MGP Database

MGP002510

Ontology/Pathway Information

Entrez Gene ID5727
Gene Namepatched 1
Gene Symbol PTCH1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0044295 IEA:EnsemblCaxonal growth cone
GO:0005901 IDA:BHF-UCLCcaveola
GO:0044294 IEA:EnsemblCdendritic growth cone
GO:0016021 IEA:UniProtKB-KWCintegral component of membrane
GO:0043231 IDA:BHF-UCLCintracellular membrane-bounded organelle
GO:0030496 IEA:EnsemblCmidbody
GO:0048471 IDA:BHF-UCLCperinuclear region of cytoplasm
GO:0005886 IDA:BHF-UCLCplasma membrane
GO:0014069 IEA:EnsemblCpostsynaptic density
GO:0072372 IEA:EnsemblCprimary cilium
GO:0015485 IDA:BHF-UCLFcholesterol binding
GO:0030332 IPI:BHF-UCLFcyclin binding
GO:0097108 IPI:BHF-UCLFhedgehog family protein binding
GO:0008158 IEA:InterProFhedgehog receptor activity
GO:0008201 IEA:EnsemblFheparin binding
GO:0005119 IPI:BHF-UCLFsmoothened binding
GO:0007420 ISS:BHF-UCLPbrain development
GO:0001658 IEA:EnsemblPbranching involved in ureteric bud morphogenesis
GO:0061005 IEA:EnsemblPcell differentiation involved in kidney development
GO:0072203 IEA:EnsemblPcell proliferation involved in metanephros development
GO:0071397 IMP:BHF-UCLPcellular response to cholesterol
GO:0009953 ISS:UniProtKBPdorsal/ventral pattern formation
GO:0030326 ISS:UniProtKBPembryonic limb morphogenesis
GO:0048568 IEA:EnsemblPembryonic organ development
GO:0008544 IEA:EnsemblPepidermis development
GO:0042593 IEA:EnsemblPglucose homeostasis
GO:0003007 IEA:EnsemblPheart morphogenesis
GO:0035137 IEA:EnsemblPhindlimb morphogenesis
GO:0001701 IEA:EnsemblPin utero embryonic development
GO:0043616 IEA:EnsemblPkeratinocyte proliferation
GO:0035108 IMP:BHF-UCLPlimb morphogenesis
GO:0060603 IEA:EnsemblPmammary gland duct morphogenesis
GO:0060644 IEA:EnsemblPmammary gland epithelial cell differentiation
GO:0051782 IEA:EnsemblPnegative regulation of cell division
GO:0050680 IEA:EnsemblPnegative regulation of epithelial cell proliferation
GO:0040015 ISS:UniProtKBPnegative regulation of multicellular organism growth
GO:0045668 IMP:BHF-UCLPnegative regulation of osteoblast differentiation
GO:0043433 IMP:BHF-UCLPnegative regulation of sequence-specific DNA binding transcription factor activity
GO:0045879 ISS:BHF-UCLPnegative regulation of smoothened signaling pathway
GO:0000122 IMP:BHF-UCLPnegative regulation of transcription from RNA polymerase II promoter
GO:0021997 ISS:BHF-UCLPneural plate axis specification
GO:0001843 IEA:EnsemblPneural tube closure
GO:0021532 IMP:BHF-UCLPneural tube patterning
GO:0009887 ISS:UniProtKBPorgan morphogenesis
GO:0060037 IMP:BHF-UCLPpharyngeal system development
GO:0010875 IDA:BHF-UCLPpositive regulation of cholesterol efflux
GO:0016485 ISS:UniProtKBPprotein processing
GO:0072661 IDA:BHF-UCLPprotein targeting to plasma membrane
GO:0007346 IEA:EnsemblPregulation of mitotic cell cycle
GO:0032880 IEA:EnsemblPregulation of protein localization
GO:0008589 ISS:UniProtKBPregulation of smoothened signaling pathway
GO:0072001 IEP:UniProtKBPrenal system development
GO:0010157 IEA:EnsemblPresponse to chlorate
GO:0042493 IEA:EnsemblPresponse to drug
GO:0032355 IEA:EnsemblPresponse to estradiol
GO:0009612 IEA:EnsemblPresponse to mechanical stimulus
GO:0032526 IEA:EnsemblPresponse to retinoic acid
GO:0007224 IEP:UniProtKBPsmoothened signaling pathway
GO:0060831 IEA:EnsemblPsmoothened signaling pathway involved in dorsal/ventral neural tube patterning
GO:0061053 IMP:BHF-UCLPsomite development
GO:0021522 IEA:EnsemblPspinal cord motor neuron differentiation
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_18372Class B/2 (Secretin family receptors)
REACT_267874Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD)
REACT_116125Disease
REACT_21340GPCR ligand binding
REACT_268323Hedgehog 'off' state
REACT_268718Hedgehog 'on' state
REACT_268573Ligand-receptor interactions
REACT_267615Metabolic disorders of biological oxidation enzymes
REACT_14797Signaling by GPCR
REACT_264508Signaling by Hedgehog
REACT_111102Signal Transduction
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