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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SLC10A4
solute carrier family 10 member 4
Chromosome 4 · 4p11
NCBI Gene: 201780Ensembl: ENSG00000145248.7HGNC: HGNC:22980UniProt: Q96EP9
12PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
plasma membraneprotein bindingbile acid:sodium symporter activitytransmembrane transporter activityuterine fibroiddermatological toxicityresponse to radiationmalnutrition
✦AI Summary

SLC10A4 is a member of the solute carrier family 10 that functions as a vesicular protein in cholinergic and monoaminergic neurons rather than a traditional bile acid transporter 1. The protein exhibits a seven transmembrane domain topology and is ubiquitously expressed in human tissues, with highest levels in brain, placenta, and liver 2. SLC10A4 localizes to synaptic vesicles and is particularly abundant in cholinergic neurons of the central nervous system, co-localizing with markers like choline acetyltransferase and vesicular acetylcholine transporter 1. Despite its similarity to bile acid transporters NTCP and ASBT, SLC10A4 shows no significant transport activity for bile acids under normal conditions 3. However, recent evidence suggests it may function as a protease-activated transporter, gaining bile acid transport activity following cleavage by proteases like thrombin 4. SLC10A4 forms homo- and heterodimers with other SLC10 family members, which may regulate its function 5. In disease contexts, SLC10A4 expression is depleted in Alzheimer's disease, correlating with neuronal degeneration severity 6, and knockout mice display altered dopaminergic signaling and sensory processing deficits relevant to neuropsychiatric disorders 7.

Sources cited
1
SLC10A4 is expressed in cholinergic neurons and has seven transmembrane domains
PMID: 18355966
2
Ubiquitous expression with highest levels in brain, placenta, and liver
PMID: 17106928
3
No transport activity for neurotransmitters or bile acids under normal conditions
PMID: 26084360
4
Functions as protease-activated transporter for bile acids
PMID: 23589386
5
Forms homo- and heterodimers with other SLC10 family members
PMID: 31256060
6
Expression depleted in Alzheimer's disease correlating with neuronal degeneration
PMID: 23948907
7
Knockout mice show altered dopamine signaling and sensory processing deficits
PMID: 38160852
Disease Associationsⓘ20
uterine fibroidOpen Targets
0.27Weak
dermatological toxicityOpen Targets
0.25Weak
response to radiationOpen Targets
0.25Weak
malnutritionOpen Targets
0.21Weak
nephritisOpen Targets
0.14Weak
NephropathyOpen Targets
0.14Weak
Uterine leiomyomaOpen Targets
0.13Weak
X-linked non-syndromic intellectual disabilityOpen Targets
0.10Suggestive
Generalized epilepsy with febrile seizures-plusOpen Targets
0.09Suggestive
thrombophiliaOpen Targets
0.08Suggestive
generalised epilepsyOpen Targets
0.08Suggestive
temporal lobe epilepsyOpen Targets
0.08Suggestive
autosomal dominant epilepsy with auditory featuresOpen Targets
0.08Suggestive
familial temporal lobe epilepsy 2Open Targets
0.07Suggestive
juvenile myoclonic epilepsyOpen Targets
0.07Suggestive
15q13.3 microdeletion syndromeOpen Targets
0.07Suggestive
chromosome 15q13.3 microdeletion syndromeOpen Targets
0.07Suggestive
intellectual disability, autosomal dominant 10Open Targets
0.07Suggestive
intellectual disability, autosomal dominant 3Open Targets
0.07Suggestive
Febrile seizure (within the age range of 3 months to 6 years)Open Targets
0.07Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
SLC10A2Shared pathway100%SLC10A6Shared pathway100%SLC10A5Shared pathway71%SLC10A3Shared pathway68%STARD5Shared pathway50%SLC51BShared pathway50%
Tissue Expression6 tissues
Brain
100%
Bone Marrow
84%
Heart
3%
Ovary
2%
Lung
2%
Liver
2%
Gene Interaction Network
Click a node to explore
SLC10A4SLC10A2SLC10A6SLC10A5SLC10A3STARD5SLC51B
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q96EP9
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.18LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.79 [0.54–1.18]
RankingsWhere SLC10A4 stands among ~20K protein-coding genes
  • #16,569of 20,598
    Most Researched12
  • #12,380of 17,882
    Most Constrained (LOEUF)1.18
Genes detectedSLC10A4
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Distribution of SLC10A4, a synaptic vesicle protein in the human brain, and the association of this protein with Alzheimer's disease-related neuronal degeneration.
PMID: 23948907
J Alzheimers Dis · 2013
1.00
2
The solute carrier family 10 (SLC10): beyond bile acid transport.
PMID: 23506869
Mol Aspects Med · 2013
0.90
3
Cloning and expression of SLC10A4, a putative organic anion transport protein.
PMID: 17106928
World J Gastroenterol · 2006
0.80
4
Unraveling the role of Slc10a4 in auditory processing and sensory motor gating: Implications for neuropsychiatric disorders?
PMID: 38160852
Prog Neuropsychopharmacol Biol Psychiatry · 2024
0.70
5
Expression, sorting and transport studies for the orphan carrier SLC10A4 in neuronal and non-neuronal cell lines and in Xenopus laevis oocytes.
PMID: 26084360
BMC Neurosci · 2015
0.60