Cancer Cell Metabolism Gene Database

  Cancer Cell Metabolism Gene DB

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Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory
Cross referenced IDs for 5080
* We obtained these cross-references from Uniprot database. It covers 150 different DBs, 18 categories. http://www.uniprot.org/help/cross_references_section
DB CategoryDB NameDB's ID and Url link
Genome annotation databasesEnsembl ENST00000241001; ENSP00000241001; ENSG00000007372. [P26367-1]
Genome annotation databasesEnsembl ENST00000379107; ENSP00000368401; ENSG00000007372. [P26367-2]
Genome annotation databasesEnsembl ENST00000379109; ENSP00000368403; ENSG00000007372. [P26367-1]
Genome annotation databasesEnsembl ENST00000379111; ENSP00000368406; ENSG00000007372. [P26367-1]
Genome annotation databasesEnsembl ENST00000379115; ENSP00000368410; ENSG00000007372. [P26367-2]
Genome annotation databasesEnsembl ENST00000379123; ENSP00000368418; ENSG00000007372. [P26367-1]
Genome annotation databasesEnsembl ENST00000379129; ENSP00000368424; ENSG00000007372. [P26367-2]
Genome annotation databasesEnsembl ENST00000379132; ENSP00000368427; ENSG00000007372. [P26367-1]
Genome annotation databasesEnsembl ENST00000419022; ENSP00000404100; ENSG00000007372. [P26367-2]
Genome annotation databasesEnsembl ENST00000606377; ENSP00000480026; ENSG00000007372. [P26367-2]
Genome annotation databasesGeneID 5080; -.
Genome annotation databasesKEGG hsa:5080; -.
Genome annotation databasesUCSC uc001mtd.4; human. [P26367-1]
Sequence databasesCCDS CCDS31451.1; -. [P26367-1]
Sequence databasesCCDS CCDS31452.1; -. [P26367-2]
Sequence databasesEMBL M77844; AAA59962.1; -; mRNA.
Sequence databasesEMBL M93650; AAA36416.1; -; mRNA.
Sequence databasesEMBL AY047583; AAK95849.1; -; mRNA.
Sequence databasesEMBL BX640762; CAE45868.1; -; mRNA.
Sequence databasesEMBL Z95332; CAG38363.1; -; Genomic_DNA.
Sequence databasesEMBL Z83307; CAG38363.1; JOINED; Genomic_DNA.
Sequence databasesEMBL Z83307; CAG38087.1; -; Genomic_DNA.
Sequence databasesEMBL Z95332; CAG38087.1; JOINED; Genomic_DNA.
Sequence databasesEMBL BC011953; AAH11953.1; -; mRNA.
Sequence databasesPIR A56674; A56674.
Sequence databasesRefSeq NP_000271.1; NM_000280.4. [P26367-1]
Sequence databasesRefSeq NP_001121084.1; NM_001127612.1. [P26367-1]
Sequence databasesRefSeq NP_001245393.1; NM_001258464.1. [P26367-1]
Sequence databasesRefSeq NP_001245394.1; NM_001258465.1. [P26367-1]
Sequence databasesRefSeq NP_001595.2; NM_001604.5. [P26367-2]
Sequence databasesRefSeq XP_005253012.1; XM_005252955.2. [P26367-1]
Sequence databasesRefSeq XP_005253013.1; XM_005252956.2. [P26367-1]
Sequence databasesUniGene Hs.270303; -.
Sequence databasesUniGene Hs.611376; -.
Polymorphism databasesDMDM 6174889; -.
Gene expression databasesBgee P26367; -.
Gene expression databasesCleanEx HS_PAX6; -.
Gene expression databasesExpressionAtlas P26367; baseline and differential.
Gene expression databasesGenevestigator P26367; -.
OntologiesGO GO:0005737; C:cytoplasm; IDA:UniProtKB.
OntologiesGO GO:0000790; C:nuclear chromatin; IDA:BHF-UCL.
