DOK1
Docking protein 1
Also known as: DOK1_HUMAN, p62dok
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99704
- Gene
- DOK1
- Ensembl
- ENSG00000115325
- Chromosome
- 2
- Canonical length
- 481 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
The protein encoded by this gene is part of a signal transduction pathway downstream of receptor tyrosine kinases. The encoded protein is a scaffold protein that helps form a platform for the assembly of multiprotein signaling complexes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
Canonical amino-acid sequenceUniProt
481 residues, UniProt reviewed canonical sequence.
>Q99704|DOK1
1 MDGAVMEGPL FLQSQRFGTK RWRKTWAVLY PASPHGVARL EFFDHKGSSS GGGRGSSRRL
61 DCKVIRLAEC VSVAPVTVET PPEPGATAFR LDTAQRSHLL AADAPSSAAW VQTLCRNAFP
121 KGSWTLAPTD NPPKLSALEM LENSLYSPTW EGSQFWVTVQ RTEAAERCGL HGSYVLRVEA
181 ERLTLLTVGA QSQILEPLLS WPYTLLRRYG RDKVMFSFEA GRRCPSGPGT FTFQTAQGND
241 IFQAVETAIH RQKAQGKAGQ GHDVLRADSH EGEVAEGKLP SPPGPQELLD SPPALYAEPL
301 DSLRIAPCPS QDSLYSDPLD STSAQAGEGV QRKKPLYWDL YEHAQQQLLK AKLTDPKEDP
361 IYDEPEGLAP VPPQGLYDLP REPKDAWWCQ ARVKEEGYEL PYNPATDDYA VPPPRSTKPL
421 LAPKPQGPAF PEPGTATGSG IKSHNSALYS QVQKSGASGS WDCGLSRVGT DKTGVKSEGS
481 TLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DOK1 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)
- 0.53
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- spleen: 19 nTPM
- bone marrow: 13 nTPM
- adipose tissue: 12 nTPM
- lymph node: 12 nTPM
- appendix: 9.6 nTPM
- tonsil: 9.5 nTPM
Single-cell type
- megakaryocytes: 148 nCPM
- platelets: 87 nCPM
- hofbauer cells: 63 nCPM
- megakaryocyte progenitors: 35 nCPM
- microglia: 33 nCPM
- hepatic stellate cells: 32 nCPM
Immune cell
- non-classical monocyte: 60 nTPM
- neutrophil: 53 nTPM
- classical monocyte: 52 nTPM
- intermediate monocyte: 51 nTPM
- myeloid DC: 51 nTPM
- total PBMC: 40 nTPM
Brain region
- medulla oblongata: 12 nTPM
- thalamus: 9.2 nTPM
- spinal cord: 8.9 nTPM
- white matter: 8.2 nTPM
- hypothalamus: 7.9 nTPM
- amygdala: 7.8 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)
- 0.64
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 0.09
- DepMap mean gene effect
- -0.13
- 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
- cell surface receptor signaling pathway
- macrophage colony-stimulating factor signaling pathway
- Ras protein signal transduction
- signal transduction
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DOK1 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 DOK1 as an antibody target. Whether an autoantibody or antibody against DOK1 could matter depends on whether native DOK1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DOK1 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 DOK1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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