GlyCosmos Portal

Displaying entries **6301 - 6325** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
O60673	DNA polymerase zeta catalytic subunit	REV3L POLZ REV3	2	1
O60674	Tyrosine-protein kinase JAK2	JAK2	0	1
O60675	Transcription factor MafK	MAFK	12	2
O60676	Cystatin-8	CST8 CRES	2	0
O60678	Protein arginine N-methyltransferase 3	PRMT3 HRMT1L3	0	1
O60682	Musculin	MSC ABF1 BHLHA22	0	1
O60684	Importin subunit alpha-7	KPNA6 IPOA7	0	1
O60687	Sushi repeat-containing protein SRPX2	SRPX2 SRPUL	2	1
O60701	UDP-glucose 6-dehydrogenase	UGDH	1	1	Graves' disease Laron syndrome Zollinger-Ellison syndrome achondroplasia beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cholangiocarcinoma diarrhea enophthalmos giant cell glioblastoma giardiasis glioblastoma hepatocellular carcinoma high grade glioma hyperinsulinism hyperthyroidism hypoglycemia intrahepatic cholangiocarcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma obsolete exophthalmos orbital disease peripheral artery disease placental insufficiency primary hyperoxaluria thalassemia thyrotoxicosis
O60704	Protein-tyrosine sulfotransferase 2	TPST2	10	3
O60706	ATP-binding cassette sub-family C member 9	ABCC9 SUR2	6	1
O60716	Catenin delta-1	CTNND1 KIAA0384	2	5
O60721	Sodium/potassium/calcium exchanger 1	SLC24A1 KIAA0702 NCKX1	1	0
O60732	Melanoma-associated antigen C1	MAGEC1	0	1
O60739	Eukaryotic translation initiation factor 1b	EIF1B	0	1
O60741	Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1	HCN1 BCNG1	4	1
O60749	Sorting nexin-2	SNX2	1	1
O60755	Galanin receptor type 3	GALR3 GALNR3	1	0
O60760	Hematopoietic prostaglandin D synthase	HPGDS GSTS PGDS PTGDS2	1	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 B-cell lymphoma Barrett's esophagus Bell's palsy Burkitt lymphoma Crohn's colitis Crohn's disease Down syndrome Duchenne muscular dystrophy Fanconi anemia complementation group A Fanconi anemia Friedreich ataxia 1 Friedreich ataxia Gilles de la Tourette syndrome HELLP syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kuhnt-Junius degeneration Langerhans-cell histiocytosis Loeffler syndrome Lyme disease Meniere's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium vivax malaria Reye syndrome Richter's syndrome Sertoli cell-only syndrome T-cell acute lymphoblastic leukemia X-linked ichthyosis X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 Y-linked spermatogenic failure 1 Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acquired immunodeficiency syndrome acrodermatitis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma adult medulloblastoma adult respiratory distress syndrome age related macular degeneration alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis allergic asthma alopecia alternating hemiplegia of childhood amyotrophic lateral sclerosis anaplastic astrocytoma androgenic alopecia angioedema angiomatous meningioma anthracosilicosis aortic valve insufficiency aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autism spectrum disorder autistic disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant cerebellar ataxia autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy azoospermia basal cell carcinoma benign meningioma benign mesothelioma beta thalassemia bipolar disorder bladder carcinoma bladder urothelial carcinoma bone cancer bone osteosarcoma brain cancer brain disease brain stem infarction breast cancer breast carcinoma breast ductal carcinoma bronchiolo-alveolar adenocarcinoma bronchitis bronchus cancer bronchus carcinoma byssinosis cancer carcinoma cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease cataract celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral artery occlusion cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood acute myeloid leukemia childhood cerebral astrocytoma childhood disintegrative disease childhood leukemia childhood lymphoma childhood medulloblastoma childhood osteosarcoma childhood testicular germ cell tumor chromophobe renal cell carcinoma chronic ethmoiditis chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital heart disease congenital muscular dystrophy congestive heart failure coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma cryptorchidism cystic fibrosis cystinuria degeneration of macula and posterior pole dementia dental fluorosis depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diastrophic dysplasia diffuse large B-cell lymphoma distal myopathy drug psychosis dry eye syndrome dysthymic disorder embryoma embryonal cancer encephalitis encephalomyelitis endolymphatic hydrops endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis enterobiasis eosinophilic pneumonia epilepsy esophageal cancer esophageal carcinoma esophageal disease esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia essential tremor exanthem exanthema subitum exfoliation syndrome exocrine pancreatic insufficiency extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial periodic paralysis familial retinoblastoma fascioliasis female reproductive organ cancer fibrillary astrocytoma fibromyalgia fibrous meningioma fissured tongue follicular adenoma follicular lymphoma galactosemia gallbladder cancer gallbladder carcinoma gallbladder disease gastric adenocarcinoma gastric lymphoma gastritis gastroenteritis gastroesophageal junction adenocarcinoma gastroesophageal reflux disease gastrointestinal system cancer gemistocytic astrocytoma generalized atherosclerosis geographic tongue germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glaucoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hematologic