Gene Gene information from NCBI Gene database.
Entrez ID 817
Gene name Calcium/calmodulin dependent protein kinase II delta
Gene symbol CAMK2D
Synonyms (NCBI Gene)
CAMKD
Chromosome 4
Chromosome location 4q26
Summary The product of this gene belongs to the serine/threonine protein kinase family and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. In mammalian cells, t
miRNA miRNA information provided by mirtarbase database.
574
miRTarBase ID miRNA Experiments Reference
MIRT025927 hsa-miR-7-5p Microarray 19073608
MIRT052455 hsa-let-7a-5p CLASH 23622248
MIRT041998 hsa-miR-484 CLASH 23622248
MIRT860194 hsa-miR-1224-5p CLIP-seq
MIRT860195 hsa-miR-1229 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
68
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0001558 Process Regulation of cell growth NAS 9060999
GO:0002026 Process Regulation of the force of heart contraction TAS 23283722
GO:0003254 Process Regulation of membrane depolarization IDA 22514276
GO:0004672 Function Protein kinase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607708 1462 ENSG00000145349
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q13557
Protein name Calcium/calmodulin-dependent protein kinase type II subunit delta (CaM kinase II subunit delta) (CaMK-II subunit delta) (EC 2.7.11.17)
Protein function Calcium/calmodulin-dependent protein kinase involved in the regulation of Ca(2+) homeostatis and excitation-contraction coupling (ECC) in heart by targeting ion channels, transporters and accessory proteins involved in Ca(2+) influx into the myo
PDB 2VN9 , 2W2C , 2WEL , 3GP2 , 5VLO , 6AYW , 7ZRP , 7ZRQ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 14 272 Protein kinase domain Domain
PF08332 CaMKII_AD 346 473 Calcium/calmodulin dependent protein kinase II association domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in cardiac muscle and skeletal muscle. Isoform Delta 3, isoform Delta 2, isoform Delta 8 and isoform Delta 9 are expressed in cardiac muscle. Isoform Delta 11 is expressed in skeletal muscle. {ECO:0000269|PubMed:10189359, ECO
Sequence
Sequence length 499
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  ErbB signaling pathway
Calcium signaling pathway
cAMP signaling pathway
HIF-1 signaling pathway
Oocyte meiosis
Efferocytosis
Necroptosis
Adrenergic signaling in cardiomyocytes
Wnt signaling pathway
Axon guidance
Circadian entrainment
Long-term potentiation
Neurotrophin signaling pathway
Cholinergic synapse
Dopaminergic synapse
Olfactory transduction
Inflammatory mediator regulation of TRP channels
Insulin secretion
GnRH signaling pathway
Melanogenesis
Oxytocin signaling pathway
Glucagon signaling pathway
Aldosterone synthesis and secretion
Cushing syndrome
Gastric acid secretion
Parkinson disease
Pathways of neurodegeneration - multiple diseases
Amphetamine addiction
Tuberculosis
Pathways in cancer
Proteoglycans in cancer
Glioma
Diabetic cardiomyopathy
Lipid and atherosclerosis
  HSF1-dependent transactivation
Trafficking of AMPA receptors
Unblocking of NMDA receptors, glutamate binding and activation
Phase 0 - rapid depolarisation
Ion homeostasis
RAF activation
RAF/MAP kinase cascade
Signaling by moderate kinase activity BRAF mutants
Signaling by BRAF and RAF fusions
Paradoxical activation of RAF signaling by kinase inactive BRAF
Interferon gamma signaling
Ion transport by P-type ATPases
Signaling downstream of RAS mutants
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
9
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
CAMK2D-related condition Likely pathogenic rs2511649109 RCV005242107
Neurodevelopmental disorder Pathogenic; Likely pathogenic rs2098989283, rs2515933527, rs2512545072, rs2511651497, rs2511651126, rs2511649293, rs2511649109 RCV002282583
RCV002282584
RCV002282585
RCV002282586
RCV002282587
RCV002282588
RCV002282589
See cases Pathogenic rs867010473 RCV003319549
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Bipolar Disorder Associate 27063557
Breast Neoplasms Inhibit 33742056
Carcinoma Ovarian Epithelial Associate 21447778
Cardiomyopathy Dilated Associate 37372357
Cerebral Small Vessel Diseases Associate 32047268
Colitis Ulcerative Associate 38274809
Colorectal Neoplasms Associate 22095101
Congenital Hyperinsulinism Associate 23869231
Developmental Disabilities Associate 37372357
Drug Resistant Epilepsy Associate 40646440