SLC22A10

gene
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Also known as OAT5hOAT5

Summary

SLC22A10 (solute carrier family 22 member 10 (gene/pseudogene), HGNC:18057) is a protein-coding gene on chromosome 11q12.3, encoding Solute carrier family 22 member 10 (Q63ZE4).

Predicted to enable transmembrane transporter activity. Predicted to be involved in organic anion transport. Predicted to be located in membrane.

Source: NCBI Gene 387775 — RefSeq curated summary.

At a glance

  • GWAS associations: 4
  • Clinical variants (ClinVar): 91 total
  • MANE Select transcript: NM_001039752

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:18057
Approved symbolSLC22A10
Namesolute carrier family 22 member 10 (gene/pseudogene)
Location11q12.3
Locus typegene with protein product
StatusApproved
AliasesOAT5, hOAT5
Ensembl geneENSG00000184999
Ensembl biotypeprotein_coding
OMIM607580
Entrez387775

Gene structure

Transcript identifiers

Ensembl transcripts: 14 — 11 protein_coding, 1 retained_intron, 1 protein_coding_CDS_not_defined, 1 nonsense_mediated_decay

ENST00000332793, ENST00000525620, ENST00000526800, ENST00000532724, ENST00000533483, ENST00000682643, ENST00000861889, ENST00000861890, ENST00000861891, ENST00000861892, ENST00000861893, ENST00000861894, ENST00000861895, ENST00000861896

RefSeq mRNA: 1 — MANE Select: NM_001039752 NM_001039752

CCDS: CCDS41661

Canonical transcript exons

ENST00000332793 — 10 exons

ExonStartEnd
ENSE000013268776330232963302543
ENSE000021494696328990363290567
ENSE000021670606331100763311783
ENSE000034615536329951463299629
ENSE000034726476329892063299043
ENSE000034801776329755963297727
ENSE000035122796329154063291643
ENSE000035386906329730363297457
ENSE000036271896330410863304216
ENSE000036845976330468663304889

Expression profiles

Bgee: expression breadth broad, 67 present calls, max score 87.72.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.1324 / max 66.2833, expressed in 9 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
1147880.05356
1147870.04057
1147860.02716
1147890.01135

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
liverUBERON:000210787.72gold quality
right lobe of liverUBERON:000111485.19gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047380.82silver quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099178.45silver quality
quadriceps femorisUBERON:000137770.35gold quality
cerebellar vermisUBERON:000472067.75gold quality
superior frontal gyrusUBERON:000266163.77gold quality
thymusUBERON:000237063.06silver quality
primary visual cortexUBERON:000243660.33gold quality
Brodmann (1909) area 9UBERON:001354059.31gold quality
dorsolateral prefrontal cortexUBERON:000983458.75gold quality
right frontal lobeUBERON:000281058.51gold quality
anterior cingulate cortexUBERON:000983549.98gold quality
cerebral cortexUBERON:000095649.06gold quality
temporal lobeUBERON:000187146.83gold quality
amygdalaUBERON:000187646.59gold quality
frontal cortexUBERON:000187045.77gold quality
lungUBERON:000204845.05gold quality
lower esophagus muscularis layerUBERON:003583344.20gold quality
lower esophagusUBERON:001347344.19gold quality
upper lobe of left lungUBERON:000895243.92gold quality
sural nerveUBERON:001548843.82gold quality
corpus callosumUBERON:000233643.53silver quality
putamenUBERON:000187443.52gold quality
nucleus accumbensUBERON:000188243.31gold quality
cortex of kidneyUBERON:000122541.16gold quality
placentaUBERON:000198740.81gold quality
brainUBERON:000095540.44gold quality
kidneyUBERON:000211339.97gold quality
esophagogastric junction muscularis propriaUBERON:003584139.83gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.39

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): HNF1A

miRNA regulators (miRDB)

