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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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ROPN1L
rhophilin associated tail protein 1 like
Chromosome 5 · 5p15.2
NCBI Gene: 83853Ensembl: ENSG00000145491.13HGNC: HGNC:24060UniProt: Q96C74
21PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
ciliumcytoplasmmotile ciliumprotein bindinginfectionidiopathic pulmonary fibrosisinterstitial lung diseasechronic obstructive pulmonary disease
✦AI Summary

ROPN1L (rhophilin associated tail protein 1 like) functions as a critical component of sperm flagellar radial spoke complexes, specifically forming part of the radial spoke 1 (RS1) stalk structure that regulates sperm motility 1. The protein is essential for male fertility, as concurrent deficiency of ROPN1 and ROPN1L in mice causes structural abnormalities and complete sperm immotility leading to infertility 2. ROPN1L participates in the assembly of RS1 complexes that connect peripheral doublet microtubules to the central pair, forming a structure necessary for proper flagellar beat frequency and amplitude 1. The protein is significantly downregulated in cryptorchid testes, correlating with progressive loss of spermatogenesis and declining fertility with age 3. Beyond reproductive function, ROPN1L has been identified as a potential biomarker in various disease contexts, including decreased expression in idiopathic pulmonary fibrosis 4 and associations with body mass index variations 5. The protein also shows expression in multi-ciliated cells in breast cancer tissues 6 and serves as a blood-based classifier for facioscapulohumeral muscular dystrophy patients 7, suggesting broader roles beyond sperm function.

Sources cited
1
ROPN1L forms part of the radial spoke 1 stalk structure and is critical for sperm motility regulation
PMID: 39849482
2
Concurrent deficiency of ROPN1 and ROPN1L causes sperm structural abnormalities and infertility in mice
PMID: 25124046
3
ROPN1L is significantly downregulated in cryptorchid testes with progressive loss of spermatogenesis
PMID: 38027210
4
ROPN1L shows decreased expression in idiopathic pulmonary fibrosis patients
PMID: 40538010
5
ROPN1L variants are associated with body mass index variations
PMID: 22446040
6
ROPN1L is expressed in multi-ciliated cells in breast cancer tissues
PMID: 39936988
7
ROPN1L serves as a blood-based classifier for facioscapulohumeral muscular dystrophy patients
PMID: 33067535
Disease Associationsⓘ20
infectionOpen Targets
0.11Weak
idiopathic pulmonary fibrosisOpen Targets
0.10Weak
interstitial lung diseaseOpen Targets
0.09Suggestive
chronic obstructive pulmonary diseaseOpen Targets
0.09Suggestive
acute respiratory distress syndromeOpen Targets
0.08Suggestive
non-alcoholic fatty liver diseaseOpen Targets
0.08Suggestive
idiopathic interstitial pneumoniaOpen Targets
0.08Suggestive
cryopyrin-associated periodic syndromeOpen Targets
0.08Suggestive
coronary artery diseaseOpen Targets
0.07Suggestive
pneumoniaOpen Targets
0.07Suggestive
COVID-19Open Targets
0.06Suggestive
asthmaOpen Targets
0.06Suggestive
gastritisOpen Targets
0.06Suggestive
pulmonary fibrosisOpen Targets
0.06Suggestive
hepatocellular carcinomaOpen Targets
0.05Suggestive
colorectal carcinomaOpen Targets
0.05Suggestive
Hypoplastic amelogenesis imperfectaOpen Targets
0.05Suggestive
Hypomaturation amelogenesis imperfectaOpen Targets
0.05Suggestive
cancerOpen Targets
0.05Suggestive
acute kidney injuryOpen Targets
0.05Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
AKAP3Protein interaction94%SPA17Protein interaction94%RHPN1Protein interaction83%CABYRProtein interaction78%RSPH3Protein interaction68%CFAP251Shared pathway50%
Tissue Expression6 tissues
Bone Marrow
100%
Lung
32%
Brain
12%
Heart
10%
Liver
5%
Ovary
3%
Gene Interaction Network
Click a node to explore
ROPN1LAKAP3SPA17RHPN1CABYRRSPH3CFAP251
PROTEIN STRUCTURE
Preparing viewer…
PDB8J07 · 4.10 Å · EM
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
1.40LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.97 [0.69–1.40]
RankingsWhere ROPN1L stands among ~20K protein-coding genes
  • #13,998of 20,598
    Most Researched21
  • #14,468of 17,882
    Most Constrained (LOEUF)1.40
Genes detectedROPN1L
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Opisthorchis viverrini: analysis of the sperm-specific rhophilin associated tail protein 1-like.
PMID: 25124046
Acta Trop · 2014
1.00
2
Machine Learning-Driven Discovery of TRIM Genes as Diagnostic Biomarkers for Idiopathic Pulmonary Fibrosis.
PMID: 40538010
Med Sci Monit · 2025
0.90
3
A novel locus for body mass index on 5p15.2: a meta-analysis of two genome-wide association studies.
PMID: 22446040
Gene · 2012
0.80
4
RNA sequencing profiles reveals progressively reduced spermatogenesis with progression in adult cryptorchidism.
PMID: 38027210
Front Endocrinol (Lausanne) · 2023
0.70
5
IQUB mutation induces radial spoke 1 deficiency causing asthenozoospermia with normal sperm morphology in humans and mice.
PMID: 39849482
Cell Commun Signal · 2025
0.60