cancer hemochromatosis type 1 hemochromatosis hemolytic anemia hepatitis A hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma hereditary sensory and autonomic neuropathy type 5 heroin dependence high grade glioma human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypothalamic disease idiopathic interstitial pneumonia ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer intestinal schistosomiasis intestinal volvulus intraorbital meningioma intraventricular meningioma intrinsic asthma invasive ductal carcinoma islet cell tumor juvenile pilocytic astrocytoma keratosis follicularis keratosis kidney cancer kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease laryngeal squamous cell carcinoma larynx cancer leiomyoma leukemia leukopenia lichen disease limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoma lymphoplasmacyte-rich meningioma macular degeneration major depressive disorder malaria male infertility malignant astrocytoma malignant mesothelioma mantle cell lymphoma marasmus medulloblastoma medulloepithelioma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma membranous glomerulonephritis meningioma meningothelial meningioma microcystic adenoma microcystic meningioma migraine without aura mixed glioma mongolian spot mood disorder mucoepidermoid carcinoma multiple myeloma multiple sclerosis muscular dystrophy myelitis myelodysplastic syndrome myeloid leukemia myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myofibroma myopathy myositis nasopharynx carcinoma neonatal jaundice neovascular inflammatory vitreoretinopathy nephroblastoma nephrolithiasis nervous system disease neuroblastoma neurodegenerative disease neuroectodermal tumor neuropathy neurotic disorder newborn respiratory distress syndrome nicotine dependence nodular prostate non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy olfactory groove meningioma oligospermia onchocerciasis oral mucosa leukoplakia osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma parathyroid gland disease peptic esophagitis periodontitis peripheral nervous system disease pilocytic astrocytoma pituitary adenoma plasmacytoma pleomorphic adenoma pneumonia polycystic ovary syndrome polycythemia vera polycythemia polyneuropathy porphyria cutanea tarda postinflammatory pulmonary fibrosis pre-eclampsia primary biliary cholangitis primary cutaneous amyloidosis primary open angle glaucoma primary pulmonary hypertension progressive multifocal leukoencephalopathy progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma prostatic adenoma protein-energy malnutrition protoplasmic astrocytoma psammomatous meningioma pseudoxanthoma elasticum psoriasis psychotic disorder pulmonary fibrosis pure red-cell aplasia pustulosis of palm and sole rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease reticulosarcoma retinoblastoma rheumatoid arthritis rhinitis rippling muscle disease 2 rubella sarcomatoid carcinoma sarcomatoid renal cell carcinoma schistosomiasis schizoaffective disorder schizophrenia schizophreniform disorder scleroderma scurvy secondary Parkinson disease secretory meningioma seminoma senile cataract sensorineural hearing loss sialuria sickle cell anemia silent myocardial infarction skin benign neoplasm skin cancer skin carcinoma skin melanoma skin squamous cell carcinoma small intestine adenocarcinoma spinal meningioma spinocerebellar ataxia type 2 sporadic breast cancer squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma stomach disease subependymal giant cell astrocytoma sudden infant death syndrome supratentorial primitive neuroectodermal tumor systemic lupus erythematosus systemic scleroderma tarsal-carpal coalition syndrome testicular cancer testicular germ cell cancer testicular malignant germ cell cancer testis seminoma thalassemia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue disease tongue squamous cell carcinoma tracheal disease transitional cell carcinoma transitional meningioma trichinosis trilateral retinoblastoma tuberculosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ureteral obstruction uric acid nephrolithiasis urinary bladder cancer urticaria uterine corpus cancer uterine fibroid varicocele visual epilepsy vitiligo white sponge nevus xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum xerophthalmia
O60762	Dolichol-phosphate mannosyltransferase subunit 1	DPM1	0	1	Duchenne muscular dystrophy antithrombin III deficiency autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy capillary disease cavernous hemangioma chorioangioma congenital disorder of glycosylation Ie congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy glomus tumor hemangioma hereditary hemorrhagic telangiectasia histiocytoid hemangioma intramuscular hemangioma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lymphangioma microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 nonsyndromic congenital nail disorder 9 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy patent ductus arteriosus protein C deficiency protein S deficiency rippling muscle disease 2 telangiectasis thrombophilia
O60763	General vesicular transport factor p115	USO1 VDP	0	1
O60765	Zinc finger protein 354A	ZNF354A EZNF HKL1 TCF17	0	1
O60779	Thiamine transporter 1	SLC19A2 THT1 TRMA	2	0
O60783	Small ribosomal subunit protein uS14m	MRPS14	0	1
O60812	Heterogeneous nuclear ribonucleoprotein C-like 1	HNRNPCL1 HNRPCL1	0	1

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