61 targeting SLC22A10, 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-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
HSA-LET-7F-2-3P99.9870.982588
HSA-MIR-1185-1-3P99.9871.042593
HSA-MIR-1185-2-3P99.9871.042593
HSA-MIR-477599.9875.006394
HSA-MIR-548N99.9871.944170
HSA-MIR-548AB99.9571.313488
HSA-MIR-55999.9572.283609
HSA-MIR-548A-5P99.9471.273482
HSA-MIR-548AD-5P99.9471.233502
HSA-MIR-548AE-5P99.9471.233502
HSA-MIR-548AK99.9471.243488
HSA-MIR-548AM-5P99.9471.243488
HSA-MIR-548AP-5P99.9471.143489
HSA-MIR-548AQ-5P99.9471.343426
HSA-MIR-548AR-5P99.9471.283515
HSA-MIR-548AS-5P99.9471.223482
HSA-MIR-548AU-5P99.9471.243488
HSA-MIR-548AY-5P99.9471.233502
HSA-MIR-548B-5P99.9471.233502
HSA-MIR-548BB-5P99.9471.273509
HSA-MIR-548C-5P99.9471.243488
HSA-MIR-548D-5P99.9471.233502
HSA-MIR-548H-5P99.9471.243488
HSA-MIR-548I99.9471.253481
HSA-MIR-548J-5P99.9471.143489
HSA-MIR-548O-5P99.9471.243488
HSA-MIR-548W99.9471.243488
HSA-MIR-548Y99.9471.283514

Literature-anchored findings (GeneRIF, showing 1)

  • Illuminating the function of the orphan transporter, SLC22A10, in humans and other primates. (PMID:38782905)

Cross-species orthologs

50 orthologs

OrganismSymbolGene ID
danio_rerioslc22a4ENSDARG00000005335
danio_reriooatxENSDARG00000019713
danio_reriosi:dkey-166k12.1ENSDARG00000054690
danio_rerioslc22a15ENSDARG00000055445
danio_reriosi:dkey-119m7.4ENSDARG00000071049
danio_reriosi:dkey-119m7.8ENSDARG00000096654
drosophila_melanogasterOrctFBGN0019952
drosophila_melanogasterCG15221FBGN0030331
drosophila_melanogasterBalatFBGN0033778
drosophila_melanogasterCG4630FBGN0033809
drosophila_melanogasterCG5592FBGN0035645
drosophila_melanogasterCG10486FBGN0035647
drosophila_melanogasterSLC22AFBGN0037140
drosophila_melanogasterCG7458FBGN0037144
drosophila_melanogasterCG14691FBGN0037829
drosophila_melanogasterCG14855FBGN0038260
drosophila_melanogasterCG14856FBGN0038261
drosophila_melanogasterCG14857FBGN0038262
drosophila_melanogasterCG12783FBGN0038448
drosophila_melanogasterCG7333FBGN0038715
drosophila_melanogasterCG7342FBGN0038716
drosophila_melanogasterCG17751FBGN0038717
drosophila_melanogasterCG17752FBGN0038718
drosophila_melanogasterCG16727FBGN0038719
drosophila_melanogasterCG6231FBGN0038720
drosophila_melanogasterCG4465FBGN0038750
drosophila_melanogasterCG4462FBGN0038752
drosophila_melanogasterCG4459FBGN0038753
drosophila_melanogasterCG6356FBGN0039178
drosophila_melanogasterCG3690FBGN0040350
drosophila_melanogasterCG31103FBGN0051103
drosophila_melanogasterCG31106FBGN0051106
drosophila_melanogasterCG31272FBGN0051272
drosophila_melanogasterCG33233FBGN0053233
drosophila_melanogasterCG33234FBGN0053234
drosophila_melanogasterOrct2FBGN0086365
drosophila_melanogasterCG42269FBGN0259164
drosophila_melanogasterCG44098FBGN0264907
caenorhabditis_elegansWBGENE00003837
caenorhabditis_elegansoct-1WBGENE00003842
caenorhabditis_elegansWBGENE00003843
caenorhabditis_elegansWBGENE00006220
caenorhabditis_elegansWBGENE00008110
caenorhabditis_elegansWBGENE00011456
caenorhabditis_elegansWBGENE00014127
caenorhabditis_elegansWBGENE00015088
caenorhabditis_elegansWBGENE00017751
caenorhabditis_elegansWBGENE00019408
caenorhabditis_elegansWBGENE00020701
caenorhabditis_elegansWBGENE00044455

