5)PubMed papers
trichostatin Aaffects cotreatment, decreases expression3
(+)-JQ1 compounddecreases expression3
bisphenol Aaffects cotreatment, increases methylation, increases expression2
Phenylmercuric Acetateaffects cotreatment, decreases expression2
Aflatoxin B1decreases methylation, increases expression2
Cadmium Chloridedecreases expression, increases abundance2
aristolochic acid Idecreases expression1
testosterone undecanoateaffects cotreatment, decreases expression1
mono-(2-ethylhexyl)phthalateincreases expression1
tris(1,3-dichloro-2-propyl)phosphateaffects expression1
sodium arseniteaffects cotreatment, increases abundance, increases expression1
manganese chlorideincreases expression, affects cotreatment, increases abundance1
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression1
beta-methylcholineaffects expression1
avobenzonedecreases expression1
perfluoro-n-nonanoic acidincreases expression1
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
licochalcone Bdecreases expression1
NSC 689534affects binding, decreases expression1
Temozolomideincreases expression1
Sunitinibdecreases expression1
Fulvestrantaffects cotreatment, increases methylation1
Leflunomideincreases expression1
Air Pollutantsincreases abundance, increases expression1
Ethanolincreases expression1
Arsenicaffects cotreatment, increases abundance, increases expression1
Benzo(a)pyreneaffects methylation, increases methylation1
Cadmiumdecreases expression, increases abundance1

Cellosaurus cell lines

5 cell lines: 4 cancer cell line, 1 transformed cell line

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

CellosaurusNameCategorySex
CVCL_D4DTHEK-SLC16A9-KO-c4Transformed cell lineFemale
CVCL_D4IBHCT116-SLC16A9-KO-c10Cancer cell lineMale
CVCL_D4ICHCT116-SLC16A9-KO-c7Cancer cell lineMale
CVCL_TL70HAP1 SLC16A9 (-) 1Cancer cell lineMale
CVCL_XS89HAP1 SLC16A9 (-) 2Cancer 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): alopecia areata, gout