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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SEC14L1
SEC14 like lipid binding 1
Chromosome 17 · 17q25.2-q25.3
NCBI Gene: 6397Ensembl: ENSG00000129657.17HGNC: HGNC:10698UniProt: A5PLM6
36PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
Golgi apparatusprotein bindingRIG-I bindingprotein sequestering activityneurodegenerative diseasenervous system diseasecomplicationHerpes Zoster
✦AI Summary

SEC14L1 is a lipid-binding protein that functions primarily as a negative regulator of innate antiviral immunity. It inhibits RIG-I-mediated interferon-β production by binding to the RIG-I caspase activation and recruitment domain (CARD) and competing with MAVS/IPS-1/Cardif for RIG-I interaction, thereby blocking downstream signal propagation 1. The protein contains conserved CRAL/TRIO and PRELI-MSF1 domains required for its inhibitory function 1, and additionally interacts with cholinergic transporters VAChT and CHT1, potentially modulating acetylcholine transport 2. SEC14L1 has significant disease relevance in multiple malignancies. In breast cancer, SEC14L1 overexpression is a strong independent prognostic factor, with protein expression significantly associated with lymphovascular invasion, higher histological grade, HER2 positivity, and shorter survival 3. In prostate cancer, SEC14L1 expression correlates with aggressive features including high Gleason score and early PSA recurrence, particularly in TMPRSS2:ERG-negative tumors 4. SEC14L1 overexpression is also notably frequent in endometrial serous carcinoma 5. A genome-wide haplotype association study identified SEC14L1 variants associated with monoclonal gammopathy of unknown significance, suggesting involvement in innate immunity pathways relevant to multiple myeloma susceptibility 6.

Sources cited
1
SEC14L1 acts as a negative regulator of RIG-I by binding RIG-I-CARD and competing with MAVS for interaction, requiring PRELI-MSF1 and CRAL-TRIO domains
PMID: 23843640
2
SEC14L1 interacts with vesicular acetylcholine transporter (VAChT) and choline transporter (CHT1) through its GOLD domain
PMID: 17092608
3
SEC14L1 protein overexpression is significantly associated with lymphovascular invasion, higher grade, HER2 positivity, and shorter survival in breast cancer
PMID: 29955149
4
SEC14L1 is overexpressed in 80% of prostate cancers; strong expression correlates with high Gleason score, advanced stage, and PSA recurrence in TMPRSS2:ERG-negative tumors
PMID: 25701228
5
SEC14L1 is overexpressed in endometrial serous carcinoma in 75% of cases
PMID: 35283446
6
SEC14L1 haplotypes are associated with monoclonal gammopathy of unknown significance risk through innate immunity pathways
PMID: 39164264
7
SEC14L1 contains CRAL/TRIO domain found in alpha-tocopherol transfer protein and retinal-binding proteins, suggesting lipid transfer function
PMID: 11707779
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.54Moderate
nervous system diseaseOpen Targets
0.33Weak
complicationOpen Targets
0.32Weak
Herpes ZosterOpen Targets
0.32Weak
Alzheimer diseaseOpen Targets
0.31Weak
lysosomal storage diseaseOpen Targets
0.31Weak
multiple sclerosisOpen Targets
0.31Weak
Parkinson diseaseOpen Targets
0.31Weak
alcohol drinkingOpen Targets
0.27Weak
breast diseaseOpen Targets
0.27Weak
ovarian neoplasmOpen Targets
0.26Weak
trigeminal nerve diseaseOpen Targets
0.21Weak
preeclampsiaOpen Targets
0.21Weak
trauma complicationOpen Targets
0.17Weak
hepatitis B virus infectionOpen Targets
0.16Weak
monoclonal B-cell lymphocytosisOpen Targets
0.11Weak
attention deficit hyperactivity disorderOpen Targets
0.05Suggestive
hereditary attention deficit-hyperactivity disorderOpen Targets
0.04Suggestive
type 2 diabetes mellitusOpen Targets
0.04Suggestive
schizophrenia 15Open Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
PTPN9Protein interaction90%SEPTIN9Protein interaction86%SLC35G4Shared pathway33%SLC35F4Shared pathway33%SLC35F3Shared pathway33%SLC35F5Shared pathway33%
Tissue Expression6 tissues
Lung
100%
Brain
91%
Bone Marrow
68%
Heart
48%
Ovary
25%
Liver
17%
Gene Interaction Network
Click a node to explore
SEC14L1PTPN9SEPTIN9SLC35G4SLC35F4SLC35F3SLC35F5
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q59HE8
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.73LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.56 [0.44–0.73]
RankingsWhere SEC14L1 stands among ~20K protein-coding genes
  • #10,859of 20,598
    Most Researched36
  • #5,632of 17,882
    Most Constrained (LOEUF)0.73
Genes detectedSEC14L1
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance.
PMID: 39164264
Blood Cancer J · 2024
1.00
2
Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag.
PMID: 11707779
Mamm Genome · 2001
0.90
3
Evaluation of Saccharomyces cerevisiae -like 1 (SEC14L1) in Gynecologic Malignancies Shows Overexpression in Endometrial Serous Carcinoma.
PMID: 35283446
Int J Gynecol Pathol · 2023
0.80
4
A 12-gene expression signature is associated with aggressive histological in prostate cancer: SEC14L1 and TCEB1 genes are potential markers of progression.
PMID: 23083832
Am J Pathol · 2012
0.70
5
Negative regulation of RIG-I-mediated innate antiviral signaling by SEC14L1.
PMID: 23843640
J Virol · 2013
0.60