Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5528
Gene name Gene Name - the full gene name approved by the HGNC.
Protein phosphatase 2 regulatory subunit B'delta
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PPP2R5D
Synonyms (NCBI Gene) Gene synonyms aliases
B56D, B56delta, HJS1, MRD35
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.1
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
MIRT040037 hsa-miR-615-3p CLASH 23622248
MIRT040037 hsa-miR-615-3p CLASH 23622248
MIRT040037 hsa-miR-615-3p CLASH 23622248
MIRT035781 hsa-miR-1914-5p CLASH 23622248
MIRT535065 hsa-miR-371b-3p PAR-CLIP 20371350
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
GO:0000159 Component Protein phosphatase type 2A complex IEA
GO:0005515 Function Protein binding IPI 16189514, 16541025, 17540176, 18782753, 19293187, 21666598, 22976297, 23555304, 24157919, 25416956, 26496610, 27173435, 28330616, 29892012, 30595372, 32296183, 33961781
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601646 9312 ENSG00000112640
Protein
UniProt ID Q14738
Protein name Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta isoform (PP2A B subunit isoform B'-delta) (PP2A B subunit isoform B56-delta) (PP2A B subunit isoform PR61-delta) (PP2A B subunit isoform R5-delta)
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 8U1X , 8U89
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01603 B56 103 513 Protein phosphatase 2A regulatory B subunit (B56 family) Family
Tissue specificity TISSUE SPECIFICITY: Isoform Delta-2 is widely expressed. Isoform Delta-1 is highly expressed in brain.
Sequence
Sequence length 602
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
seizure Seizure rs1064794719 N/A
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
Mental retardation syndromic intellectual disability N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alcohol Related Disorders Associate 33482199
Autism Spectrum Disorder Associate 26576547, 33482199, 37167322, 37572851
Autistic Disorder Associate 26576547, 37339871
Colorectal Neoplasms Associate 28105922
Congenital Abnormalities Associate 26576547
Developmental Disabilities Associate 32743835, 33628804, 34946857, 37339871
Fibrous Dysplasia Polyostotic Associate 37339871, 37572851
Fragile X Syndrome Associate 34946857
Genetic Diseases Inborn Associate 33628804
Hepatitis C Associate 35836293