PLK2 (polo like kinase 2)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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10769 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Polo like kinase 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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PLK2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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SNK, hPlk2, hSNK |
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Chromosome
Chromosome number
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5 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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5q11.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a member of the polo family of serine/threonine protein kinases that have a role in normal cell division. This gene is most abundantly expressed in testis, spleen and fetal tissues, and its expression is inducible by se |
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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 | Q9NYY3 | ||||||||||||||||||||
| Protein name | Serine/threonine-protein kinase PLK2 (EC 2.7.11.21) (Polo-like kinase 2) (PLK-2) (hPlk2) (Serine/threonine-protein kinase SNK) (hSNK) (Serum-inducible kinase) | ||||||||||||||||||||
| Protein function | Tumor suppressor serine/threonine-protein kinase involved in synaptic plasticity, centriole duplication and G1/S phase transition. Polo-like kinases act by binding and phosphorylating proteins that are already phosphorylated on a specific motif | ||||||||||||||||||||
| PDB | 4I5M , 4I5P , 4I6B , 4I6F , 4I6H , 4RS6 , 4XB0 | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed at higher level in the fetal lung, kidney, spleen and heart. {ECO:0000269|PubMed:11696980}. | ||||||||||||||||||||
| Sequence |
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| Sequence length | 685 | ||||||||||||||||||||
| 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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