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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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ODF1
outer dense fiber of sperm tails 1
Chromosome 8 · 8q22.3
NCBI Gene: 4956Ensembl: ENSG00000155087.4HGNC: HGNC:8113UniProt: Q14990
30PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingnucleusmanchettesperm flagellumIGA glomerulonephritischronic lymphocytic leukemiagoutjoint disease
✦AI Summary

ODF1 (outer dense fiber of sperm tails 1) encodes a major structural protein component of the outer dense fibers in mammalian sperm tails, functioning as a small heat shock protein (HSPB10) with molecular chaperone activity 1. The protein is essential for maintaining the rigid junction between sperm head and tail, as demonstrated by targeted deletion studies in mice where Odf1-deficient males showed complete infertility due to sperm head detachment 1. ODF1 also plays a critical role in organizing the mitochondrial sheath and outer dense fiber structure within the sperm tail 1. Clinical significance is evident in human male infertility, where ODF1 expression is significantly decreased in asthenozoospermic men with reduced sperm motility compared to normozoospermic controls 2. Furthermore, ODF1 interacts with SUN5 and Nesprin3 to form a 'triplet' structure at the sperm neck region, and disruption of this complex contributes to acephalic spermatozoa syndrome 3. Even haplo-deficiency of ODF1 can cause subfertility through weakened head-to-tail coupling, suggesting its involvement in unexplained male infertility cases 4. The gene is specifically expressed in spermatids and contains conserved regulatory sequences for testis-specific expression 5.

Sources cited
1
ODF1 is a small heat shock protein essential for sperm head-tail junction and male fertility
PMID: 22037768
2
ODF1 expression is decreased in asthenozoospermic men with reduced sperm motility
PMID: 20112736
3
ODF1 interacts with SUN5 and Nesprin3 to form a triplet structure at sperm neck
PMID: 33848337
4
ODF1 haplo-deficiency causes subfertility through weakened head-to-tail coupling
PMID: 25118300
5
ODF1 is specifically expressed in spermatids with conserved regulatory sequences
PMID: 18562159
Disease Associationsⓘ20
IGA glomerulonephritisOpen Targets
0.32Weak
chronic lymphocytic leukemiaOpen Targets
0.18Weak
goutOpen Targets
0.15Weak
joint diseaseOpen Targets
0.11Weak
azoospermiaOpen Targets
0.11Weak
cervical carcinomaOpen Targets
0.09Suggestive
spermatogenic failure 83Open Targets
0.09Suggestive
spermatogenic failure 58Open Targets
0.09Suggestive
spermatogenic failure 10Open Targets
0.09Suggestive
spermatogenic failure 11Open Targets
0.09Suggestive
spermatogenic failure 79Open Targets
0.09Suggestive
spermatogenic failure 56Open Targets
0.09Suggestive
spermatogenic failure 92Open Targets
0.09Suggestive
spermatogenic failure 94Open Targets
0.09Suggestive
spermatogenic failure 47Open Targets
0.09Suggestive
spermatogenic failure 65Open Targets
0.09Suggestive
spermatogenic failure 84Open Targets
0.09Suggestive
spermatogenic failure 93Open Targets
0.09Suggestive
spermatogenic failure, X-linked, 5Open Targets
0.09Suggestive
spermatogenic failure 40Open Targets
0.09Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
SPAG4Protein interaction100%ODF2Protein interaction90%SPATC1Protein interaction89%AKAP3Protein interaction79%CNTLNProtein interaction78%CCDC42Protein interaction77%
Tissue Expression6 tissues
Brain
100%
Liver
100%
Bone Marrow
50%
Lung
0%
Ovary
0%
Heart
0%
Gene Interaction Network
Click a node to explore
ODF1SPAG4ODF2SPATC1AKAP3CNTLNCCDC42
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q14990
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.72LoF Tolerant
pLIⓘ
0.23Tolerant
Observed/Expected LoF0.42 [0.26–0.72]
RankingsWhere ODF1 stands among ~20K protein-coding genes
  • #11,991of 20,598
    Most Researched30
  • #5,559of 17,882
    Most Constrained (LOEUF)0.72
Genes detectedODF1
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Comparative genomics reveals gene-specific and shared regulatory sequences in the spermatid-expressed mammalian Odf1, Prm1, Prm2, Tnp1, and Tnp2 genes.
PMID: 18562159
Genomics · 2008
1.00
2
Sequence of mouse Odf1 cDNA and its chromosomal localization: extension of the linkage group between human chromosome 8 and mouse chromosome 15.
PMID: 7789171
Cytogenet Cell Genet · 1995
0.90
3
[Differential expression of ODF1 in human ejaculated spermatozoa and its clinical significance].
PMID: 20112736
Zhonghua Nan Ke Xue · 2009
0.80
4
Pathogenesis of acephalic spermatozoa syndrome caused by SUN5 variant.
PMID: 33848337
Mol Hum Reprod · 2021
0.70
5
Haplo-deficiency of ODF1/HSPB10 in mouse sperm causes relaxation of head-to-tail linkage.
PMID: 25118300
Reproduction · 2014
0.60