Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5523
Gene name Gene Name - the full gene name approved by the HGNC.
Protein phosphatase 2 regulatory subunit B''alpha
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PPP2R3A
Synonyms (NCBI Gene) Gene synonyms aliases
PPP2R3, PR130, PR72
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q22.2-q22.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes one of the regulatory subunits of the protein phosphatase 2. Protein phosphatase 2 (formerly named type 2A) is one of the four major Ser/Thr phosphatases and is implicated in the negative control of cell growth and division. Protein phos
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019482 hsa-miR-148b-3p Microarray 17612493
MIRT649473 hsa-miR-4759 HITS-CLIP 23824327
MIRT649472 hsa-miR-3169 HITS-CLIP 23824327
MIRT649471 hsa-miR-8083 HITS-CLIP 23824327
MIRT621045 hsa-miR-6814-5p HITS-CLIP 23824327
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:0000159 Component Protein phosphatase type 2A complex IDA 17055435
GO:0000159 Component Protein phosphatase type 2A complex ISS 1849734
GO:0005509 Function Calcium ion binding IEA
GO:0005515 Function Protein binding IPI 9847399, 30595372
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604944 9307 ENSG00000073711
Protein
UniProt ID Q06190
Protein name Serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit alpha (PP2A subunit B isoform PR72/PR130) (PP2A subunit B isoform R3 isoform) (PP2A subunit B isoforms B''-PR72/PR130) (PP2A subunit B isoforms B72/B130) (Serine/threonine-protein phos
Protein function The B regulatory subunit might modulate substrate selectivity and catalytic activity, and might also direct the localization of the catalytic enzyme to a particular subcellular compartment.
PDB 4I5J , 4I5K
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17958 EF-hand_13 796 885 EF-hand domain Domain
PF13499 EF-hand_7 900 1002 EF-hand domain pair Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in heart, brain, placenta, lung, muscle and kidney.
Sequence
MAATYRLVVSTVNHYSSVVIDRRFEQAIHYCTGTCHTFTHGIDCIVVHHSVCADLLHIPV
SQFKDADLNSMFLPHENGLSSAEGDYPQQAFTGIPRVKRGSTFQNTYNLKDIAGEAISFA
SGKIKEFSFEKLKNSNHAAYRKGRKVKSDSFNRRSVDLDLLCGHYNNDGNAPSFGLLRSS
SVEEKPLSHRNSLDTNLTSMFLQNFSEEDLVTQILEKHKIDNFSSGTDIKMCLDILLKCS
EDLKKCTDIIKQCIKKKSGSSISEGSGNDTISSSETVYMNVMTRLASYLKKLPFEFMQSG
NNEALDLTELISNMPSLQLTPFSPVFGTEQPPKYEDVVQLSASDSGRFQTIELQNDKPNS
RKMDTVQSIPNNSTNSLYNLEVNDPRTLKAVQVQSQSLTMNPLENVSSDDLMETLYIEEE
SDGKKALDKGQKTENGPSHELLKVNEHRAEFPEHATHLKKCPTPMQNEIGKIFEKSFVNL
PKEDCKSKVSKFEEGDQRDFTNSSSQEEIDKLLMDLESFSQKMETSLREPLAKGKNSNFL
NSHSQLTGQTLVDLEPKSKVSSPIEKVSPSCLTRIIETNGHKIEEEDRALLLRILESIED
FAQELVECKSSRGSLSQEKEMMQILQETLTTSSQANLSVCRSPVGDKAKDTTSAVLIQQT
PEVIKIQNKPEKKPGTPLPPPATSPSSPRPLSPVPHVNNVVNAPLSINIPRFYFPEGLPD
TCSNHEQTLSRIETAFMDIEEQKADIYEMGKIAKVCGCPLYWKAPMFRAAGGEKTGFVTA
QSFIAMWRKLLNNHHDDASKFICLLAKPNCSSLEQEDFIPLLQDVVDTHPGLTFLKDAPE
FHSRYITTVIQRIFYTVNRSWSGKITSTEIRKSNFLQTLALLEEE
EDINQITDYFSYEHF
YVIYCKFWELDTDHDLYISQADLSRYNDQASSSRIIERIFSGAVTRGKTIQKEGRMSYAD
FVWFLISEEDKRNPTSIEYWFRCMDVDGDGVLSMYELEYFYE
EQCERMEAMGIEPLPFHD
LLCQMLDLVKPAVDGKITLRDLKRCRMAHIFYDTFFNLEKYLDHEQRDPFAVQKDVENDG
PEPSDWDRFAAEEYETLVAEESAQAQFQEGFEDYETDEPASPSEFGNKSNKILSASLPEK
CGKLQSVDEE
Sequence length 1150
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Schizophrenia Schizophrenia GWAS
Neuroticism Neuroticism GWAS
Myocardial Infarction Myocardial Infarction GWAS
Atrial Fibrillation Atrial Fibrillation GWAS
Associations from Text Mining
Disease Name Relationship Type References
Ataxia Telangiectasia Associate 19430199
Carcinoma Hepatocellular Associate 35945177
Fibrosarcoma Associate 26945059
Hepatitis B Associate 19430199
Leukemia Associate 19430199
Lipoma Associate 26945059
Lymphoma Non Hodgkin Associate 36788429
Neoplasms Associate 19430199, 35945177
Pancreatic Neoplasms Associate 35077391
Precursor Cell Lymphoblastic Leukemia Lymphoma Associate 19430199