Gene Gene information from NCBI Gene database.
Entrez ID 55351
Gene name Serine/threonine kinase 32B
Gene symbol STK32B
Synonyms (NCBI Gene)
HSA250839STK32STKG6YANK2
Chromosome 4
Chromosome location 4p16.2
Summary 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.
66
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621309 14217 ENSG00000152953
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CELIAC DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ESSENTIAL TREMOR GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Familial cancer of breast Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Alzheimer`s Disease Alzheimer disease GWASDB_DG 23535033
★☆☆☆☆
Found in Text Mining only
Alzheimer`s Disease Alzheimer disease GWASCAT_DG 23535033
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 35800238 Associate
★☆☆☆☆
Found in Text Mining only
Cleft Lip Cleft lip Pubtator 20087401 Associate
★☆☆☆☆
Found in Text Mining only
Cleft Lip with or without Cleft Palate Cleft Lip With Or Without Cleft Palate BEFREE 20087401
★☆☆☆☆
Found in Text Mining only
Cleft Palate Cleft palate Pubtator 20087401 Associate
★☆☆☆☆
Found in Text Mining only
Coronary Artery Disease Coronary artery disease Pubtator 21626137 Associate
★☆☆☆☆
Found in Text Mining only
Coronary heart disease Coronary Heart Disease GWASDB_DG 21626137
★☆☆☆☆
Found in Text Mining only
Ellis-Van Creveld Syndrome Ellis-Van Creveld Syndrome BEFREE 18454448
★☆☆☆☆
Found in Text Mining only
Essential Tremor Tremor BEFREE 27797806, 28801652
★★☆☆☆
Found in Text Mining + Unknown/Other Associations