CLNK
Cytokine-dependent hematopoietic cell linker
Also known as: CLNK_HUMAN, MIST
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z7G1
- Gene
- CLNK
- Ensembl
- ENSG00000109684
- Chromosome
- 4
- Canonical length
- 428 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
MIST is a member of the SLP76 family of adaptors (see LCP2, MIM 601603; BLNK, MIM 604515). MIST plays a role in the regulation of immunoreceptor signaling, including PLC-gamma (PLCG1; MIM 172420)-mediated B cell antigen receptor (BCR) signaling and FC-epsilon R1 (see FCER1A, MIM 147140)-mediated mast cell degranulation (Cao et al., 1999 [PubMed 10562326]; Goitsuka et al., 2000, 2001 [PubMed 10744659] [PubMed 11463797]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
428 residues, UniProt reviewed canonical sequence.
>Q7Z7G1|CLNK
1 MNRQGNRKTT KEGSNDLKFQ NFSLPKNRSW PRINSATGQY QRMNKPLLDW ERNFAAVLDG
61 AKGHSDDDYD DPELRMEETW QSIKILPARP IKESEYADTH YFKVAMDTPL PLDTRTSISI
121 GQPTWNTQTR LERVDKPISK DVRSQNIKGD ASVRKNKIPL PPPRPLITLP KKYQPLPPEP
181 ESSRPPLSQR HTFPEVQRMP SQISLRDLSE VLEAEKVPHN QRKPESTHLL ENQNTQEIPL
241 AISSSSFTTS NHSVQNRDHR GGMQPCSPQR CQPPASCSPH ENILPYKYTS WRPPFPKRSD
301 RKDVQHNEWY IGEYSRQAVE EAFMKENKDG SFLVRDCSTK SKEEPYVLAV FYENKVYNVK
361 IRFLERNQQF ALGTGLRGDE KFDSVEDIIE HYKNFPIILI DGKDKTGVHR KQCHLTQPLP
421 LTRHLLPLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLNK 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)
- 0.6
- Highest tissue expression
- 6.1 nTPM
Expression across tissuesHPA
Tissue
- kidney: 6.1 nTPM
- lymph node: 2.5 nTPM
- tonsil: 1.5 nTPM
- spleen: 1.4 nTPM
- pituitary gland: 1.2 nTPM
- epididymis: 1.1 nTPM
Single-cell type
- renal collecting duct intercalated cells: 2,616 nCPM
- respiratory ionocytes: 1,052 nCPM
- salivary ionocytes: 880 nCPM
- somatotrophs: 626 nCPM
- epididymal clear cells: 486 nCPM
- cdc: 313 nCPM
Immune cell
- myeloid DC: 2 nTPM
- NK-cell: 1.6 nTPM
- T-reg: 1.5 nTPM
- memory B-cell: 1 nTPM
- naive B-cell: 0.9 nTPM
- basophil: 0.4 nTPM
Brain region
- cerebellum: 5.9 nTPM
- white matter: 4.9 nTPM
- cerebral cortex: 4.4 nTPM
- hypothalamus: 4.2 nTPM
- pons: 4.2 nTPM
- thalamus: 4.2 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)
- 1.77
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.56
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
- intracellular signal transduction
- mast cell degranulation
- negative regulation of natural killer cell activation
- positive regulation of natural killer cell cytokine production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CLNK 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 CLNK as an antibody target. Whether an autoantibody or antibody against CLNK could matter depends on whether native CLNK is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLNK 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 CLNK as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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