OntologiesGO GO:0005634; C:nucleus; IDA:UniProtKB.
OntologiesGO GO:0003680; F:AT DNA binding; IEA:Ensembl.
OntologiesGO GO:0003682; F:chromatin binding; IEA:Ensembl.
OntologiesGO GO:0003677; F:DNA binding; TAS:ProtInc.
OntologiesGO GO:0003690; F:double-stranded DNA binding; IEA:Ensembl.
OntologiesGO GO:0035035; F:histone acetyltransferase binding; ISS:BHF-UCL.
OntologiesGO GO:0019901; F:protein kinase binding; ISS:BHF-UCL.
OntologiesGO GO:0070412; F:R-SMAD binding; IPI:BHF-UCL.
OntologiesGO GO:0000978; F:RNA polymerase II core promoter proximal region sequence-specific DNA binding; IEA:Ensembl.
OntologiesGO GO:0001077; F:RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription; IEA:Ensembl.
OntologiesGO GO:0000979; F:RNA polymerase II core promoter sequence-specific DNA binding; IDA:BHF-UCL.
OntologiesGO GO:0000981; F:sequence-specific DNA binding RNA polymerase II transcription factor activity; IDA:BHF-UCL.
OntologiesGO GO:0003700; F:sequence-specific DNA binding transcription factor activity; TAS:ProtInc.
OntologiesGO GO:0008134; F:transcription factor binding; ISS:BHF-UCL.
OntologiesGO GO:0004842; F:ubiquitin-protein transferase activity; ISS:UniProtKB.
OntologiesGO GO:0048708; P:astrocyte differentiation; IEA:Ensembl.
OntologiesGO GO:0007411; P:axon guidance; IEA:Ensembl.
OntologiesGO GO:0001568; P:blood vessel development; IMP:DFLAT.
OntologiesGO GO:0001709; P:cell fate determination; IEA:Ensembl.
OntologiesGO GO:0007417; P:central nervous system development; TAS:ProtInc.
OntologiesGO GO:0021796; P:cerebral cortex regionalization; IEA:Ensembl.
OntologiesGO GO:0021902; P:commitment of neuronal cell to specific neuron type in forebrain; IEA:Ensembl.
OntologiesGO GO:0061303; P:cornea development in camera-type eye; IMP:DFLAT.
OntologiesGO GO:0009950; P:dorsal/ventral axis specification; IEA:Ensembl.
OntologiesGO GO:0048596; P:embryonic camera-type eye morphogenesis; IEA:Ensembl.
OntologiesGO GO:0001654; P:eye development; TAS:ProtInc.
OntologiesGO GO:0042462; P:eye photoreceptor cell development; IEA:Ensembl.
OntologiesGO GO:0021797; P:forebrain anterior/posterior pattern specification; IEA:Ensembl.
OntologiesGO GO:0021798; P:forebrain dorsal/ventral pattern formation; IEA:Ensembl.
OntologiesGO GO:0021905; P:forebrain-midbrain boundary formation; IEA:Ensembl.
OntologiesGO GO:0042593; P:glucose homeostasis; IMP:DFLAT.
OntologiesGO GO:0030902; P:hindbrain development; IEA:Ensembl.
OntologiesGO GO:0061072; P:iris morphogenesis; IMP:DFLAT.
OntologiesGO GO:0030216; P:keratinocyte differentiation; IEA:Ensembl.
OntologiesGO GO:0032808; P:lacrimal gland development; IEA:Ensembl.
OntologiesGO GO:0002088; P:lens development in camera-type eye; IEA:Ensembl.
OntologiesGO GO:0050680; P:negative regulation of epithelial cell proliferation; IEA:Ensembl.
OntologiesGO GO:0050768; P:negative regulation of neurogenesis; ISS:UniProtKB.
OntologiesGO GO:0045665; P:negative regulation of neuron differentiation; IEA:Ensembl.
