STK39 (serine/threonine kinase 39)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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27347 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Serine/threonine kinase 39 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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STK39 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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DCHT, PASK, SPAK |
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Chromosome
Chromosome number
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2 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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2q24.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a serine/threonine kinase that is thought to function in the cellular stress response pathway. The kinase is activated in response to hypotonic stress, leading to phosphorylation of several cation-chloride-coupled cotransporters. The cat |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | ||||||||||||||||
| UniProt ID | Q9UEW8 | |||||||||||||||
| Protein name | STE20/SPS1-related proline-alanine-rich protein kinase (Ste-20-related kinase) (EC 2.7.11.1) (DCHT) (Serine/threonine-protein kinase 39) | |||||||||||||||
| Protein function | Effector serine/threonine-protein kinase component of the WNK-SPAK/OSR1 kinase cascade, which is involved in various processes, such as ion transport, response to hypertonic stress and blood pressure (PubMed:16669787, PubMed:18270262, PubMed:213 | |||||||||||||||
| PDB | 7O86 | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Predominantly expressed in brain and pancreas followed by heart, lung, kidney, skeletal muscle, liver, placenta and testis. {ECO:0000269|PubMed:10980603}. | |||||||||||||||
| Sequence |
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| Sequence length | 545 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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