Paralogs (22): SLC22A16 (ENSG00000004809), SLC22A17 (ENSG00000092096), SLC22A2 (ENSG00000112499), SLC22A7 (ENSG00000137204), SLC22A23 (ENSG00000137266), SLC22A14 (ENSG00000144671), SLC22A3 (ENSG00000146477), SLC22A8 (ENSG00000149452), SLC22A9 (ENSG00000149742), SVOPL (ENSG00000157703), SLC22A15 (ENSG00000163393), SVOP (ENSG00000166111), SLC22A11 (ENSG00000168065), SLC22A13 (ENSG00000172940), SLC22A1 (ENSG00000175003), SLC22A25 (ENSG00000196600), SLC22A4 (ENSG00000197208), SLC22A5 (ENSG00000197375), SLC22A24 (ENSG00000197658), SLC22A12 (ENSG00000197891), SLC22A6 (ENSG00000197901), SLC22A31 (ENSG00000259803)

Protein

Protein identifiers

Solute carrier family 22 member 10Q63ZE4 (reviewed: Q63ZE4)

Alternative names: Organic anion transporter 5

All UniProt accessions (4): Q63ZE4, A0A804HHY1, E9PIT2, E9PMM0

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Tissue specificity. Detected in fetal and adult liver, and in adult kidney.

Similarity. Belongs to the major facilitator (TC 2.A.1) superfamily. Organic cation transporter (TC 2.A.1.19) family.

Isoforms (2)

UniProt IDNamesCanonical?
Q63ZE4-11yes
Q63ZE4-22

RefSeq proteins (1): NP_001034841* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR005828MFS_sugar_transport-likeFamily
IPR020846MFS_domDomain
IPR036259MFS_trans_sfHomologous_superfamily

Pfam: PF00083

UniProt features (29 total): topological domain 12, transmembrane region 11, splice variant 3, glycosylation site 2, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q63ZE4-F187.530.50

Functional residue map

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

Glycosylation sites (2): 56, 102

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 25 (showing top): GOBP_ORGANIC_ANION_TRANSPORT, GOBP_TRANSMEMBRANE_TRANSPORT, GOMF_TRANSPORTER_ACTIVITY, SRSF9_TARGET_GENES, MIR520D_5P, MIR524_5P, MIR374A_5P, MIR1185_1_3P_MIR1185_2_3P, LET_7F_2_3P, MIR374B_5P, MIR7152_5P, MIR4666B, MIR96_3P, MIR6886_3P, MIR3923

GO Biological Process (2): obsolete organic anion transport (GO:0015711), 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

628 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SLC22A10SLC67A1Q96BI1594
SLC22A10OR2L8Q8NGY9519
SLC22A10MAGEB16A2A368512
SLC22A10SLCO4C1Q6ZQN7508
SLC22A10SLCO1A2P46721490
SLC22A10SLC28A1O00337474
SLC22A10UROC1Q96N76474
SLC22A10SLCO3A1Q9UIG8472
SLC22A10SLC22A23A1A5C7459
SLC22A10SLCO4A1Q96BD0455
SLC22A10SLC2A9Q9NRM0452
SLC22A10FAM187BQ17R55439
SLC22A10SLC22A9Q8IVM8436
SLC22A10SLC7A13Q8TCU3429
SLC22A10SLC22A17Q8WUG5427

IntAct

2 interactions, top by confidence:

