Gene Gene information from NCBI Gene database.
Entrez ID 5526
Gene name Protein phosphatase 2 regulatory subunit B'beta
Gene symbol PPP2R5B
Synonyms (NCBI Gene)
B56BB56betaPR61B
Chromosome 11
Chromosome location 11q13.1
Summary The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common het
miRNA miRNA information provided by mirtarbase database.
121
miRTarBase ID miRNA Experiments Reference
MIRT1257980 hsa-miR-1197 CLIP-seq
MIRT1257981 hsa-miR-1237 CLIP-seq
MIRT1257982 hsa-miR-1257 CLIP-seq
MIRT1257983 hsa-miR-216b CLIP-seq
MIRT1257984 hsa-miR-3127-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0000159 Component Protein phosphatase type 2A complex IBA
GO:0000159 Component Protein phosphatase type 2A complex IEA
GO:0005515 Function Protein binding IPI 7592815, 15380617, 16456541, 18782753, 27880917, 28330616, 30595372, 32296183, 33961781, 35271311
GO:0005634 Component Nucleus IBA
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601644 9310 ENSG00000068971
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q15173
Protein name Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit beta isoform (PP2A B subunit isoform B'-beta) (PP2A B subunit isoform B56-beta) (PP2A B subunit isoform PR61-beta) (PP2A B subunit isoform R5-beta)
Protein function As the regulatory component of the serine/threonine-protein phosphatase 2A (PP2A) holoenzyme, modulates substrate specificity, subcellular localization, and responsiveness to phosphorylation. The phosphorylated form mediates the interaction betw
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01603 B56 62 467 Protein phosphatase 2A regulatory B subunit (B56 family) Family
Tissue specificity TISSUE SPECIFICITY: Highest expression in brain.
Sequence
Sequence length 497
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
9
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Adrenocortical carcinoma, hereditary Benign rs111934356 RCV005926010
Colorectal cancer Benign rs111934356 RCV005926011
Lymphoma Benign rs111934356 RCV005926012
Nonpapillary renal cell carcinoma Benign rs111934356 RCV005926009
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 33712023, 36028814, 37923899
Simpson Golabi Behmel syndrome Associate 25972378