MGP Database

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MGP004496

Ontology/Pathway Information

Entrez Gene ID11261
Gene Namecalcineurin-like EF-hand protein 1
Gene Symbol CHP1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005737 ISS:UniProtKBCcytoplasm
GO:0005829 IEA:EnsemblCcytosol
GO:0005783 ISS:UniProtKBCendoplasmic reticulum
GO:0005793 IEA:UniProtKB-SubCellCendoplasmic reticulum-Golgi intermediate compartment
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005925 IDA:UniProtKBCfocal adhesion
GO:0000139 ISS:UniProtKBCGolgi membrane
GO:0015630 ISS:UniProtKBCmicrotubule cytoskeleton
GO:0005634 ISS:UniProtKBCnucleus
GO:0005886 IDA:UniProtKBCplasma membrane
GO:0030133 ISS:UniProtKBCtransport vesicle
GO:0048306 IDA:UniProtKBFcalcium-dependent protein binding
GO:0005509 IDA:UniProtKBFcalcium ion binding
GO:0019900 ISS:UniProtKBFkinase binding
GO:0008017 ISS:UniProtKBFmicrotubule binding
GO:0015459 TAS:ProtIncFpotassium channel regulator activity
GO:0004860 IEA:UniProtKB-KWFprotein kinase inhibitor activity
GO:0005215 ISS:UniProtKBFtransporter activity
GO:0017156 IEA:EnsemblPcalcium ion-dependent exocytosis
GO:0071468 ISS:UniProtKBPcellular response to acidic pH
GO:0031122 ISS:UniProtKBPcytoplasmic microtubule organization
GO:0022406 ISS:UniProtKBPmembrane docking
GO:0061025 ISS:UniProtKBPmembrane fusion
GO:0061024 ISS:UniProtKBPmembrane organization
GO:0001578 ISS:UniProtKBPmicrotubule bundle formation
GO:0070885 IDA:UniProtKBPnegative regulation of calcineurin-NFAT signaling cascade
GO:0032088 IDA:UniProtKBPnegative regulation of NF-kappaB transcription factor activity
GO:0010923 IDA:UniProtKBPnegative regulation of phosphatase activity
GO:0031953 ISS:UniProtKBPnegative regulation of protein autophosphorylation
GO:0042308 IDA:UniProtKBPnegative regulation of protein import into nucleus
GO:0006469 ISS:UniProtKBPnegative regulation of protein kinase activity
GO:0001933 ISS:UniProtKBPnegative regulation of protein phosphorylation
GO:0031397 ISS:UniProtKBPnegative regulation of protein ubiquitination
GO:0060050 ISS:UniProtKBPpositive regulation of protein glycosylation
GO:0090314 ISS:UniProtKBPpositive regulation of protein targeting to membrane
GO:0051222 ISS:UniProtKBPpositive regulation of protein transport
GO:0032417 IDA:UniProtKBPpositive regulation of sodium:proton antiporter activity
GO:0006813 TAS:ProtIncPpotassium ion transport
GO:0006611 ISS:UniProtKBPprotein export from nucleus
GO:0051259 IEA:EnsemblPprotein oligomerization
GO:0050821 ISS:UniProtKBPprotein stabilization
GO:0051453 IDA:UniProtKBPregulation of intracellular pH
GO:1901214 IMP:UniProtKBPregulation of neuron death
GO:0007264 TAS:ProtIncPsmall GTPase mediated signal transduction
GO:0045056 IEA:EnsemblPtranscytosis
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_268678Defective B3GAT3 causes JDSSDHD
REACT_268431Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
REACT_268749Defective B4GALT7 causes EDS, progeroid type
REACT_267917Defective CHST14 causes EDS, musculocontractural type
REACT_267648Defective CHST3 causes SEDCJD
REACT_268786Defective CHST6 causes MCDC1
REACT_268113Defective CHSY1 causes TPBS
REACT_267942Defective EXT1 causes exostoses 1, TRPS2 and CHDS
REACT_267741Defective EXT2 causes exostoses 2
REACT_268843Defective PAPSS2 causes SEMD-PA
REACT_268059Defective SLC26A2 causes chondrodysplasias
REACT_116125Disease
REACT_268624Diseases associated with glycosaminoglycan metabolism
REACT_268324Diseases of glycosylation
REACT_264090Glycogen storage diseases
REACT_121315Glycosaminoglycan metabolism
REACT_121083Hyaluronan metabolism
REACT_120996Hyaluronan uptake and degradation
REACT_111217Metabolism
REACT_474Metabolism of carbohydrates
REACT_147857MPS I - Hurler syndrome
REACT_147734MPS II - Hunter syndrome
REACT_147753MPS IIIA - Sanfilippo syndrome A
REACT_147788MPS IIIB - Sanfilippo syndrome B
REACT_147860MPS IIIC - Sanfilippo syndrome C
REACT_147749MPS IIID - Sanfilippo syndrome D
REACT_147825MPS IV - Morquio syndrome A
REACT_147798MPS IV - Morquio syndrome B
REACT_147739MPS IX - Natowicz syndrome
REACT_147759MPS VII - Sly syndrome
REACT_147719MPS VI - Maroteaux-Lamy syndrome
REACT_147853Mucopolysaccharidoses
REACT_264430Myoclonic epilepsy of Lafora
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