DOK5
Docking protein 5
Also known as: C20orf180, dJ805C22.1, DOK5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P104
- Gene
- DOK5
- Ensembl
- ENSG00000101134
- Chromosome
- 20
- Canonical length
- 306 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Focal adhesion sites
OverviewNCBI Gene
The protein encoded by this gene is a member of the DOK family of membrane proteins, which are adapter proteins involved in signal transduction. The encoded protein interacts with phosphorylated receptor tyrosine kinases to mediate neurite outgrowth and activation of the MAP kinase pathway. Unlike other DOK family proteins, this protein does not interact with RASGAP. This protein is up-regulated in patients with systemic sclerosis and is associated with fibrosis induced by insulin-like growth factor binding protein 5. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2014]
Canonical amino-acid sequenceUniProt
306 residues, UniProt reviewed canonical sequence.
>Q9P104|DOK5
1 MASNFNDIVK QGYVRIRSRR LGIYQRCWLV FKKASSKGPK RLEKFSDERA AYFRCYHKVT
61 ELNNVKNVAR LPKSTKKHAI GIYFNDDTSK TFACESDLEA DEWCKVLQME CVGTRINDIS
121 LGEPDLLATG VEREQSERFN VYLMPSPNLD VHGECALQIT YEYICLWDVQ NPRVKLISWP
181 LSALRRYGRD TTWFTFEAGR MCETGEGLFI FQTRDGEAIY QKVHSAALAI AEQHERLLQS
241 VKNSMLQMKM SERAASLSTM VPLPRSAYWQ HITRQHSTGQ LYRLQDVSSP LKLHRTETFP
301 AYRSEHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DOK5 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)
- 0.4
- Highest tissue expression
- 43 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 43 nTPM
- tongue: 23 nTPM
- heart muscle: 17 nTPM
- amygdala: 16 nTPM
- cerebral cortex: 15 nTPM
- hypothalamus: 13 nTPM
Single-cell type
- retinal amacrine cells: 366 nCPM
- ependymal cells: 175 nCPM
- myonuclei: 175 nCPM
- müller glia: 148 nCPM
- astrocytes: 147 nCPM
- choroid plexus epithelial cells: 123 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- pons: 24 nTPM
- hypothalamus: 20 nTPM
- medulla oblongata: 18 nTPM
- thalamus: 17 nTPM
- hippocampal formation: 17 nTPM
- midbrain: 15 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)
- 0.83
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.92
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
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 surface receptor protein tyrosine kinase signaling pathway
- neuron differentiation
- positive regulation of MAPK cascade
- regulation of neurotrophin TRK receptor signaling pathway
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DOK5 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 DOK5 as an antibody target. Whether an autoantibody or antibody against DOK5 could matter depends on whether native DOK5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DOK5 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 DOK5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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