ABTypeScore
SLC22A10PGRMC1psi-mi:“MI:0914”(association)0.350

BioGRID (22): SLC22A10 (Positive Genetic), ATP13A1 (Affinity Capture-MS), CANX (Affinity Capture-MS), CLGN (Affinity Capture-MS), CLPTM1 (Affinity Capture-MS), DNAJC16 (Affinity Capture-MS), ERLEC1 (Affinity Capture-MS), ERLIN1 (Affinity Capture-MS), ERLIN2 (Affinity Capture-MS), FADS2 (Affinity Capture-MS), FAM8A1 (Affinity Capture-MS), NGLY1 (Affinity Capture-MS), OS9 (Affinity Capture-MS), PGRMC1 (Affinity Capture-MS), PLD3 (Affinity Capture-MS)

ESM2 similar proteins: A0A3Q2IDB4, A0A8B7HA97, A4ZYQ5, A6NK97, G1SZD9, O35956, O57379, O88909, P22732, P23945, P43427, Q0IHM1, Q2KIV1, Q3ZAV1, Q4U2R8, Q4W8A2, Q4W8A3, Q5R9C4, Q5RC45, Q5RCH6, Q5RET7, Q63ZE4, Q66J52, Q6DFR1, Q6NUB3, Q6NYN7, Q6PXP3, Q6T423, Q70BM6, Q76M72, Q76M99, Q80UJ1, Q863Y9, Q864Z3, Q8CFZ5, Q8HY24, Q8IVM8, Q8MK48, Q8N4F4, Q8R0S9

Diamond homologs: A0A3Q2IDB4, A0A8B7HA97, A6NK97, A6QLW8, B2GV36, G1SZD9, O34691, O35956, O57379, O75751, O88446, O88909, Q1RPP5, Q28ES4, Q2KIV1, Q3YAW7, Q3ZAV1, Q4U2R8, Q4W8A2, Q4W8A3, Q5R540, Q5R9C4, Q5RC45, Q5RCH6, Q5RLM2, Q63ZE4, Q66J52, Q66J54, Q6A4L0, Q6NYN7, Q6T423, Q70BM6, Q76M72, Q76M99, Q80UJ1, Q864Z3, Q8CFZ5, Q8HY24, Q8IVM8, Q8MK48

SIGNOR signaling

1 interactions.

AEffectBMechanism
HNF1A“up-regulates quantity by expression”SLC22A10“transcriptional regulation”

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance82
Likely benign5
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1462 predictions. Top by Δscore:

VariantEffectΔscore
11:63299040:AGAGG:Adonor_loss1.0000
11:63299041:GAG:Gdonor_gain1.0000
11:63299041:GAGGT:Gdonor_loss1.0000
11:63299042:AGG:Adonor_loss1.0000
11:63299043:GGT:Gdonor_loss1.0000
11:63299044:G:GGdonor_gain1.0000
11:63299044:GTG:Gdonor_loss1.0000
11:63299045:TGA:Tdonor_loss1.0000
11:63299046:GAG:Gdonor_loss1.0000
11:63304890:G:GGdonor_gain1.0000
11:63297413:C:Tdonor_gain0.9900
11:63297453:GCCCA:Gdonor_gain0.9900
11:63297458:G:GGdonor_gain0.9900
11:63298914:TATCA:Tacceptor_loss0.9900
11:63298915:ATCAG:Aacceptor_gain0.9900
11:63298916:T:Gacceptor_gain0.9900
11:63298916:TCAGG:Tacceptor_loss0.9900
11:63298917:CAG:Cacceptor_loss0.9900
11:63298918:A:Tacceptor_loss0.9900
11:63298918:AGGT:Aacceptor_gain0.9900
11:63298919:G:GCacceptor_loss0.9900
11:63298919:GGTG:Gacceptor_gain0.9900
11:63299039:TAGAG:Tdonor_gain0.9900
11:63299593:G:GGdonor_gain0.9900
11:63299606:GA:Gdonor_gain0.9900
11:63304876:G:GTdonor_gain0.9900
11:63304886:ATCA:Adonor_gain0.9900
11:63304887:TCA:Tdonor_gain0.9900
11:63297557:A:AGacceptor_gain0.9800
11:63297558:G:GGacceptor_gain0.9800

