SLC10A3

gene
On this page

Also known as P3DXS253E

Summary

SLC10A3 (solute carrier family 10 member 3, HGNC:22979) is a protein-coding gene on chromosome Xq28, encoding P3 protein (P09131). The ubiquitous expression and the conservation of the sequence in distant animal species suggest that the gene codes for a protein with housekeeping functions.

This gene maps to a GC-rich region of the X chromosome and was identified by its proximity to a CpG island. It is thought to be a housekeeping gene. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Source: NCBI Gene 8273 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 73 total
  • MANE Select transcript: NM_019848

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:22979
Approved symbolSLC10A3
Namesolute carrier family 10 member 3
LocationXq28
Locus typegene with protein product
StatusApproved
AliasesP3, DXS253E
Ensembl geneENSG00000126903
Ensembl biotypeprotein_coding
OMIM312090
Entrez8273

Gene structure

Transcript identifiers

Ensembl transcripts: 15 — 15 protein_coding

ENST00000263512, ENST00000369649, ENST00000393586, ENST00000393587, ENST00000453912, ENST00000651600, ENST00000882890, ENST00000882891, ENST00000882892, ENST00000882893, ENST00000882894, ENST00000882895, ENST00000922672, ENST00000922673, ENST00000922674

RefSeq mRNA: 3 — MANE Select: NM_019848 NM_001142391, NM_001142392, NM_019848

CCDS: CCDS14755, CCDS48195

Canonical transcript exons

ENST00000651600 — 2 exons

ExonStartEnd
ENSE00003841872154490307154490629
ENSE00003843615154487311154489082

Expression profiles

Bgee: expression breadth ubiquitous, 229 present calls, max score 91.44.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 39.4910 / max 267.7466, expressed in 1813 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
20103630.77971806
2010378.71131772

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right coronary arteryUBERON:000162591.44gold quality
descending thoracic aortaUBERON:000234591.41gold quality
skin of legUBERON:000151191.38gold quality
thoracic aortaUBERON:000151591.30gold quality
ascending aortaUBERON:000149691.25gold quality
stromal cell of endometriumCL:000225591.13gold quality
right ovaryUBERON:000211891.04gold quality
lower esophagus mucosaUBERON:003583490.60gold quality
aortaUBERON:000094790.52gold quality
granulocyteCL:000009490.42gold quality
deciduaUBERON:000245090.29gold quality
skin of abdomenUBERON:000141690.27gold quality
left ovaryUBERON:000211990.25gold quality
popliteal arteryUBERON:000225090.09gold quality
tibial arteryUBERON:000761090.08gold quality
left coronary arteryUBERON:000162689.78gold quality
left uterine tubeUBERON:000130389.77gold quality
gingival epitheliumUBERON:000194989.70gold quality
apex of heartUBERON:000209889.36gold quality
zone of skinUBERON:000001489.28gold quality
coronary arteryUBERON:000162189.25gold quality
gingivaUBERON:000182889.13gold quality
mucosa of stomachUBERON:000119989.08gold quality
ectocervixUBERON:001224989.05gold quality
esophagus mucosaUBERON:000246988.91gold quality
esophagogastric junction muscularis propriaUBERON:003584188.80gold quality
gall bladderUBERON:000211088.69gold quality
body of uterusUBERON:000985388.60gold quality
esophagusUBERON:000104388.36gold quality
endocervixUBERON:000045888.32gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes5.95

