STK32C (serine/threonine kinase 32C)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 282974 |
| Gene name | Serine/threonine kinase 32C |
| Gene symbol | STK32C |
| Synonyms (NCBI Gene) |
PKEYANK3
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| Chromosome | 10 |
| Chromosome location | 10q26.3 |
| Summary | The protein encoded by this gene is a member of the serine/threonine protein kinase family. It is thought that this family member is functional in brain due to its high expression levels there. DNA methylation differences have been found in this gene in m |
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miRNA
miRNA information provided by mirtarbase database.
18
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q86UX6 | ||||||||||
| Protein name | Serine/threonine-protein kinase 32C (EC 2.7.11.1) (PKE) (Yet another novel kinase 3) | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 486 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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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)
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