AlphaMissense

3521 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:63290310:T:AC49S0.979
11:63290311:G:CC49S0.979
11:63290283:T:CF40L0.971
11:63290285:T:AF40L0.971
11:63290285:T:GF40L0.971
11:63290436:T:CF91L0.971
11:63290438:T:AF91L0.971
11:63290438:T:GF91L0.971
11:63290172:T:CF3L0.970
11:63290174:T:AF3L0.970
11:63290174:T:GF3L0.970
11:63302480:A:CS408R0.966
11:63302482:C:AS408R0.966
11:63302482:C:GS408R0.966
11:63290511:T:AC116S0.965
11:63290512:G:CC116S0.965
11:63290211:T:CF16L0.958
11:63290213:T:AF16L0.958
11:63290213:T:GF16L0.958
11:63290310:T:CC49R0.958
11:63290525:G:CW120C0.957
11:63290525:G:TW120C0.957
11:63304204:C:AP461H0.957
11:63291552:T:AC139S0.956
11:63291553:G:CC139S0.956
11:63290427:T:AC88S0.954
11:63290428:G:CC88S0.954
11:63304198:T:CL459P0.954
11:63297621:A:CS242R0.953
11:63297623:T:AS242R0.953

dbSNP variants (sampled 300 via entrez): RS1000017286 (11:63308558 A>C,G), RS1000057603 (11:63321539 C>A), RS1000118883 (11:63341247 C>T), RS1000123727 (11:63303215 T>A), RS1000136072 (11:63333791 C>A,T), RS1000159001 (11:63330362 G>A,C), RS1000162178 (11:63355314 C>T), RS1000209039 (11:63361049 G>T), RS1000237909 (11:63297024 A>G), RS1000269391 (11:63288775 T>A), RS1000337791 (11:63338494 A>C,G), RS1000352987 (11:63351260 A>G), RS1000369402 (11:63308245 T>C), RS1000405428 (11:63318320 G>C), RS1000439069 (11:63343210 G>A)

Disease associations

OMIM: gene MIM:607580 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

4 associations (top):

StudyTraitp-value
GCST009733_211Urinary metabolite levels in chronic kidney disease3.000000e-43
GCST009733_240Urinary metabolite levels in chronic kidney disease4.000000e-53
GCST009733_97Urinary metabolite levels in chronic kidney disease2.000000e-11
GCST010512_8Serum uric acid levels4.000000e-12

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0005116urinary metabolite measurement
EFO:0004761uric acid measurement

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 — Orphan or poorly characterized SLC22 family members

CTD chemical–gene interactions

20 total (human), top 20 by PubMed support.

ChemicalActions (top 5)PubMed papers
perfluorooctane sulfonic aciddecreases expression2
Benzo(a)pyreneincreases expression, decreases expression2
methyleugenoldecreases expression1
bisphenol Aaffects cotreatment, increases methylation1
2-amino-9H-pyrido(2,3-b)indoledecreases expression1
sodium arseniteincreases expression1
perfluorooctanoic aciddecreases expression1
perfluoro-n-nonanoic aciddecreases expression1
Rosiglitazonedecreases expression1
Resveratrolaffects cotreatment, decreases expression1
Fulvestrantaffects cotreatment, increases methylation1
Troglitazonedecreases expression1
Endosulfanaffects cotreatment, decreases expression1
Folic Aciddecreases expression1
Plant Extractsaffects cotreatment, decreases expression1
Silicon Dioxideincreases expression1
Tetrachlorodibenzodioxinaffects cotreatment, decreases expression1
Tobacco Smoke Pollutiondecreases expression1
Aflatoxin B1decreases methylation1
Okadaic Aciddecreases expression1

Cellosaurus cell lines

2 cell lines: 2 cancer cell line

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

CellosaurusNameCategorySex
CVCL_D4S6HuH7-SLC22A10-KO-c10Cancer cell lineMale
CVCL_D4S7HuH7-SLC22A10-KO-c15Cancer cell lineMale

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.