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

38 targeting SLC10A3, 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-6873-3P100.0071.422626
HSA-MIR-9-5P100.0072.282361
HSA-MIR-1277-5P100.0073.955056
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-146A-5P99.9668.93988
HSA-MIR-146B-5P99.9669.13977
HSA-MIR-185-3P99.9567.011743
HSA-MIR-96-5P99.9572.802140
HSA-MIR-7153-5P99.9468.891006
HSA-MIR-1213399.9271.822006
HSA-MIR-1271-5P99.9171.991972
HSA-MIR-454-3P99.9174.011925
HSA-MIR-4671-3P99.8872.461045
HSA-MIR-444799.8567.812900
HSA-MIR-4766-5P99.7569.232662
HSA-MIR-545-5P99.6670.182308
HSA-MIR-129099.5969.902079
HSA-MIR-203A-3P99.4970.562806
HSA-MIR-130A-5P99.3370.262623
HSA-MIR-6878-3P99.2464.23920
HSA-MIR-6744-3P99.2264.41972
HSA-MIR-6797-3P99.1766.94668
HSA-MIR-4757-5P99.1264.51981
HSA-MIR-1909-5P98.9464.01484
HSA-MIR-6846-5P98.8165.861121
HSA-MIR-6848-5P98.8165.491126
HSA-MIR-3135B98.6165.331470
HSA-MIR-607698.6165.69637
HSA-MIR-430398.0168.132304
HSA-MIR-876-5P97.9968.491345

Cross-species orthologs

6 orthologs

OrganismSymbolGene ID
danio_rerioslc10a3ENSDARG00000103220
mus_musculusSlc10a3ENSMUSG00000032806
rattus_norvegicusSlc10a3ENSRNOG00000060580
drosophila_melanogasterCG11655FBGN0030638
drosophila_melanogasterCG9903FBGN0030756
caenorhabditis_elegansWBGENE00044650

Paralogs (5): SLC10A1 (ENSG00000100652), SLC10A2 (ENSG00000125255), SLC10A4 (ENSG00000145248), SLC10A6 (ENSG00000145283), SLC10A5 (ENSG00000253598)

Protein

Protein identifiers

P3 proteinP09131 (reviewed: P09131)

Alternative names: Solute carrier family 10 member 3

All UniProt accessions (3): P09131, A0A0A0MS43, Q5HY78

UniProt curated annotations — full annotation on UniProt →

Function. The ubiquitous expression and the conservation of the sequence in distant animal species suggest that the gene codes for a protein with housekeeping functions.

Subcellular location. Membrane.

Similarity. Belongs to the bile acid:sodium symporter (BASS) (TC 2.A.28) family.

Isoforms (2)

UniProt IDNamesCanonical?
P09131-11yes
P09131-22

RefSeq proteins (3): NP_001135863, NP_001135864, NP_062822* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR002657BilAc:Na_symport/Acr3Family
IPR004710Bilac:Na_transptFamily
IPR038770Na+/solute_symporter_sfHomologous_superfamily
IPR057103NTCP5_P3_NDomain

Pfam: PF01758, PF24690

UniProt features (12 total): transmembrane region 8, chain 1, splice variant 1, sequence variant 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P09131-F177.410.38

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 133 (showing top): CTATGCA_MIR153, MONNIER_POSTRADIATION_TUMOR_ESCAPE_UP, GOBP_ORGANIC_ACID_TRANSPORT, GOBP_ORGANIC_HYDROXY_COMPOUND_TRANSPORT, GOBP_ORGANIC_ANION_TRANSPORT, GOBP_RESPONSE_TO_OXYGEN_CONTAINING_COMPOUND, GOBP_BILE_ACID_AND_BILE_SALT_TRANSPORT, GOBP_RESPONSE_TO_LIPID, GOBP_MONOCARBOXYLIC_ACID_TRANSPORT, GOBP_RESPONSE_TO_RETINOIC_ACID, LIU_CMYB_TARGETS_UP, KIM_WT1_TARGETS_12HR_UP, GOBP_LIPID_LOCALIZATION, MILI_PSEUDOPODIA_CHEMOTAXIS_DN, GOBP_TRANSMEMBRANE_TRANSPORT

GO Biological Process (3): bile acid and bile salt transport (GO:0015721), response to retinoic acid (GO:0032526), transmembrane transport (GO:0055085)

GO Molecular Function (2): bile acid:sodium symporter activity (GO:0008508), symporter activity (GO:0015293)

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

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
lipid transport1
monocarboxylic acid transport1
organic hydroxy compound transport1
response to lipid1
response to oxygen-containing compound1
transport1
cellular process1
organic acid:sodium symporter activity1
bile acid transmembrane transporter activity1
secondary active monocarboxylate transmembrane transporter activity1
secondary active transmembrane transporter activity1
cellular anatomical structure1

