DNAL4
Dynein axonemal light chain 4
Also known as: dJ327J16, DNAL4_HUMAN, PIG27
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O96015
- Gene
- DNAL4
- Ensembl
- ENSG00000100246
- Chromosome
- 22
- Canonical length
- 105 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Primary cilium transition zone,Centrosome,Basal body,Cytosol,Acrosome,Equatorial segment,Perinuclear theca,Calyx,Principal piece
OverviewNCBI Gene
This gene encodes an axonemal dynein light chain which functions as a component of the outer dynein arms complex. This complex acts as the molecular motor that provides the force to move cilia in an ATP-dependent manner. The encoded protein is expressed in tissues with motile cilia or flagella and may be involved in the movement of sperm flagella. [provided by RefSeq, Dec 2014]
Canonical amino-acid sequenceUniProt
105 residues, UniProt reviewed canonical sequence.
>O96015|DNAL4
1 MGETEGKKDE ADYKRLQTFP LVRHSDMPEE MRVETMELCV TACEKFSNNN ESAAKMIKET
61 MDKKFGSSWH VVIGEGFGFE ITHEVKNLLY LYFGGTLAVC VWKCSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DNAL4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.35
- Highest tissue expression
- 64 nTPM
Expression across tissuesHPA
Tissue
- testis: 64 nTPM
- amygdala: 37 nTPM
- cerebral cortex: 35 nTPM
- basal ganglia: 34 nTPM
- fallopian tube: 33 nTPM
- hippocampal formation: 31 nTPM
Single-cell type
- late spermatids: 246 nCPM
- early spermatids: 35 nCPM
- late primary spermatocytes: 6.5 nCPM
- platelets: 4.2 nCPM
- fallopian tube ciliated cells: 3 nCPM
- endometrial ciliated cells: 1.9 nCPM
Immune cell
- NK-cell: 16 nTPM
- neutrophil: 15 nTPM
- basophil: 15 nTPM
- MAIT T-cell: 14 nTPM
- plasmacytoid DC: 13 nTPM
- eosinophil: 12 nTPM
Brain region
- basal ganglia: 36 nTPM
- cerebral cortex: 34 nTPM
- hippocampal formation: 30 nTPM
- amygdala: 30 nTPM
- hypothalamus: 29 nTPM
- thalamus: 22 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DNAL4.
Disease | AllUniProt
Conditions DNAL4 is implicated in, by any mechanism.
- Mirror movements 3 (MRMV3) MIM:616059
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 19 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Mirror movements 3
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.7
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.45
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DNAL4 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DNAL4 as an antibody target. Whether an autoantibody or antibody against DNAL4 could matter depends on whether native DNAL4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DNAL4 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label DNAL4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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