SLC15A5

gene
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Summary

SLC15A5 (solute carrier family 15 member 5, HGNC:33455) is a protein-coding gene on chromosome 12p12.3, encoding Solute carrier family 15 member 5 (A6NIM6). Proton oligopeptide cotransporter.

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

Source: NCBI Gene 729025 — RefSeq curated summary.

At a glance

  • GWAS associations: 5
  • Clinical variants (ClinVar): 102 total
  • MANE Select transcript: NM_001170798

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:33455
Approved symbolSLC15A5
Namesolute carrier family 15 member 5
Location12p12.3
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000188991
Ensembl biotypeprotein_coding
OMIM620324
Entrez729025

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000344941

RefSeq mRNA: 1 — MANE Select: NM_001170798 NM_001170798

Canonical transcript exons

ENST00000344941 — 9 exons

ExonStartEnd
ENSE000013667881619434516194453
ENSE000013725751621689316217024
ENSE000013747761627256116272783
ENSE000013769271625770116257870
ENSE000013776181622441416224602
ENSE000013843691624458016244800
ENSE000013858511618848516189815
ENSE000013912521623968116239867
ENSE000017999511627732516277685

Expression profiles

Bgee: expression breadth broad, 24 present calls, max score 77.04.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047377.04gold quality
cortical plateUBERON:000534346.98gold quality
substantia nigraUBERON:000203845.51gold quality
prefrontal cortexUBERON:000045145.09gold quality
amygdalaUBERON:000187643.86gold quality
temporal lobeUBERON:000187143.66gold quality
hypothalamusUBERON:000189841.93gold quality
Brodmann (1909) area 9UBERON:001354041.18silver quality
caudate nucleusUBERON:000187340.21gold quality
frontal cortexUBERON:000187040.10gold quality
adipose tissueUBERON:000101340.02gold quality
subcutaneous adipose tissueUBERON:000219039.93gold quality
omental fat padUBERON:001041439.72gold quality
sural nerveUBERON:001548839.66gold quality
nucleus accumbensUBERON:000188239.29silver quality
cerebral cortexUBERON:000095638.80gold quality
bone marrow cellCL:000209238.54gold quality
putamenUBERON:000187438.32gold quality
anterior cingulate cortexUBERON:000983538.30silver quality
dorsolateral prefrontal cortexUBERON:000983437.78silver quality
Ammon’s hornUBERON:000195437.77gold quality
brainUBERON:000095537.37gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
liverUBERON:000210736.39gold quality
superior frontal gyrusUBERON:000266135.60gold quality
ganglionic eminenceUBERON:000402335.49gold quality
endometriumUBERON:000129534.74gold quality
granulocyteCL:000009434.46gold quality
right lobe of liverUBERON:000111434.43gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes2.92
E-HCAD-30no35.29

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

87 targeting SLC15A5, 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-200B-3P100.0073.312693
HSA-MIR-200C-3P100.0073.352685
HSA-MIR-429100.0073.442698
HSA-MIR-4455100.0065.481587
HSA-MIR-3924100.0072.092394
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-318599.9968.121959
HSA-MIR-477599.9875.006394
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-LET-7F-2-3P99.9870.982588
HSA-MIR-1185-1-3P99.9871.042593
HSA-MIR-1185-2-3P99.9871.042593
HSA-MIR-3692-3P99.9870.272139
HSA-MIR-590-3P99.9674.346478
HSA-MIR-570-3P99.9672.414910
HSA-MIR-55999.9572.283609
HSA-MIR-548AB99.9571.313488
HSA-MIR-144-3P99.9473.982698
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

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_rerioslc15a5ENSDARG00000089974
mus_musculusSlc15a5ENSMUSG00000044378
rattus_norvegicusSlc15a5ENSRNOG00000007717

Paralogs (4): SLC15A1 (ENSG00000088386), SLC15A3 (ENSG00000110446), SLC15A4 (ENSG00000139370), SLC15A2 (ENSG00000163406)

Protein

Protein identifiers

Solute carrier family 15 member 5A6NIM6 (reviewed: A6NIM6)

All UniProt accessions (1): A6NIM6

UniProt curated annotations — full annotation on UniProt →

Function. Proton oligopeptide cotransporter.

Subcellular location. Membrane.

Similarity. Belongs to the major facilitator superfamily. Proton-dependent oligopeptide transporter (POT/PTR) (TC 2.A.17) family.

