Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5536
Gene name Gene Name - the full gene name approved by the HGNC.
Protein phosphatase 5 catalytic subunit
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PPP5C
Synonyms (NCBI Gene) Gene synonyms aliases
PP5, PPP5, PPT
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.32
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a serine/threonine phosphatase which is a member of the protein phosphatase catalytic subunit family. Proteins in this family participate in pathways regulated by reversible phosphorylation at serine and threonine residues; many of these
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT001518 hsa-miR-155-5p pSILAC 18668040
MIRT039894 hsa-miR-615-3p CLASH 23622248
MIRT039894 hsa-miR-615-3p CLASH 23622248
MIRT038528 hsa-miR-99b-3p CLASH 23622248
MIRT1258599 hsa-miR-4286 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000165 Process MAPK cascade TAS
GO:0000278 Process Mitotic cell cycle TAS 7925273
GO:0001965 Function G-protein alpha-subunit binding IEA
GO:0003723 Function RNA binding IEA
GO:0004721 Function Phosphoprotein phosphatase activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600658 9322 ENSG00000011485
Protein
UniProt ID P53041
Protein name Serine/threonine-protein phosphatase 5 (PP5) (EC 3.1.3.16) (Protein phosphatase T) (PP-T) (PPT)
Protein function Serine/threonine-protein phosphatase that dephosphorylates a myriad of proteins involved in different signaling pathways including the kinases CSNK1E, ASK1/MAP3K5, PRKDC and RAF1, the nuclear receptors NR3C1, PPARG, ESR1 and ESR2, SMAD proteins
PDB 1A17 , 1S95 , 1WAO , 2BUG , 3H60 , 3H61 , 3H62 , 3H63 , 3H64 , 3H66 , 3H67 , 3H68 , 3H69 , 4ZVZ , 4ZX2 , 5HPE , 5UI1 , 5WG8 , 7ZR5 , 7ZR6 , 8GAE , 8GFT
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00515 TPR_1 28 61 Tetratricopeptide repeat Repeat
PF08321 PPP5 136 228 PPP5 TPR repeat region Family
PF00149 Metallophos 235 431 Calcineurin-like phosphoesterase Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:15546861}.
Sequence
Sequence length 499
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  MAPK signaling pathway   Negative regulation of MAPK pathway
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
ESR-mediated signaling
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Crohn Disease Crohn's disease N/A N/A GWAS
Inflammatory Bowel Disease Inflammatory bowel disease N/A N/A GWAS
Neuroticism Neuroticism N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Asthma Associate 27501780
Breast Neoplasms Associate 11331294
Carcinoma Hepatocellular Associate 28453226
Carcinoma Renal Cell Associate 29141220
Colitis Ulcerative Associate 38302916
Colorectal Neoplasms Associate 15004035
Glioma Associate 25796168
Glucocorticoid Receptor Deficiency Associate 27742828
Kidney Neoplasms Associate 29141220
Lymphoma Mantle Cell Associate 15650054