OntologiesGO GO:0048663; P:neuron fate commitment; NAS:UniProtKB.
OntologiesGO GO:0001764; P:neuron migration; IEA:Ensembl.
OntologiesGO GO:0021778; P:oligodendrocyte cell fate specification; IEA:Ensembl.
OntologiesGO GO:0009887; P:organ morphogenesis; TAS:ProtInc.
OntologiesGO GO:0003322; P:pancreatic A cell development; IMP:BHF-UCL.
OntologiesGO GO:0021983; P:pituitary gland development; IEA:Ensembl.
OntologiesGO GO:0042660; P:positive regulation of cell fate specification; IEA:Ensembl.
OntologiesGO GO:0030858; P:positive regulation of epithelial cell differentiation; IEA:Ensembl.
OntologiesGO GO:0010628; P:positive regulation of gene expression; IMP:BHF-UCL.
OntologiesGO GO:0002052; P:positive regulation of neuroblast proliferation; IEA:Ensembl.
OntologiesGO GO:0045944; P:positive regulation of transcription from RNA polymerase II promoter; ISS:BHF-UCL.
OntologiesGO GO:0045893; P:positive regulation of transcription, DNA-templated; IMP:BHF-UCL.
OntologiesGO GO:0033365; P:protein localization to organelle; IEA:Ensembl.
OntologiesGO GO:0016567; P:protein ubiquitination; ISS:GOC.
OntologiesGO GO:0030334; P:regulation of cell migration; IEA:Ensembl.
OntologiesGO GO:0048505; P:regulation of timing of cell differentiation; IEA:Ensembl.
OntologiesGO GO:0021918; P:regulation of transcription from RNA polymerase II promoter involved in somatic motor neuron fate commitment; IEA:Ensembl.
OntologiesGO GO:0021912; P:regulation of transcription from RNA polymerase II promoter involved in spinal cord motor neuron fate specification; IEA:Ensembl.
OntologiesGO GO:0021913; P:regulation of transcription from RNA polymerase II promoter involved in ventral spinal cord interneuron specification; IEA:Ensembl.
OntologiesGO GO:0009611; P:response to wounding; IEP:UniProtKB.
OntologiesGO GO:0060041; P:retina development in camera-type eye; IEA:Ensembl.
OntologiesGO GO:0007435; P:salivary gland morphogenesis; IEA:Ensembl.
OntologiesGO GO:0023019; P:signal transduction involved in regulation of gene expression; IEA:Ensembl.
OntologiesGO GO:0007224; P:smoothened signaling pathway; IEA:Ensembl.
OntologiesGO GO:0006366; P:transcription from RNA polymerase II promoter; IMP:BHF-UCL.
OntologiesGO GO:0003309; P:type B pancreatic cell differentiation; IEA:Ensembl.
OntologiesGO GO:0007601; P:visual perception; TAS:ProtInc.
Proteomic databasesMaxQB P26367; -.
Proteomic databasesPaxDb P26367; -.
Proteomic databasesPRIDE P26367; -.
Family and domain databasesGene3D 1.10.10.10; -; 2.
Family and domain databasesGene3D 1.10.10.60; -; 1.
Family and domain databasesInterPro IPR017970; Homeobox_CS.
Family and domain databasesInterPro IPR001356; Homeobox_dom.
Family and domain databasesInterPro IPR009057; Homeodomain-like.
Family and domain databasesInterPro IPR001523; Paired_dom.
Family and domain databasesInterPro IPR011991; WHTH_DNA-bd_dom.
Family and domain databasesPfam PF00046; Homeobox; 1.
Family and domain databasesPfam PF00292; PAX; 1.
Family and domain databasesPRINTS PR00027; PAIREDBOX.
Family and domain databasesPROSITE PS00027; HOMEOBOX_1; 1.
Family and domain databasesPROSITE PS50071; HOMEOBOX_2; 1.
