Protein information
  Protein summary    Phosphorylation site    Dephosphorylation site    Mutation site
  Differential expressed protein    Hyperphosphorylation site    Direct interaction pair    Function Annotation

Protein Summary
UniProt/SwissProt ID:RP9_HUMAN
Description:retinitis pigmentosa 9 (autosomal dominant) [Source:HGNC Symbol;Acc:10288]
Location:chr7 p14.3
Node attribute:substrate

Phosphorylation site
PositionPhosphoPeptideCatalytic kinaseSource
Y142HEDPMyDIIRDMed19; Ydc2-catalyt; SR-2PhosphoSitePlus
S214HKSSKsNEGSDPIM1RegPhos
S212RKHKSsKSNEGPIM1RegPhos
Y52HLESFyEKPPPPhosphoSitePlus

Dephosphorylation site
RP9_HUMAN do not have dephosphorylation site.

Mutation site
RP9_HUMAN do not have mutation site.

Differential expressed protein
RP9_HUMAN is not differential expressed protein.

Hyperphosphorylation site
RP9_HUMAN do not have hyperphosphorylation site.

Direct Interaction Pair
SourceTargetRelationshipResource
PIM1_HUMANRP9_HUMANkinase -> substrateRegPhos

Function Annotation
KEGG Pathway
RP9_HUMAN is not in KEGG pathway.

Gene Ontology
GO IDGO_TermEvidenceOntology
GO:0003676nucleic acid bindingIEAmolecular_function
GO:0008380RNA splicingTASbiological_process
GO:0005515protein bindingIEAmolecular_function
GO:0008270zinc ion bindingIEAmolecular_function
GO:0005515protein bindingIPImolecular_function
GO:0005634nucleusIEAcellular_component
GO:0005785signal recognition particle receptor complexIEAcellular_component


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