Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55351
Gene name Gene Name - the full gene name approved by the HGNC.
Serine/threonine kinase 32B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
STK32B
Synonyms (NCBI Gene) Gene synonyms aliases
HSA250839, STK32, STKG6, YANK2
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a serine-threonine protein kinase. Serine-threonine kinases transfer phosphate molecules to the oxygen atoms of serine and threonine. A genomic deletion affecting this gene has been associated with Ellis-van Creveld syndrome, an autosoma
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1397684 hsa-miR-1231 CLIP-seq
MIRT1397685 hsa-miR-3127-5p CLIP-seq
MIRT1397686 hsa-miR-3164 CLIP-seq
MIRT1397687 hsa-miR-3619-3p CLIP-seq
MIRT1397688 hsa-miR-3671 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0004672 Function Protein kinase activity IEA
GO:0004674 Function Protein serine/threonine kinase activity IBA
GO:0004674 Function Protein serine/threonine kinase activity IEA
GO:0005524 Function ATP binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
621309 14217 ENSG00000152953
Protein
UniProt ID Q9NY57
Protein name Serine/threonine-protein kinase 32B (EC 2.7.11.1) (Yet another novel kinase 2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 23 283 Protein kinase domain Domain
Sequence
Sequence length 414
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Celiac disease Celiac disease N/A N/A GWAS
Long QT Syndrome long qt syndrome N/A N/A ClinVar
Schizophrenia Schizophrenia N/A N/A GWAS
Tremor Essential tremor N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Calcinosis Cutis Associate 24885002
Carcinoma Hepatocellular Associate 35800238
Cleft Lip Associate 20087401
Cleft Palate Associate 20087401
Coronary Artery Disease Associate 21626137
Essential Tremor Associate 27797806, 28801652
Essential Tremor Inhibit 28801652
general anxiety disorder Associate 29604450
Inflammation Associate 24885002
Neoplasm Metastasis Associate 24885002