Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5526
Gene name Gene Name - the full gene name approved by the HGNC.
Protein phosphatase 2 regulatory subunit B'beta
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PPP2R5B
Synonyms (NCBI Gene) Gene synonyms aliases
B56B, B56beta, PR61B
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.1
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000159 Component Protein phosphatase type 2A complex IBA 21873635
GO:0005515 Function Protein binding IPI 7592815, 15380617, 16456541, 18782753, 28330616, 30595372, 32296183
GO:0005634 Component Nucleus IBA 21873635
GO:0005737 Component Cytoplasm TAS 8703017
GO:0005829 Component Cytosol IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601644 9310 ENSG00000068971
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Oligodendroglioma Oligodendroglioma GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 33712023, 36028814, 37923899
Simpson Golabi Behmel syndrome Associate 25972378