Gene Gene information from NCBI Gene database.
Entrez ID 5533
Gene name Protein phosphatase 3 catalytic subunit gamma
Gene symbol PPP3CC
Synonyms (NCBI Gene)
CALNA3CNA3PP2Bgamma
Chromosome 8
Chromosome location 8p21.3
Summary Calcineurin is a calcium-dependent, calmodulin-stimulated protein phosphatase involved in the downstream regulation of dopaminergic signal transduction. Calcineurin is composed of a regulatory subunit and a catalytic subunit. The protein encoded by this g
miRNA miRNA information provided by mirtarbase database.
31
miRTarBase ID miRNA Experiments Reference
MIRT714710 hsa-miR-3922-5p HITS-CLIP 19536157
MIRT714709 hsa-miR-6832-3p HITS-CLIP 19536157
MIRT714708 hsa-miR-655-5p HITS-CLIP 19536157
MIRT714707 hsa-miR-377-5p HITS-CLIP 19536157
MIRT714705 hsa-miR-6086 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
GO ID Ontology Definition Evidence Reference
GO:0004721 Function Phosphoprotein phosphatase activity IEA
GO:0004722 Function Protein serine/threonine phosphatase activity IEA
GO:0004723 Function Calcium-dependent protein serine/threonine phosphatase activity IDA 26429887
GO:0005515 Function Protein binding IPI 25416956, 28514442, 32296183, 32814053, 33961781, 34446558
GO:0005516 Function Calmodulin binding IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
114107 9316 ENSG00000120910
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P48454
Protein name Serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform (EC 3.1.3.16) (CAM-PRP catalytic subunit) (Calcineurin, testis-specific catalytic subunit) (Calmodulin-dependent calcineurin A subunit gamma isoform)
Protein function Calcium-dependent, calmodulin-stimulated protein phosphatase which plays an essential role in the transduction of intracellular Ca(2+)-mediated signals. Dephosphorylates and activates transcription factor NFATC1. Dephosphorylates and inactivates
PDB 7U0T
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00149 Metallophos 79 281 Calcineurin-like phosphoesterase Domain
Tissue specificity TISSUE SPECIFICITY: Testis. {ECO:0000269|PubMed:1339277}.
Sequence
MSGRRFHLSTTDRVIKAVPFPPTQRLTFKEVFENGKPKVDVLKNHLVKEGRLEEEVALKI
INDGAAILRQEKTMIEVDAPITVCGDIHGQFFDLMKLFEVGGSPSNTRYLFLGDYVDRGY
FSIECVLYLWSLKINHPKTLFLLRGNHECRHLTDYFTFKQECRIKYSEQVYDACMETFDC
LPLAALLNQQFLCVHGGMSPEITSLDDIRKLDRFTEPPAFGPVCDLLWSDPSEDYGNEKT
LEHYTHNTVRGCSYFYSYPAVCEFLQNNNLLSIIRAHEAQD
AGYRMYRKSQATGFPSLIT
IFSAPNYLDVYNNKAAVLKYENNVMNIRQFNCSPHPYWLPNFMDVFTWSLPFVGEKVTEM
LVNVLNICSDDELISDDEAEGSTTVRKEIIRNKIRAIGKMARVFSILRQESESVLTLKGL
TPTGTLPLGVLSGGKQTIETATVEAVEAREAIRGFSLQHKIRSFEEARGLDRINERMPPR
KDSIHAGGPMKSVTSAHSHAAHRSDQGKKAHS
Sequence length 512
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  MAPK signaling pathway
Calcium signaling pathway
cGMP-PKG signaling pathway
Oocyte meiosis
Cellular senescence
Wnt signaling pathway
Axon guidance
VEGF signaling pathway
Osteoclast differentiation
C-type lectin receptor signaling pathway
Natural killer cell mediated cytotoxicity
Th1 and Th2 cell differentiation
Th17 cell differentiation
T cell receptor signaling pathway
B cell receptor signaling pathway
Long-term potentiation
Glutamatergic synapse
Dopaminergic synapse
Oxytocin signaling pathway
Glucagon signaling pathway
Renin secretion
Alzheimer disease
Amyotrophic lateral sclerosis
Prion disease
Pathways of neurodegeneration - multiple diseases
Amphetamine addiction
Tuberculosis
Human cytomegalovirus infection
Human T-cell leukemia virus 1 infection
Kaposi sarcoma-associated herpesvirus infection
Human immunodeficiency virus 1 infection
PD-L1 expression and PD-1 checkpoint pathway in cancer
Lipid and atherosclerosis
  Activation of BAD and translocation to mitochondria
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Keratoconus Uncertain significance rs1563790727 RCV000678667
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Brain Injuries Associate 27225880
Carcinoma Non Small Cell Lung Inhibit 38167059
Carcinoma Ovarian Epithelial Associate 34573382
Hypertension Stimulate 29237677
Mental Disorders Associate 25571521, 27225880, 34318684
Neoplasms Associate 18460741, 38167059
Neoplasms Inhibit 34573382
Obesity Associate 37399741
Pancreatic Neoplasms Associate 33270085
Prostatic Neoplasms Inhibit 18460741