RefSeq proteins (1): NP_001164269* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000109POT_famFamily
IPR036259MFS_trans_sfHomologous_superfamily

Pfam: PF00854

UniProt features (16 total): transmembrane region 11, sequence variant 4, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A6NIM6-F176.130.36

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 41 (showing top): GOBP_TRANSMEMBRANE_TRANSPORT, chr12p12, GOMF_ACTIVE_TRANSMEMBRANE_TRANSPORTER_ACTIVITY, GOMF_SECONDARY_ACTIVE_TRANSMEMBRANE_TRANSPORTER_ACTIVITY, GOMF_SYMPORTER_ACTIVITY, GOMF_TRANSPORTER_ACTIVITY, PAX3_TARGET_GENES, MIR153_5P, MIR616_5P, MIR371B_5P, MIR373_5P, GSE10094_LCMV_VS_LISTERIA_IND_EFF_CD4_TCELL_DN, MIR144_3P, MIR12123, MIR6885_3P

GO Biological Process (3): protein transport (GO:0015031), peptide transport (GO:0015833), transmembrane transport (GO:0055085)

GO Molecular Function (3): symporter activity (GO:0015293), transmembrane transporter activity (GO:0022857), protein binding (GO:0005515)

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

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
transport3
intracellular protein localization1
establishment of protein localization1
cellular process1
secondary active transmembrane transporter activity1
transporter activity1
transmembrane transport1
binding1
cellular anatomical structure1

Protein interactions and networks

STRING

854 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SLC15A5SLC13A5Q86YT5953
SLC15A5SLC13A3Q8WWT9734
SLC15A5SLC13A2Q13183730
SLC15A5KLHL36Q8N4N3571
SLC15A5B3KSW5B3KSW5506
SLC15A5PLEKHA5Q9HAU0455
SLC15A5DCLK2Q8N568422
SLC15A5DCDC2BA2VCK2414
SLC15A5DERAQ9Y315408
SLC15A5ACCSLQ4AC99400
SLC15A5MGST1P10620385
SLC15A5SLC25A35Q3KQZ1374
SLC15A5TMEM267Q0VDI3371
SLC15A5MFSD6LQ8IWD5370
SLC15A5WDR38Q5JTN6363

IntAct

263 interactions, top by confidence:

ABTypeScore
SLC15A5SCRIBpsi-mi:“MI:0915”(physical association)0.780
SCRIBSLC15A5psi-mi:“MI:0407”(direct interaction)0.780
SLC15A5SCRIBpsi-mi:“MI:0407”(direct interaction)0.780
PDZK1SLC15A5psi-mi:“MI:0407”(direct interaction)0.620
SLC15A5PDZK1psi-mi:“MI:0407”(direct interaction)0.620
SLC15A5MAGI2psi-mi:“MI:0407”(direct interaction)0.610
MAGI2SLC15A5psi-mi:“MI:0915”(physical association)0.610
PDZRN4SLC15A5psi-mi:“MI:0407”(direct interaction)0.610
PDZRN4SLC15A5psi-mi:“MI:0915”(physical association)0.610
SLC15A5MAST2psi-mi:“MI:0407”(direct interaction)0.610
MAST2SLC15A5psi-mi:“MI:0915”(physical association)0.610
MAGI2SLC15A5psi-mi:“MI:0407”(direct interaction)0.610
SLC15A5PDZRN4psi-mi:“MI:0407”(direct interaction)0.610
SLC15A5SHANK3psi-mi:“MI:0407”(direct interaction)0.440
SLC15A5MPDZpsi-mi:“MI:0407”(direct interaction)0.440
SNX27SLC15A5psi-mi:“MI:0407”(direct interaction)0.440
SLC15A5SHANK2psi-mi:“MI:0407”(direct interaction)0.440
SLC15A5PDZRN3psi-mi:“MI:0407”(direct interaction)0.440

ESM2 similar proteins: A1Z7R6, A6NIM6, A6QNW6, A9JTG4, A9X4U2, E1BPQ3, F4I9E1, F4KIL8, F5H094, G3V0H7, O35913, O80436, O94911, Q497L8, Q497L9, Q4G0N8, Q4R445, Q5BIZ0, Q5BK75, Q5TAH2, Q5XGZ9, Q68EU6, Q6DBX0, Q6TAC4, Q6UJY2, Q7SXB7, Q86UG4, Q8C0X7, Q8CBB2, Q8IUA7, Q8K440, Q8K441, Q8K442, Q8K449, Q8N139, Q8R0C3, Q8R0S9, Q8WWZ4, Q924V4, Q96RN1

Diamond homologs: A6NIM6, Q8CBB2

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 110 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

Reactome pathways:

PathwayPartnersFoldFDR
Ras activation upon Ca2+ influx through NMDA receptor540.8×6e-06
Unblocking of NMDA receptors, glutamate binding and activation538.8×6e-06
Negative regulation of NMDA receptor-mediated neuronal transmission538.8×6e-06
Assembly and cell surface presentation of NMDA receptors1036.2×1e-11
Dopamine Neurotransmitter Release Cycle535.5×8e-06
Long-term potentiation534.0×9e-06
Neurexins and neuroligins1233.8×2e-13
Protein-protein interactions at synapses830.4×1e-08

GO biological processes:

