AtlasGene
ODAD1
outer dynein arm docking complex subunit 1
- HGNC 26560↗(opens in a new tab)
- Ensembl gene ENSG00000105479↗(opens in a new tab)
- NCBI Gene 93233↗(opens in a new tab)
Summary
- Cytogenetic location
- 19q13.33
- Coordinates
- Chromosome 19: 48,296,462–48,321,971 (GRCh38)
- Exons
- 16 exons across 25.5 kb
- Protein
- 707 amino acids
- Also known as
- FLJ32926, CILD20
- Previous symbols
- CCDC114
- MANE Select transcript
- ENST00000674294.1NM_001364171.2
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
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Get my Genome TestCurated report relevant to this gene
Primary Ciliary Dyskinesia
- Autosomal recessive
A rare, genetically heterogeneous, primarily respiratory disorder characterized by chronic upper and lower respiratory tract disease. Approximately half of PCD patients have an organ laterality defect (situs inversus totalis or situs ambiguus/heterotaxy).
- ClinGen rates the link definitive
- 3 GenCC submitters rate it definitive or strong
How ODAD1 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 3 kb of the gene's 25.5 kb; 2,124 of those bases code for the protein.
Sequencing ODAD1
6Low
How hard ODAD1 is to sequence with short reads, out of 100Each bar is the share of ODAD1's exon bases in that kind of difficult region. The score weighs them by how much each costs a short-read call: 0 when no base is in any, 100 when every base is in all of them.
- MappabilityStretches where 100 or 250 bp reads cannot be placed uniquely, so a call there may be missing or wrong. Weight 35%.0%
- HomologySegmental duplications: copies elsewhere in the genome, such as paralogues and pseudogenes, at 90% identity or more. Weight 30%.0%
- RepeatsTandem repeats and runs of one base, which reads slip on and may not span. Weight 15%.7.7%
- GC contentWindows under 25% or over 65% G and C, which library preparation covers thinly. Weight 10%.45%
- Reference coverageGaps in the reference assembly nearby, where there is no sequence for reads to align to. Weight 10%.0%
30
positions in ODAD1 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 25.5 kb of ODAD1, introns included, not only the 3 kb of exons.
Genes linked to the same conditions
- CCDC39coiled-coil domain 39 molecular ruler complex subunitShares 1 condition
- CCDC40coiled-coil domain 40 molecular ruler complex subunitShares 1 condition
- CCNOcyclin OShares 1 condition
- CENPFcentromere protein FShares 1 condition
- CFAP20DCCFAP20 domain containingShares 1 condition
- CFAP221cilia and flagella associated protein 221Shares 1 condition
- CFAP298cilia and flagella associated protein 298Shares 1 condition
- CFAP300cilia and flagella associated protein 300Shares 1 condition
- CFAP54cilia and flagella associated protein 54Shares 1 condition
- CLXNcalaxinShares 1 condition
- DAW1dynein assembly factor with WD repeats 1Shares 1 condition
- DNAAF1dynein axonemal assembly factor 1Shares 1 condition
Traits linked to ODAD1
The Human Phenotype Ontology lists these as features of the rare conditions ODAD1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the cardiovascular system
- All organs on wrong side of body
- Abnormal cardiovascular system morphology
- Abnormality of the heart
- Atrial situs inversus
- Double outlet right ventricle
- Heart tip and four chambers point towards right side of body
- Hole in heart wall separating two lower heart chambers
- Increased blood pressure in blood vessels of lungs
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-17: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.17-8666dff2.
Cite this page
Dante Labs. (n.d.). ODAD1 gene: outer dynein arm docking complex subunit 1. Retrieved 18 October 2026, from https://dantelabs.com/genes/odad1
Dante Labs. ODAD1 gene: outer dynein arm docking complex subunit 1 [Internet]. [cited 18 October 2026]. Available from: https://dantelabs.com/genes/odad1
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