Family and domain databasesPROSITE PS00034; PAIRED_1; 1.
Family and domain databasesPROSITE PS51057; PAIRED_2; 1.
Family and domain databasesSMART SM00389; HOX; 1.
Family and domain databasesSMART SM00351; PAX; 1.
Family and domain databasesSUPFAM SSF46689; SSF46689; 2.
PTM databasesPhosphoSite P26367; -.
Protein-protein interaction databasesBioGrid 111114; 31.
Protein-protein interaction databasesDIP DIP-37436N; -.
Protein-protein interaction databasesIntAct P26367; 6.
Protein-protein interaction databasesMINT MINT-1465118; -.
Protein-protein interaction databasesSTRING 9606.ENSP00000368401; -.
Enzyme and pathway databasesReactome REACT_13819; Regulation of gene expression in beta cells.
Enzyme and pathway databasesReactome REACT_23824; Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP).
Enzyme and pathway databasesReactome REACT_24019; Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1).
Enzyme and pathway databasesSignaLink P26367; -.
3D structure databasesPDB 2CUE; NMR; -; A=211-277.
3D structure databasesPDB 6PAX; X-ray; 2.50 A; A=4-136.
3D structure databasesPDBsum 2CUE; -.
3D structure databasesPDBsum 6PAX; -.
3D structure databasesProteinModelPortal P26367; -.
3D structure databasesSMR P26367; 4-136, 211-278.
Protocols and materials databasesDNASU 5080; -.
Phylogenomic databaseseggNOG NOG326044; -.
Phylogenomic databasesGeneTree ENSGT00680000099553; -.
Phylogenomic databasesHOVERGEN HBG009115; -.
Phylogenomic databasesInParanoid P26367; -.
Phylogenomic databasesKO K08031; -.
Phylogenomic databasesOMA AGENTNS; -.
Phylogenomic databasesOrthoDB EOG7WT431; -.
Phylogenomic databasesPhylomeDB P26367; -.
Phylogenomic databasesTreeFam TF320146; -.
Organism-specific databasesCTD 5080; -.
Organism-specific databasesGeneCards GC11M031806; -.
Organism-specific databasesGeneReviews PAX6; -.
Organism-specific databasesHGNC HGNC:8620; PAX6.
Organism-specific databasesHPA CAB034143; -.
Organism-specific databasesHPA HPA030775; -.
Organism-specific databasesMIM 106210; phenotype.
Organism-specific databasesMIM 120200; phenotype.
Organism-specific databasesMIM 120430; phenotype.
Organism-specific databasesMIM 136520; phenotype.
Organism-specific databasesMIM 148190; phenotype.
Organism-specific databasesMIM 165550; phenotype.
Organism-specific databasesMIM 206700; phenotype.
Organism-specific databasesMIM 604229; phenotype.
Organism-specific databasesMIM 607108; gene.
Organism-specific databasesneXtProt NX_P26367; -.
Organism-specific databasesOrphanet 1065; Aniridia - cerebellar ataxia - intellectual disability.
Organism-specific databasesOrphanet 2334; Autosomal dominant keratitis.
Organism-specific databasesOrphanet 2253; Foveal hypoplasia - presenile cataract.
Organism-specific databasesOrphanet 250923; Isolated aniridia.
Organism-specific databasesOrphanet 137902; Isolated optic nerve hypoplasia.
Organism-specific databasesOrphanet 35737; Morning glory syndrome.
Organism-specific databasesOrphanet 194; Ocular coloboma.
Organism-specific databasesOrphanet 708; Peters anomaly.
Organism-specific databasesOrphanet 893; WAGR syndrome.
Organism-specific databasesPharmGKB PA32960; -.
OtherChiTaRS PAX6; human.
OtherEvolutionaryTrace P26367; -.
OtherGeneWiki PAX6; -.
OtherGenomeRNAi 5080; -.
OtherNextBio 19596; -.
OtherPRO PR:P26367; -.



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