GO termPartnersFoldFDR
establishment or maintenance of epithelial cell apical/basal polarity1267.7×4e-17
protein localization to synapse752.1×9e-09
receptor clustering848.5×9e-10
regulation of postsynaptic membrane neurotransmitter receptor levels733.7×2e-07
social behavior513.2×1e-03
Rho protein signal transduction512.0×1e-03
protein-containing complex assembly1011.1×3e-06
cell-cell adhesion109.9×6e-06

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance89
Likely benign6
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1624 predictions. Top by Δscore:

VariantEffectΔscore
12:16189812:ATATC:Aacceptor_loss0.9900
12:16189813:TAT:Tacceptor_gain0.9900
12:16189814:ATCTA:Aacceptor_loss0.9900
12:16189815:TCT:Tacceptor_loss0.9900
12:16189816:C:CCacceptor_gain0.9900
12:16189816:CT:Cacceptor_loss0.9900
12:16224413:CGGG:Cdonor_gain0.9900
12:16224456:A:ACdonor_gain0.9900
12:16224457:C:CCdonor_gain0.9900
12:16224505:T:Adonor_gain0.9900
12:16224603:C:CCacceptor_gain0.9900
12:16239672:TGTAC:Tdonor_loss0.9900
12:16239673:GTAC:Gdonor_loss0.9900
12:16239674:TACT:Tdonor_loss0.9900
12:16239675:ACT:Adonor_loss0.9900
12:16239676:CTTAC:Cdonor_loss0.9900
12:16239677:TTA:Tdonor_loss0.9900
12:16239678:TACT:Tdonor_loss0.9900
12:16239679:A:ACdonor_gain0.9900
12:16239679:ACTGA:Adonor_loss0.9900
12:16239680:C:CTdonor_gain0.9900
12:16239680:CTG:Cdonor_gain0.9900
12:16239866:ATC:Aacceptor_loss0.9900
12:16239867:TCTG:Tacceptor_loss0.9900
12:16239868:C:CCacceptor_gain0.9900
12:16239868:C:Tacceptor_loss0.9900
12:16239869:T:Cacceptor_loss0.9900
12:16272553:CTACT:Cdonor_loss0.9900
12:16272554:TACTT:Tdonor_loss0.9900
12:16272555:ACTTA:Adonor_loss0.9900

AlphaMissense

3779 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
12:16224542:C:GR408P0.936
12:16194443:A:CF498L0.837
12:16194443:A:TF498L0.837
12:16194445:A:GF498L0.837
12:16224560:C:TG402D0.836
12:16194374:G:CN521K0.802
12:16194374:G:TN521K0.802
12:16239844:T:AQ333H0.796
12:16239844:T:GQ333H0.796
12:16224550:T:AE405D0.793
12:16224550:T:GE405D0.793
12:16224551:T:AE405V0.792
12:16224561:C:GG402R0.787
12:16277485:A:CF67L0.787
12:16277485:A:TF67L0.787
12:16277487:A:GF67L0.787
12:16277428:A:CF86L0.784
12:16277428:A:TF86L0.784
12:16277430:A:GF86L0.784
12:16194448:A:GW497R0.774
12:16194448:A:TW497R0.774
12:16194393:G:TA515E0.763
12:16257831:A:CF208L0.758
12:16257831:A:TF208L0.758
12:16257833:A:GF208L0.758
12:16224563:G:TA401D0.746
12:16194444:A:GF498S0.740
12:16224597:C:GG390R0.740
12:16224597:C:TG390R0.740
12:16194362:G:CF525L0.738

dbSNP variants (sampled 300 via entrez): RS1000005312 (12:16199491 T>C), RS1000006850 (12:16259346 C>A,G,T), RS1000008817 (12:16218353 T>A), RS1000047058 (12:16237224 G>A,C), RS1000101822 (12:16252972 C>G), RS1000108359 (12:16276007 A>G), RS1000161243 (12:16204907 T>G), RS1000177352 (12:16245615 G>T), RS1000233276 (12:16212587 T>C), RS1000237459 (12:16253245 A>G), RS1000251388 (12:16251613 T>C), RS1000289362 (12:16224435 C>A), RS1000296204 (12:16206427 C>G,T), RS1000364927 (12:16241652 A>G), RS1000408803 (12:16269421 C>G)

Disease associations

OMIM: gene MIM:620324 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

5 associations (top):

StudyTraitp-value
GCST007326_76Number of sexual partners4.000000e-08
GCST007576_214Chronotype3.000000e-08
GCST007940_1Medication use (antidepressants)5.000000e-09
GCST010988_487Adult body size3.000000e-08
GCST90026416_16Mild age-related type 2 diabetes8.000000e-06

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0008328chronotype measurement
EFO:0009940Antidepressant use measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

3 total (human), top 3 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arseniteincreases expression1
Benzo(a)pyreneaffects methylation1
Chlordeconeaffects response to substance1

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.