GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **2851 - 2875** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9NZ32	Actin-related protein 10	ACTR10 ACTR11 ARP10 ARP11	Homo sapiens (human)	1
P69892	Hemoglobin subunit gamma-2	HBG2	Homo sapiens (human)	1
O95361	Tripartite motif-containing protein 16	TRIM16 EBBP	Homo sapiens (human)	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
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
P28072	Proteasome subunit beta type-6	PSMB6 LMPY Y	Homo sapiens (human)	1
Q9NRW3	DNA dC->dU-editing enzyme APOBEC-3C	APOBEC3C APOBEC1L PBI	Homo sapiens (human)	1
O75153	Clustered mitochondria protein homolog	CLUH KIAA0664	Homo sapiens (human)	1
Q96FN5	Kinesin-like protein KIF12	KIF12	Homo sapiens (human)	1
Q9NXC5	GATOR2 complex protein MIOS	MIOS	Homo sapiens (human)	1
Q504Q3	PAN2-PAN3 deadenylation complex catalytic subunit PAN2	PAN2 KIAA0710 USP52	Homo sapiens (human)	1
O75348	V-type proton ATPase subunit G 1	ATP6V1G1 ATP6G ATP6G1 ATP6J	Homo sapiens (human)	1
P49802	Regulator of G-protein signaling 7	RGS7	Homo sapiens (human)	1
Q9Y2B0	Protein canopy homolog 2	CNPY2 MSAP TMEM4 ZSIG9	Homo sapiens (human)	1
B9A064	Immunoglobulin lambda-like polypeptide 5	IGLL5	Homo sapiens (human)	1
Q9Y2P4	Long-chain fatty acid transport protein 6	SLC27A6 ACSVL2 FACVL2 FATP6	Homo sapiens (human)	1
Q86X76	Deaminated glutathione amidase	NIT1	Homo sapiens (human)	1
P51522	Zinc finger protein 83	ZNF83 ZNF816B	Homo sapiens (human)	1
O75947	ATP synthase subunit d, mitochondrial	ATP5PD ATP5H	Homo sapiens (human)	1
Q7Z478	ATP-dependent RNA helicase DHX29	DHX29 DDX29	Homo sapiens (human)	1

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