DYNLT3
Dynein light chain Tctex-type 3
Also known as: DYLT3_HUMAN, TCTE1L, TCTEX1L
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P51808
- Gene
- DYNLT3
- Ensembl
- ENSG00000165169
- Chromosome
- X
- Canonical length
- 116 aa
- Protein class
- Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of a subclass of dynein light chains. The encoded protein homodimerizes and forms the light chain component of the cytoplasmic dynein motor protein complex. This protein may be important for binding dynein to specific cargos including the spindle checkpoint protein BUB3. This protein may also function independently of dynein as a transcriptional modulator. Pseudogenes of this gene are found on chromosomes 2 and 20.[provided by RefSeq, Mar 2010]
Canonical amino-acid sequenceUniProt
116 residues, UniProt reviewed canonical sequence.
>P51808|DYNLT3
1 MEEYHRHCDE VGFNAEEAHN IVKECVDGVL GGEDYNHNNI NQWTASIVEQ SLTHLVKLGK
61 AYKYIVTCAV VQKSAYGFHT ASSCFWDTTS DGTCTVRWEN RTMNCIVNVF AIAIVLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DYNLT3 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)
- 0.37
- Highest tissue expression
- 60 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 60 nTPM
- adrenal gland: 57 nTPM
- hypothalamus: 53 nTPM
- cerebral cortex: 53 nTPM
- kidney: 47 nTPM
- blood vessel: 46 nTPM
Single-cell type
- esophageal apical cells: 1000 nCPM
- early spermatids: 819 nCPM
- late spermatids: 606 nCPM
- esophageal suprabasal cells: 477 nCPM
- endometrial glandular cells: 399 nCPM
- late primary spermatocytes: 253 nCPM
Immune cell
- MAIT T-cell: 36 nTPM
- memory CD4 T-cell: 24 nTPM
- memory CD8 T-cell: 23 nTPM
- basophil: 21 nTPM
- naive CD4 T-cell: 21 nTPM
- naive CD8 T-cell: 20 nTPM
Brain region
- hypothalamus: 61 nTPM
- pons: 57 nTPM
- medulla oblongata: 51 nTPM
- midbrain: 48 nTPM
- hippocampal formation: 41 nTPM
- thalamus: 41 nTPM
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)
- 0.72
- gnomAD pLI
- 0.72
- gnomAD missense Z
- 0.12
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell division
- microtubule-based movement
- positive regulation of mitotic cell cycle
- regulation of mitotic cell cycle
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DYNLT3 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 DYNLT3 as an antibody target. Whether an autoantibody or antibody against DYNLT3 could matter depends on whether native DYNLT3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DYNLT3 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 DYNLT3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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