Gene Gene information from NCBI Gene database.
Entrez ID 10369
Gene name Calcium voltage-gated channel auxiliary subunit gamma 2
Gene symbol CACNG2
Synonyms (NCBI Gene)
MRD10
Chromosome 22
Chromosome location 22q12.3
Summary The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. The AMPA subtype of ionotropic glutamate receptors are ligand gated ion channels
miRNA miRNA information provided by mirtarbase database.
132
miRTarBase ID miRNA Experiments Reference
MIRT659915 hsa-miR-8080 HITS-CLIP 23824327
MIRT659914 hsa-miR-6729-3p HITS-CLIP 23824327
MIRT659913 hsa-miR-6758-3p HITS-CLIP 23824327
MIRT659912 hsa-miR-26b-3p HITS-CLIP 23824327
MIRT659911 hsa-miR-2117 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
50
GO ID Ontology Definition Evidence Reference
GO:0005245 Function Voltage-gated calcium channel activity IBA
GO:0005245 Function Voltage-gated calcium channel activity IEA
GO:0005245 Function Voltage-gated calcium channel activity TAS 10221464
GO:0005262 Function Calcium channel activity IEA
GO:0005515 Function Protein binding IPI 20805473, 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602911 1406 ENSG00000166862
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y698
Protein name Voltage-dependent calcium channel gamma-2 subunit (Neuronal voltage-gated calcium channel gamma-2 subunit) (Transmembrane AMPAR regulatory protein gamma-2) (TARP gamma-2)
Protein function Regulates the trafficking and gating properties of AMPA-selective glutamate receptors (AMPARs). Promotes their targeting to the cell membrane and synapses and modulates their gating properties by slowing their rates of activation, deactivation a
PDB 6DLZ , 6DM0 , 6DM1 , 6O9G , 6TNO
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00822 PMP22_Claudin 6 197 PMP-22/EMP/MP20/Claudin family Family
Tissue specificity TISSUE SPECIFICITY: Brain.
Sequence
MGLFDRGVQMLLTTVGAFAAFSLMTIAVGTDYWLYSRGVCKTKSVSENETSKKNEEVMTH
SGLWRTCCLEGNFKGLCKQIDHFPEDADYEADTAEYFLRAVRASSIFPILSVILLFMGGL
CIAASEFYKTRHNIILSAGIFFVSAGLSNIIGIIVYISANAGDPSKSDSKKNSYSYGWSF
YFGALSFIIAEMVGVLA
VHMFIDRHKQLRATARATDYLQASAITRIPSYRYRYQRRSRSS
SRSTEPSHSRDASPVGIKGFNTLPSTEISMYTLSRDPLKAATTPTATYNSDRDNSFLQVH
NCIQKENKDSLHSNTANRRTTPV
Sequence length 323
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  MAPK signaling pathway
Cardiac muscle contraction
Adrenergic signaling in cardiomyocytes
Oxytocin signaling pathway
Hypertrophic cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy
Dilated cardiomyopathy
  Presynaptic depolarization and calcium channel opening
Trafficking of AMPA receptors
Phase 0 - rapid depolarisation
Phase 2 - plateau phase
LGI-ADAM interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
16
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
CACNG2-related disorder Uncertain significance; Benign; Likely benign rs139052540, rs571563795, rs149442040 RCV003955395
RCV003921748
RCV003902953
Complex neurodevelopmental disorder Uncertain significance rs915061917 RCV005356439
Ependymoma Uncertain significance rs1555892196 RCV000577842
Gastric cancer Likely benign rs146357556 RCV005900766
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Bipolar Disorder Associate 23038240, 25730879, 30738251
Breast Cancer Lymphedema Associate 30371558
Chronic Pain Associate 30371558
Epilepsy Associate 18565486
Epilepsy Absence Associate 20561025
Glioblastoma Associate 35788194
Hippocampal Sclerosis Associate 32189710
Hyperalgesia Associate 35776036
Mandibular Nerve Injuries Associate 30371558
Nerve Degeneration Associate 35776036