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8 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SLC22A14
solute carrier family 22 member 14
Chromosome 3 · 3p22.2
NCBI Gene: 9389Ensembl: ENSG00000144671.11HGNC: HGNC:8495UniProt: Q9Y267
21PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingriboflavin transmembrane transporter activitymitochondrial inner membraneplasma membraneneurodegenerative diseaseFollicular Cystdeficiency anemiaazoospermia
✦AI Summary

SLC22A14 is a mitochondrial riboflavin transporter localized to the inner membrane of the spermatozoa midpiece, essential for male fertility 1. The transporter mediates riboflavin uptake, which serves as a precursor for FAD and FMN cofactors critical for oxidative phosphorylation and energy metabolism in sperm 1. SLC22A14-dependent riboflavin transport is required for fatty acid β-oxidation and tricarboxylic acid cycle function, processes vital for spermatozoa motility and ATP generation 1. Loss of functional SLC22A14 causes disrupted flavoenzyme activity, impaired oxidative phosphorylation, and male infertility in mice 1. Clinically, reduced SLC22A14 expression correlates with idiopathic asthenozoospermia (reduced sperm motility) in infertile men 2. Genetic variants in SLC22A14 have been associated with paclitaxel toxicity in lung cancer patients 3 and sorafenib response in hepatocellular carcinoma 4, suggesting pharmacological roles beyond reproduction. The gene was recently deorphaned, transitioning from an uncharacterized transporter to a functionally defined protein with clear physiological importance in sperm bioenergetics 5.

Sources cited
1
SLC22A14 is a mitochondrial riboflavin transporter in spermatozoa required for oxidative phosphorylation, fatty acid β-oxidation, TCA cycle function, and male fertility
PMID: 33882315
2
SLC22A14 expression is significantly reduced in sperm of idiopathic asthenozoospermia patients
PMID: 29726644
3
SLC22A14 was recently deorphaned and confirmed to transport riboflavin with physiological and pharmacological roles requiring further investigation
PMID: 34921098
4
SLC22A14 polymorphisms are associated with sorafenib response in hepatocellular carcinoma patients
PMID: 38396873
5
SLC22A14 variants are associated with paclitaxel toxicity in lung cancer patients
PMID: 30817750
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.40Weak
Follicular CystOpen Targets
0.37Weak
deficiency anemiaOpen Targets
0.33Weak
azoospermiaOpen Targets
0.09Suggestive
spermatogenic failure 65Open Targets
0.06Suggestive
spermatogenic failure, X-linked, 5Open Targets
0.06Suggestive
spermatogenic failure 84Open Targets
0.06Suggestive
spermatogenic failure 93Open Targets
0.06Suggestive
spermatogenic failure 72Open Targets
0.06Suggestive
spermatogenic failure 56Open Targets
0.06Suggestive
spermatogenic failure 92Open Targets
0.06Suggestive
spermatogenic failure 94Open Targets
0.06Suggestive
spermatogenic failure 18Open Targets
0.06Suggestive
spermatogenic failure 27Open Targets
0.06Suggestive
spermatogenic failure 46Open Targets
0.06Suggestive
Abruptio PlacentaeOpen Targets
0.06Suggestive
partial chromosome Y deletionOpen Targets
0.06Suggestive
spermatogenic failure, X-linked, 3Open Targets
0.06Suggestive
spermatogenic failure 43Open Targets
0.06Suggestive
spermatogenic failure 45Open Targets
0.06Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
RTBDNShared pathway100%XYLBProtein interaction96%OXSR1Protein interaction84%SLC52A2Shared pathway50%SLC52A1Shared pathway50%SLC52A3Shared pathway33%
Tissue Expression6 tissues
Bone Marrow
100%
Liver
22%
Lung
16%
Brain
11%
Ovary
9%
Heart
0%
Gene Interaction Network
Click a node to explore
SLC22A14RTBDNXYLBOXSR1SLC52A2SLC52A1SLC52A3
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q9Y267
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.16LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.91 [0.72–1.16]
RankingsWhere SLC22A14 stands among ~20K protein-coding genes
  • #14,013of 20,598
    Most Researched21
  • #12,082of 17,882
    Most Constrained (LOEUF)1.16
Genes detectedSLC22A14
Sources retrieved8 papers
Response time—
📄 Sources
8▼
1
Genetic Biomarkers of Sorafenib Response in Patients with Hepatocellular Carcinoma.
PMID: 38396873
Int J Mol Sci · 2024
1.00
2
PMID: 34921098
Drug Metab Dispos · 2021
0.88
3
SLC22A14 is a mitochondrial riboflavin transporter required for sperm oxidative phosphorylation and male fertility.
PMID: 33882315
Cell Rep · 2021
0.75
4
Alopecia and male infertility in oligotriche mutant mice are caused by a deletion on distal chromosome 9.
PMID: 19002527
Mamm Genome · 2008
0.63
5
[Expressions of SLC22A14 and SPAG6 proteins in the ejaculated sperm of idiopathic asthenozoospermia patients.].
PMID: 29726644
Zhonghua Nan Ke Xue · 2017
0.50