Protein interactions and networks

STRING

648 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SLC10A3SLC12A1Q13621776
SLC10A3SLC10A7Q0GE19753
SLC10A3GOLPH3Q9H4A6602
SLC10A3SLC12A2P55011528
SLC10A3VMA12Q8N511477
SLC10A3SLC12A3P55017402
SLC10A3UBL4AP11441369
SLC10A3RTL5Q5HYW3347
SLC10A3TTC16Q8NEE8341
SLC10A3TEX261Q6UWH6338
SLC10A3OCA2Q04671329
SLC10A3SLC35B3Q9H1N7327
SLC10A3FBN1P35555304
SLC10A3SLC10A2Q12908301
SLC10A3SLC10A1Q14973298

IntAct

3 interactions, top by confidence:

ABTypeScore
SORBS1SLC10A3psi-mi:“MI:0915”(physical association)0.370
SLC10A3CPDpsi-mi:“MI:0914”(association)0.350

BioGRID (22): SLC10A3 (Affinity Capture-RNA), SLC10A3 (Affinity Capture-RNA), SLC10A3 (Affinity Capture-RNA), SLC10A3 (Co-fractionation), SLC10A3 (Co-fractionation), SLC10A3 (Co-fractionation), SLC10A3 (Co-fractionation), SLC10A3 (Co-fractionation), SLC10A3 (Co-fractionation), SLC10A3 (Co-fractionation), TVP23B (Co-fractionation), YIPF1 (Co-fractionation), YIPF2 (Co-fractionation), YIPF6 (Co-fractionation), ACTG1 (Affinity Capture-MS)

ESM2 similar proteins: A0AV02, A2AWR3, A2VCW5, A4QN56, A6QP84, B2RXV4, D4A7H1, F7B113, G8XYX6, O08705, O70324, P09131, P19634, P21129, P23791, P26431, P26434, P26435, P36021, P48761, P48762, P97751, Q0V8N6, Q14973, Q28036, Q3KNW5, Q3UEZ8, Q4JLT5, Q5PT54, Q5PT56, Q5R9A7, Q61165, Q70EX6, Q71RS6, Q7Z3F1, Q8BFW9, Q8BLV3, Q8BUE1, Q8BZ00, Q8C261

Diamond homologs: A6QP84, O08705, P09131, P26435, P70172, Q12908, Q14973, Q28727, Q3KNW5, Q3UEZ8, Q4JLT5, Q5PT55, Q5PT56, Q60414, Q62633, Q70EX6, Q7XVB3, Q96EP9, Q9CXB2, B8BDK4, F4JPW1, O34524, P21129, Q1EBV7, Q5PT54, Q5VRB2, Q650U0, Q6K739, Q8RXE8, Q8VYY4, Q8ZKL0, Q93YR2, Q0V8N6

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance41
Likely benign8
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

501 predictions. Top by Δscore:

VariantEffectΔscore
X:154489081:CC:Cacceptor_gain0.9900
X:154489082:CC:Cacceptor_gain0.9900
X:154489083:C:CCacceptor_gain0.9900
X:154489091:G:GCacceptor_gain0.9900
X:154489078:TGTCC:Tacceptor_gain0.9800
X:154489083:C:CAacceptor_loss0.9800
X:154489083:C:Tacceptor_gain0.9800
X:154489084:T:Aacceptor_loss0.9800
X:154489091:G:Cacceptor_gain0.9800
X:154489999:A:Tacceptor_gain0.9800
X:154489080:TCC:Tacceptor_gain0.9700
X:154489081:CCC:Cacceptor_gain0.9700
X:154490301:CCCTA:Cdonor_loss0.9700
X:154490302:CCTA:Cdonor_loss0.9700
X:154490303:CTA:Cdonor_loss0.9700
X:154490304:TA:Tdonor_loss0.9700
X:154490305:A:ATdonor_loss0.9700
X:154490306:CCT:Cdonor_loss0.9700
X:154488947:T:TAdonor_gain0.9600
X:154489998:C:CTacceptor_gain0.9600
X:154489079:GTCC:Gacceptor_gain0.9500
X:154490618:G:Cdonor_gain0.9500
X:154489730:G:Adonor_gain0.9300
X:154490058:C:CTacceptor_gain0.9000
X:154490508:C:Adonor_gain0.9000
X:154489713:CA:Cdonor_gain0.8900
X:154490587:CTCT:Cdonor_loss0.8900
X:154490588:TCTCA:Tdonor_loss0.8900
X:154490589:CTCA:Cdonor_loss0.8900
X:154490590:TCA:Tdonor_loss0.8900

