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GeneE
2 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
β“˜GeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
CWF19L2
CWF19 like cell cycle control factor 2
Chromosome 11 Β· 11q22.3
NCBI Gene: 143884Ensembl: ENSG00000152404.17HGNC: HGNC:26508UniProt: Q2TBE0
45PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
protein bindingmRNA splicing, via spliceosomepost-mRNA release spliceosomal complexnucleoplasmnephrotic syndromeeye diseasesmoking initiationmetabolic disease
✦AI Summary

Based on limited published evidence, CWF19L2 is a nucleoplasmic protein involved in mRNA splicing and post-mRNA release spliceosomal processes. CWF19L2 functions as a critical component of the intron lariat spliceosome, where it interacts with splicing machinery including DBR1, NVL2, and the RNA exosome complex 1. The protein is required for debranching of intron-derived lariat RNAs, facilitating their nuclear clearance 1. Genomic studies suggest CWF19L2 involvement in cell cycle regulation 2. The protein shares C-terminal homology with yeast Cwf19 and mammalian CWF19L1 1.

Sources cited
1
CWF19L2 interacts with NVL2, DBR1, and RNA exosome components; is required for debranching of intron lariat RNAs; loads into late-stage spliceosome
PMID: 41422678
2
CWF19L2 encodes a protein involved in cell cycle regulation based on genomic association analysis
PMID: 18398821
⚠Limited data available β€” This gene has 2 indexed publications. Summary and analysis may be incomplete.
Disease Associationsβ“˜20
nephrotic syndromeOpen Targets
0.31Weak
eye diseaseOpen Targets
0.29Weak
smoking initiationOpen Targets
0.29Weak
metabolic diseaseOpen Targets
0.26Weak
hypertensionOpen Targets
0.25Weak
essential hypertensionOpen Targets
0.23Weak
chronic obstructive pulmonary diseaseOpen Targets
0.19Weak
coronary atherosclerosisOpen Targets
0.15Weak
Increased blood pressureOpen Targets
0.10Suggestive
cardiovascular diseaseOpen Targets
0.10Suggestive
coronary artery diseaseOpen Targets
0.09Suggestive
response to xenobiotic stimulusOpen Targets
0.06Suggestive
liver diseaseOpen Targets
0.03Suggestive
ankylosing spondylitisOpen Targets
0.02Suggestive
preeclampsiaOpen Targets
0.02Suggestive
cervical carcinomaOpen Targets
0.02Suggestive
ovarian neoplasmOpen Targets
0.02Suggestive
insomniaOpen Targets
0.02Suggestive
male infertilityOpen Targets
0.01Suggestive
breast cancerOpen Targets
0.01Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar β†—
Related Genes
HNRNPA1L3Shared pathway100%RBMXL1Shared pathway100%RBMY1EShared pathway100%RBMY1DShared pathway100%RBM44Shared pathway100%HNRNPA3Shared pathway100%
Tissue Expression6 tissues
Ovary
100%
Brain
96%
Bone Marrow
90%
Heart
64%
Lung
55%
Liver
44%
Gene Interaction Network
Click a node to explore
CWF19L2HNRNPA1L3RBMXL1RBMY1ERBMY1DRBM44HNRNPA3
PROTEIN STRUCTURE
Preparing viewer…
PDB6ID1 Β· 2.86 Γ… Β· EM
View on RCSB β†—
Constraintβ“˜
LOEUFβ“˜
1.03LoF Tolerant
pLIβ“˜
0.00Tolerant
Observed/Expected LoF0.79 [0.61–1.03]
RankingsWhere CWF19L2 stands among ~20K protein-coding genes
  • #9,434of 20,598
    Most Researched45
  • #10,281of 17,882
    Most Constrained (LOEUF)1.03
Genes detectedCWF19L2
Sources retrieved2 papers
Response timeβ€”
πŸ“„ Sources
2
1
Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients.
PMID: 18398821
Genes Chromosomes Cancer Β· 2008
1.00
2
NVL2-interacting protein CWF19L2 is required for debranching of intron-derived lariat RNAs.
PMID: 41422678
Biochem Biophys Res Commun Β· 2026
0.50