Gene Gene information from NCBI Gene database.
Entrez ID 5523
Gene name Protein phosphatase 2 regulatory subunit B''alpha
Gene symbol PPP2R3A
Synonyms (NCBI Gene)
PPP2R3PR130PR72
Chromosome 3
Chromosome location 3q22.2-q22.3
Summary 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.
294
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0000159 Component Protein phosphatase type 2A complex IBA
GO:0000159 Component Protein phosphatase type 2A complex IDA 15687260, 17055435
GO:0000159 Component Protein phosphatase type 2A complex ISS 1849734
GO:0001754 Process Eye photoreceptor cell differentiation IGI 15687260
GO:0001756 Process Somitogenesis IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604944 9307 ENSG00000073711
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
52
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs145391296, rs147006675 RCV005936814
RCV005905018
Chronic lymphocytic leukemia/small lymphocytic lymphoma Benign rs200024034 RCV005871452
Clear cell carcinoma of kidney Benign rs147006675 RCV005905019
Familial cancer of breast Benign rs147006675 RCV005905017
Associations from Text MiningDisease associations identified through Pubtator
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