AlphaMissense

3056 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
X:154487864:G:CS359R0.996
X:154487864:G:TS359R0.996
X:154487866:T:GS359R0.996
X:154488119:G:CS274R0.995
X:154488119:G:TS274R0.995
X:154488121:T:GS274R0.995
X:154487687:G:CS418R0.994
X:154487687:G:TS418R0.994
X:154487689:T:GS418R0.994
X:154487943:G:CP333R0.994
X:154487663:G:CS426R0.993
X:154487663:G:TS426R0.993
X:154487665:T:GS426R0.993
X:154487666:G:CN425K0.993
X:154487666:G:TN425K0.993
X:154487691:A:TV417D0.993
X:154488168:A:GL258P0.993
X:154488172:C:GG257R0.993
X:154488318:C:TG208E0.993
X:154488328:A:GC205R0.993
X:154487943:G:TP333H0.992
X:154488171:C:TG257D0.991
X:154487605:A:GS446P0.988
X:154487931:C:TG337D0.988
X:154488707:A:CF78L0.988
X:154488707:A:TF78L0.988
X:154488709:A:GF78L0.988
X:154488157:A:GC262R0.986
X:154488708:A:CF78C0.986
X:154488057:G:TA295D0.985

dbSNP variants (sampled 300 via entrez): RS1000882856 (X:154487666 G>A), RS1001532201 (X:154492412 G>A,T), RS1001759527 (X:154491944 C>T), RS1003194654 (X:154490729 C>T), RS1003245410 (X:154491006 C>T), RS1003433708 (X:154490433 G>A,C), RS1004059292 (X:154490741 C>A), RS1004514309 (X:154491054 T>C), RS1005779722 (X:154489346 G>A), RS1008236188 (X:154491571 T>G), RS1010576976 (X:154490327 G>A), RS1011999814 (X:154491875 C>A,T), RS1015067015 (X:154492503 G>A), RS1016838133 (X:154491068 G>C), RS1017141046 (X:154490748 G>A,C)

Disease associations

OMIM: gene MIM:312090 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

0 associations (top):

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 — SLC10 family of sodium-bile acid co-transporters

CTD chemical–gene interactions

24 total (human), top 24 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneincreases expression, increases methylation2
aristolochic acid Iincreases expression1
sodium arseniteincreases expression1
potassium chromate(VI)decreases expression1
cupric chlorideincreases expression1
di-n-butylphosphoric acidaffects expression1
CGP 52608affects binding, increases reaction1
ICG 001increases expression1
Resveratrolaffects cotreatment, decreases expression1
Sunitinibincreases expression1
Acetaminophenincreases expression1
Diazinonincreases methylation1
Doxorubicindecreases expression1
Estradiolincreases expression1
Plant Extractsaffects cotreatment, decreases expression1
Tobacco Smoke Pollutionincreases expression1
Triclosanincreases expression1
Urethaneincreases expression1
Valproic Acidaffects expression1
Zidovudineincreases expression1
Aflatoxin B1affects expression1
Okadaic Acidincreases expression1
Vitamin K 3affects expression1
Particulate Matterincreases expression1

Cellosaurus cell lines

3 cell lines: 3 cancer cell line

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

CellosaurusNameCategorySex
CVCL_D4HFHCT116-SLC10A3-KO-c2Cancer cell lineMale
CVCL_D4HGHCT116-SLC10A3-KO-c6Cancer cell lineMale
CVCL_TL41HAP1 SLC10A3 (-)Cancer 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.