Gene Gene information from NCBI Gene database.
Entrez ID 116449
Gene name Cytokine dependent hematopoietic cell linker
Gene symbol CLNK
Synonyms (NCBI Gene)
MIST
Chromosome 4
Chromosome location 4p16.1
Summary 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-eps
miRNA miRNA information provided by mirtarbase database.
131
miRTarBase ID miRNA Experiments Reference
MIRT650701 hsa-miR-548ac HITS-CLIP 23824327
MIRT650700 hsa-miR-548bb-3p HITS-CLIP 23824327
MIRT650699 hsa-miR-548d-3p HITS-CLIP 23824327
MIRT650698 hsa-miR-548h-3p HITS-CLIP 23824327
MIRT650697 hsa-miR-548z HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0002729 Process Positive regulation of natural killer cell cytokine production IEA
GO:0005515 Function Protein binding IPI 16273093, 26009488
GO:0005737 Component Cytoplasm IEA
GO:0005737 Component Cytoplasm IMP 26009488
GO:0007169 Process Cell surface receptor protein tyrosine kinase signaling pathway IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611434 17438 ENSG00000109684
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q7Z7G1
Protein name Cytokine-dependent hematopoietic cell linker (Mast cell immunoreceptor signal transducer)
Protein function An adapter protein which plays a role in the regulation of immunoreceptor signaling, including PLC-gamma-mediated B-cell antigen receptor (BCR) signaling and FC-epsilon R1-mediated mast cell degranulation (By similarity). Together with FGR, it a
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00017 SH2 309 392 SH2 domain Domain
Sequence
MNRQGNRKTTKEGSNDLKFQNFSLPKNRSWPRINSATGQYQRMNKPLLDWERNFAAVLDG
AKGHSDDDYDDPELRMEETWQSIKILPARPIKESEYADTHYFKVAMDTPLPLDTRTSISI
GQPTWNTQTRLERVDKPISKDVRSQNIKGDASVRKNKIPLPPPRPLITLPKKYQPLPPEP
ESSRPPLSQRHTFPEVQRMPSQISLRDLSEVLEAEKVPHNQRKPESTHLLENQNTQEIPL
AISSSSFTTSNHSVQNRDHRGGMQPCSPQRCQPPASCSPHENILPYKYTSWRPPFPKRSD
RKDVQHNEWYIGEYSRQAVEEAFMKENKDGSFLVRDCSTKSKEEPYVLAVFYENKVYNVK
IRFLERNQQFALGTGLRGDEKFDSVEDIIEHY
KNFPIILIDGKDKTGVHRKQCHLTQPLP
LTRHLLPL
Sequence length 428
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
15
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
AUTOIMMUNE THYROID DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CLNK-related disorder Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ESOPHAGEAL DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ESOPHAGEAL ULCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Arthritis, Gouty Gouty arthritis GWASDB_DG 20884846, 23263486
★☆☆☆☆
Found in Text Mining only
Cirrhosis Cirrhosis BEFREE 21756847
★☆☆☆☆
Found in Text Mining only
Foramen Ovale, Patent Patent foramen ovale BEFREE 28283958
★☆☆☆☆
Found in Text Mining only
Gout Gout GWASDB_DG 20884846, 23263486
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Liver Cirrhosis Liver Cirrhosis BEFREE 21756847
★☆☆☆☆
Found in Text Mining only
Ostium secundum atrial septal defect Secundum atrial septal defect BEFREE 28283958
★☆☆☆☆
Found in Text Mining only
Steatohepatitis Fatty Liver BEFREE 24776764
★☆☆☆☆
Found in Text Mining only
Vitiligo Vitiligo CTD_human_DG 22561518
★★☆☆☆
Found in Text Mining + Unknown/Other Associations