TNIK

Gene Information
 
Gene Symbol
TNIK
 
Aliases
MRT54
 
Entrez Gene ID
 
Gene Name
TRAF2 and NCK interacting kinase
 
Chromosomal Location
3q26.2-q26.31
 
HGNC ID
 
Summary
Wnt signaling plays important roles in carcinogenesis and embryonic development. The protein encoded by this gene is a serine/threonine kinase that functions as an activator of the Wnt signaling pathway. Mutations in this gene are associated with an autosomal recessive form of cognitive disability. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0000165 Biological process MAPK cascade IBA 21873635
GO:0001934 Biological process Positive regulation of protein phosphorylation IMP 22797597
GO:0006468 Biological process Protein phosphorylation IDA 10521462, 15342639, 22797597
GO:0007010 Biological process Cytoskeleton organization IMP 10521462
GO:0007256 Biological process Activation of JNKK activity IDA 15342639
Protein Information
 
Protein Name
TRAF2 and NCK-interacting protein kinase
 
Function
Serine/threonine kinase that acts as an essential activator of the Wnt signaling pathway. Recruited to promoters of Wnt target genes and required to activate their expression. May act by phosphorylating TCF4/TCF7L2. Appears to act upstream of the JUN N-terminal pathway. May play a role in the response to environmental stress. Part of a signaling complex composed of NEDD4, RAP2A and TNIK which regulates neuronal dendrite extension and arborization during development. More generally, it may play a role in cytoskeletal rearrangements and regulate cell spreading. Phosphorylates SMAD1 on Thr-322.
 
Refseq Proteins
 
UniProt
 
PDB
Pathways
 
Reactome
 

 

Oxidative Stress Induced Senescence

Interactions
 
STRING MINT IntAct
ENSP00000239316
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Endocrine System Diseases
PCOS
Immune System Diseases
Juvenile arthritis
Still Disease
Nervous System Diseases
Arsenic Encephalopathy
Psychiatric/Brain disorders
Mental Retardation
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
 
 
 
Rotterdam criteria 
Related 
30 PCOS subject; Chinese 
TNIK was suggested to serve as biomarkers of oocyte or embryo competence in CCs of PCOS patients. 

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