Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5257
Gene name Gene Name - the full gene name approved by the HGNC.
Phosphorylase kinase regulatory subunit beta
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PHKB
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16q12.1
Summary Summary of gene provided in NCBI Entrez Gene.
Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic i
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs34667348 C>A,T Uncertain-significance, pathogenic-likely-pathogenic, conflicting-interpretations-of-pathogenicity Stop gained, missense variant, coding sequence variant
rs61494991 T>C Conflicting-interpretations-of-pathogenicity Synonymous variant, coding sequence variant
rs111734407 T>A,C Pathogenic Coding sequence variant, missense variant
rs121918021 T>A,G Pathogenic Coding sequence variant, stop gained
rs139738333 A>G Conflicting-interpretations-of-pathogenicity, uncertain-significance Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT000890 hsa-miR-15a-5p Microarray 18362358
MIRT000889 hsa-miR-16-5p Microarray 18362358
MIRT041947 hsa-miR-484 CLASH 23622248
MIRT496619 hsa-miR-1265 PAR-CLIP 22291592
MIRT496618 hsa-miR-4258 PAR-CLIP 22291592
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21418524, 25051373, 25416956, 32296183
GO:0005516 Function Calmodulin binding IEA
GO:0005829 Component Cytosol TAS
GO:0005886 Component Plasma membrane IEA
GO:0005964 Component Phosphorylase kinase complex IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
172490 8927 ENSG00000102893
Protein
UniProt ID Q93100
Protein name Phosphorylase b kinase regulatory subunit beta (Phosphorylase kinase subunit beta)
Protein function Phosphorylase b kinase catalyzes the phosphorylation of serine in certain substrates, including troponin I. The beta chain acts as a regulatory unit and modulates the activity of the holoenzyme in response to phosphorylation.
PDB 8JFK , 8JFL , 8XYA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00723 Glyco_hydro_15 47 878 Glycosyl hydrolases family 15 Domain
Sequence
MAGAAGLTAEVSWKVLERRARTKRSGSVYEPLKSINLPRPDNETLWDKLDHYYRIVKSTL
LLYQSPTTGLFPTKTCGGDQKAKIQDSLYCAAGAWALALAYRRIDDDKGRTHELEHSAIK
CMRGILYCYMRQADKVQQFKQDPRPTTCLHSVFNVHTGDELLSYEEYGHLQINAVSLYLL
YLVEMISSGLQIIYNTDEVSFIQNLVFCVERVYRVPDFGVWERGSKYNNGSTELHSSSVG
LAKAALEAINGFNLFGNQGCSWSVIFVDLDAHNRNRQTLCSLLPRESRSHNTDAALLPCI
SYPAFALDDEVLFSQTLDKVVRKLKGKYGFKRFLRDGYRTSLEDPNRCYYKPAEIKLFDG
IECEFPIFFLYMMIDGVFRGNPKQVQEYQDLLTPVLHHTTEGYPVVPKYYYVPADFVEYE
KNNPGSQKRFPSNCGRDGKLFLWGQALYIIAKLLADELISPKDIDPVQRYVPLKDQRNVS
MRFSNQGPLENDLVVHVALIAESQRLQVFLNTYGIQTQTPQQVEPIQIWPQQELVKAYLQ
LGINEKLGLSGRPDRPIGCLGTSKIYRILGKTVVCYPIIFDLSDFYMSQDVFLLIDDIKN
ALQFIKQYWKMHGRPLFLVLIREDNIRGSRFNPILDMLAALKKGIIGGVKVHVDRLQTLI
SGAVVEQLDFLRISDTEELPEFKSFEELEPPKHSKVKRQSSTPSAPELGQQPDVNISEWK
DKPTHEILQKLNDCSCLASQAILLGILLKREGPNFITKEGTVSDHIERVYRRAGSQKLWL
AVRYGAAFTQKFSSSIAPHITTFLVHGKQVTLGAFGHEEEVISNPLSPRVIQNIIYYKCN
THDEREAVIQQELVIHIGWIISNNPELFSGMLKIRIGW
IIHAMEYELQIRGGDKPALDLY
QLSPSEVKQLLLDILQPQQNGRCWLNRRQIDGSLNRTPTGFYDRVWQILERTPNGIIVAG
KHLPQQPTLSDMTMYEMNFSLLVEDTLGNIDQPQYRQIVVELLMVVSIVLERNPELEFQD
KVDLDRLVKEAFNEFQKDQSRLKEIEKQDDMTSFYNTPPLGKRGTCSYLTKAVMNLLLEG
EVKPNNDDPCLIS
Sequence length 1093
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
Insulin signaling pathway
Glucagon signaling pathway
  Glycogen breakdown (glycogenolysis)
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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
Glycogen Storage Disease glycogen storage disease ixb, Glycogen phosphorylase kinase deficiency rs1242540921, rs797044442, rs371296953, rs121918021, rs1303617854, rs1322527832, rs199948078, rs758004953, rs145166656, rs149244943, rs34667348, rs748262135 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
Strabismus Strabismus N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Inhibit 31754332
Carcinoma Squamous Cell Associate 24929328
Glycogen Storage Disease Type II Associate 38212860
Glycogen Storage Disease Type Ix Associate 9326319
Glycogen Storage Disease Type VI Associate 9326319
Hepatomegaly Associate 38212860
Hereditary pancreatitis Associate 37603299
Hirschsprung Disease Associate 29093530
Lung Neoplasms Associate 24929328
Neoplasms Associate 25051373, 31754332