Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
139728
Gene name Gene Name - the full gene name approved by the HGNC.
Pregnancy up-regulated nonubiquitous CaM kinase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PNCK
Synonyms (NCBI Gene) Gene synonyms aliases
BSTK3, CaMK1b
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq28
Summary Summary of gene provided in NCBI Entrez Gene.
PNCK is a member of the calcium/calmodulin-dependent protein kinase family of protein serine/threonine kinases (see CAMK1; MIM 604998) (Gardner et al., 2000 [PubMed 10673339]).[supplied by OMIM, Mar 2008]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1244696 hsa-miR-1915 CLIP-seq
MIRT1244697 hsa-miR-2467-3p CLIP-seq
MIRT1244698 hsa-miR-3194-5p CLIP-seq
MIRT1244699 hsa-miR-338-3p CLIP-seq
MIRT1244700 hsa-miR-4323 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004683 Function Calmodulin-dependent protein kinase activity IBA 21873635
GO:0005516 Function Calmodulin binding IBA 21873635
GO:0005524 Function ATP binding IEA
GO:0005622 Component Intracellular anatomical structure IBA 21873635
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300680 13415 ENSG00000130822
Protein
UniProt ID Q6P2M8
Protein name Calcium/calmodulin-dependent protein kinase type 1B (EC 2.7.11.17) (CaM kinase I beta) (CaM kinase IB) (CaM-KI beta) (CaMKI-beta) (Pregnancy up-regulated non-ubiquitously-expressed CaM kinase)
Protein function Calcium/calmodulin-dependent protein kinase belonging to a proposed calcium-triggered signaling cascade. In vitro phosphorylates CREB1 and SYN1/synapsin I. Phosphorylates and activates CAMK1 (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 15 270 Protein kinase domain Domain
Sequence
Sequence length 343
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Creatine deficiency Creatine deficiency, X-linked ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 18562482, 24552815, 33099476
Carcinogenesis Associate 33099476
Carcinoma Hepatocellular Associate 33099476, 35865652
Carcinoma Renal Cell Associate 21253009, 23634203
Carcinoma Renal Cell Stimulate 33099476
Chromosomal Instability Associate 31515286
Chromosome Disorders Associate 31515286
Hypertension Associate 37451613
Mosaic variegated aneuploidy syndrome Associate 31515286
Neoplasm Metastasis Stimulate 33099476