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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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FBXL19
F-box and leucine rich repeat protein 19
Chromosome 16 · 16p11.2
NCBI Gene: 54620Ensembl: ENSG00000099364HGNC: HGNC:25300UniProt: H3BPZ0
45PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
unmethylated CpG bindingubiquitin-like ligase-substrate adaptor activityproteasome-mediated ubiquitin-dependent protein catabolic processprotein bindingneurodegenerative diseaseAbnormality of the skeletal systemNeurodevelopmental delaypreeclampsia
✦AI Summary

FBXL19 is a substrate-recognition component of SCF-type E3 ubiquitin ligase complexes that regulates multiple cellular processes through protein degradation and transcriptional control 12. The protein mediates ubiquitination and degradation of key signaling molecules including RHOA in an ERK2-dependent manner 3, and RAC1/RAC3, thereby suppressing TGFB1-induced cell migration 41. Beyond cytoplasmic functions, FBXL19 localizes to the nucleus where it binds unmethylated CpG dinucleotides and recruits CDK-mediator complexes to chr16, facilitating developmental gene activation 5. FBXL19 is associated with psoriasis and psoriatic arthritis susceptibility through genome-wide association studies, implicating roles in innate immune and nuclear factor-κB signaling pathways 67. Recent evidence demonstrates that FBXL19 genetic variants correlate with Streptococcus skin colonization and psoriasis severity, likely through IL-33/IL1RL1 axis regulation 8. Additionally, endothelial FBXL19 overexpression protects cardiac tissue from influenza A infection by enhancing interferon-mediated antiviral responses and reducing cellular senescence 9. The antisense lncRNA FBXL19-AS1 functions as an oncogene in multiple cancers via miRNA-mediated pathways 1011.

Sources cited
1
The protein mediates ubiquitination and degradation of key signaling molecules including RHOA in an ERK2-dependent manner , and RAC1/RAC3, thereby suppressing TGFB1-induced cell migration , .
PMID: 23871831
2
Beyond cytoplasmic functions, FBXL19 localizes to the nucleus where it binds unmethylated CpG dinucleotides and recruits CDK-mediator complexes to chr16, facilitating developmental gene activation .
PMID: 29276034
3
Recent evidence demonstrates that FBXL19 genetic variants correlate with Streptococcus skin colonization and psoriasis severity, likely through IL-33/IL1RL1 axis regulation .
PMID: 38898675
4
Additionally, endothelial FBXL19 overexpression protects cardiac tissue from influenza A infection by enhancing interferon-mediated antiviral responses and reducing cellular senescence .
PMID: 39150394
⚠Limited data available — This gene has 4 indexed publications. Summary and analysis may be incomplete.
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.34Weak
Abnormality of the skeletal systemOpen Targets
0.16Weak
Neurodevelopmental delayOpen Targets
0.12Weak
preeclampsiaOpen Targets
0.10Weak
hepatocellular carcinomaOpen Targets
0.10Suggestive
breast cancerOpen Targets
0.08Suggestive
cervical cancerOpen Targets
0.08Suggestive
osteosarcomaOpen Targets
0.08Suggestive
lung cancerOpen Targets
0.08Suggestive
nasopharyngeal carcinomaOpen Targets
0.07Suggestive
gliomaOpen Targets
0.07Suggestive
neurotic disorderOpen Targets
0.07Suggestive
suicidal ideationOpen Targets
0.07Suggestive
Lewy body dementiaOpen Targets
0.06Suggestive
Blackfan-Diamond anemiaOpen Targets
0.05Suggestive
ThrombocytopeniaOpen Targets
0.05Suggestive
neutrophil immunodeficiency syndromeOpen Targets
0.05Suggestive
X-linked severe congenital neutropeniaOpen Targets
0.05Suggestive
neutropenia, severe congenital, 1, autosomal dominantOpen Targets
0.05Suggestive
pneumoniaOpen Targets
0.05Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
NEDD8Protein interaction99%SKP1Protein interaction99%CUL1Protein interaction99%NACC1Protein interaction78%KDM7AProtein interaction77%FBXL22Shared pathway67%
Tissue Expression6 tissues
Ovary
100%
Brain
100%
Bone Marrow
94%
Lung
62%
Liver
49%
Heart
24%
Gene Interaction Network
Click a node to explore
FBXL19NEDD8SKP1CUL1NACC1KDM7AFBXL22
PROTEIN STRUCTURE
Preparing viewer…
PDB6ASB · 2.85 Å · X-ray
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
0.54Moderately Constrained
pLIⓘ
0.89Intermediate
Observed/Expected LoF0.36 [0.24–0.54]
RankingsWhere FBXL19 stands among ~20K protein-coding genes
  • #9,446of 20,598
    Most Researched45
  • #3,426of 17,882
    Most Constrained (LOEUF)0.54 · top quartile
Genes detectedFBXL19
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
FLVCR1-AS1 and FBXL19-AS1: Two Putative lncRNA Candidates in Multiple Human Cancers.
PMID: 36649030
Noncoding RNA · 2022
1.00
2
Identification and characterization of FBXL19 gene in silico.
PMID: 15547684
Int J Mol Med · 2004
0.90
3
Genetics of psoriatic arthritis.
PMID: 25488777
Best Pract Res Clin Rheumatol · 2014
0.80
4
The pathogenesis and genetics of psoriasis.
PMID: 23369832
Actas Dermosifiliogr · 2014
0.70
5
Significant Correlation Between Cutaneous Abundance of Streptococcus and Psoriasis Severity in Patients with FBXL19 Gene Variants.
PMID: 38898675
Acta Derm Venereol · 2024
0.60