Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10368
Gene name Gene Name - the full gene name approved by the HGNC.
Calcium voltage-gated channel auxiliary subunit gamma 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CACNG3
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16p12.1
Summary Summary of gene provided in NCBI Entrez Gene.
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. This gene is part of a functionally diverse eight-member protein subfamily of the
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029027 hsa-miR-26b-5p Microarray 19088304
MIRT858069 hsa-miR-299-3p CLIP-seq
MIRT858070 hsa-miR-3117-3p CLIP-seq
MIRT858071 hsa-miR-3169 CLIP-seq
MIRT858072 hsa-miR-3184 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005245 Function Voltage-gated calcium channel activity IBA 21873635
GO:0005245 Function Voltage-gated calcium channel activity NAS 10221464
GO:0005886 Component Plasma membrane TAS
GO:0005891 Component Voltage-gated calcium channel complex NAS 10221464
GO:0006605 Process Protein targeting ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606403 1407 ENSG00000006116
Protein
UniProt ID O60359
Protein name Voltage-dependent calcium channel gamma-3 subunit (Neuronal voltage-gated calcium channel gamma-3 subunit) (Transmembrane AMPAR regulatory protein gamma-3) (TARP gamma-3)
Protein function Regulates the trafficking to the somatodendritic compartment 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
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00822 PMP22_Claudin 6 196 PMP-22/EMP/MP20/Claudin family Family
Sequence
Sequence length 315
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Metabolic Syndrome Metabolic Syndrome GWAS
Oligodendroglioma Oligodendroglioma GWAS
Prostate cancer Prostate cancer Together, these results show that PRRX2 is an oncogene and might play a role in the aggressiveness of PC within the DNPC population. GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Pancreatic Ductal Associate 37794108
Epilepsy Absence Associate 17264864
Glioma Inhibit 37697240
Leukemia Promyelocytic Acute Associate 21169531
Macular Degeneration Associate 21169531
Neoplasms Associate 26209800