GlyCosmos Portal

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Displaying entries **8326 - 8350** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9JII6	Aldo-keto reductase family 1 member A1	Akr1a1 Akr1a4	Mus musculus (house mouse)	1
P80314	T-complex protein 1 subunit beta	Cct2 Cctb	Mus musculus (house mouse)	1
O95361	Tripartite motif-containing protein 16	TRIM16 EBBP	Homo sapiens (human)	1
Q9ESL4	Mitogen-activated protein kinase kinase kinase 20	Map3k20 Mltk Zak	Mus musculus (house mouse)	1
Q4J6C6	Prolyl endopeptidase-like	PREPL KIAA0436	Homo sapiens (human)	1
Q04446	1,4-alpha-glucan-branching enzyme	GBE1	Homo sapiens (human)	1	B-cell lymphoma Cauda equina syndrome Fabry disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Guillain-Barre syndrome Noonan syndrome 1 acute myeloid leukemia bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy chronic ulcer of skin chylomicron retention disease congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome cystinuria cytochrome-c oxidase deficiency disease dementia diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis esophagus squamous cell carcinoma familial lipoprotein lipase deficiency familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy idiopathic scoliosis intellectual disability learning disability leukodystrophy lipid storage disease liver disease locked-in syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy melanoma mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy neurogenic bladder obsolete ymphosarcoma ovarian cancer ovarian carcinoma paraplegia polyhydramnios porphyria portal hypertension quadriplegia rigid spine muscular dystrophy 1 skin melanoma
Q4DZ63	Abnormal spindle-like microcephaly-associated protein ASH domain-containing protein	Tc00.1047053507023.220	Trypanosoma cruzi strain CL Brener	1
A0A125YST2	isocitrate dehydrogenase (NADP(+))	TGVEG_313140	Toxoplasma gondii VEG	1
Q3V3Q7	Phosphofurin acidic cluster sorting protein 2	Pacs2 Kiaa0602 Pacs1l	Mus musculus (house mouse)	1
Q4DAX6	RAB GDP dissociation inhibitor alpha	Tc00.1047053506579.110	Trypanosoma cruzi strain CL Brener	1
V5B6R2	Pyridoxal phosphate homeostasis protein	TCDM_08914	Trypanosoma cruzi Dm28c	1
Q8BGK2	Inactive ADP-ribosyltransferase ARH2	Adprhl1 Arh2	Mus musculus (house mouse)	1
Q4CNM5	ATP-dependent Clp protease subunit, heat shock protein 100 (HSP100), putative (Fragment)	Tc00.1047053508665.14	Trypanosoma cruzi strain CL Brener	1
Q9UK53	Inhibitor of growth protein 1	ING1	Homo sapiens (human)	1
Q92754	Transcription factor AP-2 gamma	TFAP2C	Homo sapiens (human)	1
Q8N910	Putative uncharacterized protein PAK6-AS1	PAK6-AS1 C15orf56	Homo sapiens (human)	1
Q08188	Protein-glutamine gamma-glutamyltransferase E	TGM3	Homo sapiens (human)	1
P00491	Purine nucleoside phosphorylase	PNP NP	Homo sapiens (human)	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Chagas disease Evans' syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lesch-Nyhan syndrome MELAS syndrome MHC class II deficiency Nezelof syndrome Omenn syndrome Pick's disease Reye syndrome Richter's syndrome T cell deficiency acute lymphoblastic leukemia adenosine deaminase deficiency adult lymphoma agammaglobulinemia agnosia alternating hemiplegia of childhood anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autonomic neuropathy bladder carcinoma breast cancer breast carcinoma cancer carcinoma carotid artery disease central nervous system disease central nervous system lymphoma central nervous system vasculitis central retinal vein occlusion cerebral degeneration cerebral malaria cerebral palsy childhood acute lymphocytic leukemia childhood lymphoma chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer combined T cell and B cell immunodeficiency coronary artery disease critical illness polyneuropathy cutaneous leishmaniasis cyclic hematopoiesis developmental coordination disorder diabetic cataract diabetic retinopathy disease of metabolism embryoma esophageal cancer esophageal carcinoma fetal erythroblastosis gangliosidosis giant cell glioblastoma glioblastoma granulomatous angiitis head and neck squamous cell carcinoma hematologic cancer hepatocellular carcinoma herpes simplex high grade glioma hyperuricemia immune system disease inflammatory and toxic neuropathy intellectual disability large intestine cancer learning disability liver cancer locked-in syndrome lupus erythematosus lymphoblastic lymphoma lymphoma lymphopenia macrocytic anemia malaria maxillary sinus squamous cell carcinoma melanoma meningoencephalitis molybdenum cofactor deficiency type A monoclonal gammopathy of uncertain significance nervous system disease neuroblastoma neurodegenerative disease neuropathy obsolete T lymphocyte deficiency obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma periodontal disease periodontitis peripheral T-cell lymphoma peripheral nervous system disease phosphoribosylpyrophosphate synthetase superactivity pneumonia polyneuropathy primary immunodeficiency disease prostate cancer prostate carcinoma purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder quadriplegia reflex sympathetic dystrophy retinal vein occlusion sarcomatoid carcinoma severe combined immunodeficiency sinusitis skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy substance abuse substance-related disorder systemic lupus erythematosus thyroid gland medullary carcinoma trypanosomiasis tuberculosis urinary bladder cancer urinary tract obstruction vascular disease
V5BCE1	ABC transporter	TCDM_08331	Trypanosoma cruzi Dm28c	1
F4I4I8	histone acetyltransferase	HAC12	Arabidopsis thaliana (thale cress)	1
P0C0S6	Histone H2A.Z	H2az1 H2afz H2az	Mus musculus (house mouse)	1
A3KGU5	Spectrin alpha, non-erythrocytic 1	Sptan1 Spna2	Mus musculus (house mouse)	1
P28072	Proteasome subunit beta type-6	PSMB6 LMPY Y	Homo sapiens (human)	1
Q3UQ44	Ras GTPase-activating-like protein IQGAP2	Iqgap2	Mus musculus (house mouse)	1
P06151	L-lactate dehydrogenase A chain	Ldha Ldh-1 Ldh1	Mus musculus (house mouse)	1

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