GlyCosmos Portal

Source	Last Updated
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 **5451 - 5475** of **126547** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9Y274	Type 2 lactosamine alpha-2,3-sialyltransferase	ST3GAL6 SIAT10	Homo sapiens (human)	7	16	cancer carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer multiple myeloma sarcomatoid carcinoma stomach cancer
Q9Y271	Cysteinyl leukotriene receptor 1	CYSLTR1 CYSLT1	Homo sapiens (human)	4	0
Q9Y267	Solute carrier family 22 member 14	SLC22A14 OCTL2 ORCTL4	Homo sapiens (human)	4	0
Q9Y266	Nuclear migration protein nudC	NUDC	Homo sapiens (human)	0	1
Q9Y265	RuvB-like 1	RUVBL1 INO80H NMP238 TIP49 TIP49A	Homo sapiens (human)	0	1
Q9Y264	Angiopoietin-4	ANGPT4 ANG3 ANG4	Homo sapiens (human)	9	0
Q9Y263	Phospholipase A-2-activating protein	PLAA PLAP	Homo sapiens (human)	1	1
Q9Y262	Eukaryotic translation initiation factor 3 subunit L	EIF3L EIF3EIP EIF3S6IP	Homo sapiens (human)	0	1
Q9Y261	Hepatocyte nuclear factor 3-beta	FOXA2 HNF3B TCF3B	Homo sapiens (human)	0	1
Q9Y259	Choline/ethanolamine kinase	CHKB CHETK CHKL	Homo sapiens (human)	1	1	Balo concentric sclerosis Bell's palsy Duchenne muscular dystrophy X-linked dilated cardiomyopathy adrenoleukodystrophy agnosia 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 bronchus cancer bronchus carcinoma campomelic dysplasia central nervous system disease centronuclear myopathy 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 muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy craniometaphyseal dysplasia cytochrome-c oxidase deficiency disease developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy inherited metabolic disorder isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcolepsy nemaline myopathy 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 recurrent hypersomnia restless legs syndrome rigid spine muscular dystrophy 1 rippling muscle disease 2
Q9Y257	Potassium channel subfamily K member 6	KCNK6 TOSS TWIK2	Homo sapiens (human)	2	0
Q9Y255	PRELI domain-containing protein 1, mitochondrial	PRELID1 PRELI	Homo sapiens (human)	0	1
Q9Y253	DNA polymerase eta	POLH RAD30 RAD30A XPV	Homo sapiens (human)	2	1
Q9Y251	Heparanase	HPSE HEP HPA HPA1 HPR1 HPSE1 HSE1	Homo sapiens (human)	7	7	46,XY sex reversal 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 Barrett's esophagus Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Crohn's colitis Crohn's disease Evans' syndrome Glanzmann's thrombasthenia Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma IgA glomerulonephritis Japanese encephalitis MHC class II deficiency Pick's disease Reye syndrome Sjogren's syndrome X-linked ichthyosis abdominal aortic aneurysm acrodermatitis acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adenosine deaminase deficiency adrenal gland cancer adult hepatocellular carcinoma adult lymphoma adult medulloblastoma adult oligodendroglioma agenesis of the corpus callosum with peripheral neuropathy ameloblastoma anaplastic astrocytoma anemia antithrombin III deficiency anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura basal cell carcinoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bipolar disorder bladder carcinoma blood coagulation disease blood platelet disease bone marrow cancer bone osteosarcoma botryoid rhabdomyosarcoma brain cancer breast adenocarcinoma breast cancer breast carcinoma breast lymphoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease central nervous system cancer central nervous system lymphoma central retinal vein occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ cherubism childhood cerebral astrocytoma childhood medulloblastoma childhood oligodendroglioma cholangiocarcinoma choriocarcinoma chromophobe renal cell carcinoma chronic ethmoiditis chronic fatigue syndrome chronic kidney disease chronic myeloid leukemia chronic sphenoidal sinusitis clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma corneal disease coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma dengue disease depressive disorder dermatitis dermoid cyst of ovary diabetes mellitus diabetic angiopathy diabetic ketoacidosis duodenum cancer dysthymic disorder embryoma embryonal rhabdomyosarcoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exostosis exudative vitreoretinopathy 1 exudative vitreoretinopathy familial cold autoinflammatory syndrome 1 familial cold autoinflammatory syndrome 4 familial cold autoinflammatory syndrome familial nephrotic syndrome fibrillary astrocytoma focal segmental glomerulosclerosis follicular adenoma gallbladder cancer gallbladder carcinoma gastrointestinal system cancer gemistocytic astrocytoma generalized anxiety disorder giant cell glioblastoma gingival fibromatosis glaucoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma gray platelet syndrome head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hepatic veno-occlusive disease hepatitis B hepatitis C hepatocellular carcinoma hepatoerythropoietic porphyria hereditary multiple exostoses hereditary neuropathy with liability to pressure palsies hidradenoma high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy immune system disease in situ carcinoma inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma invasive ductal carcinoma juvenile pilocytic astrocytoma keratoconjunctivitis sicca keratoconus kidney disease kidney failure large intestine cancer laryngeal squamous cell carcinoma leukemia lipoid nephrosis liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoid leukemia lymphoma macrocytic anemia major depressive disorder malaria malignant astrocytoma malignant mesothelioma malignant pleural mesothelioma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma membranous glomerulonephritis microcystic adenoma migraine mixed glioma mixed oligodendroglioma-astrocytoma motor peripheral neuropathy mucinous adenocarcinoma multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome myeloid leukemia myeloproliferative neoplasm myocardial infarction myoma nasopharynx carcinoma nephritis nephrosis nephrotic syndrome neuroblastoma neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder nevoid basal cell carcinoma syndrome nodular prostate nonpapillary renal cell carcinoma nutmeg liver obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oligodendroglioma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenocarcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma parapsoriasis periarthritis peripheral nervous system disease pheochromocytoma pilocytic astrocytoma placenta cancer platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 porphyria cutanea tarda primary immunodeficiency disease proliferative diabetic retinopathy prostate cancer prostate carcinoma prostatic adenoma protein C deficiency protein S deficiency proteinuria protoplasmic astrocytoma psoriasis pustulosis of palm and sole qualitative platelet defect rabies renal carcinoma renal cell carcinoma retinal disease retinal vein occlusion retinitis retinopathy of prematurity rhabdomyosarcoma rheumatoid arthritis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma severe combined immunodeficiency silent myocardial infarction skin melanoma skin papilloma skin tag small intestine cancer spindle cell sarcoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma synovial sarcoma syringoma tendinitis thromboangiitis obliterans thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue cancer tongue squamous cell carcinoma 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 urinary bladder cancer urofacial syndrome uterine corpus cancer vascular disease viral infectious disease von Willebrand's disease 1 von Willebrand's disease yellow fever
Q9Y250	Leucine zipper putative tumor suppressor 1	LZTS1 FEZ1	Homo sapiens (human)	0	1
Q9Y248	DNA replication complex GINS protein PSF2	GINS2 PSF2	Homo sapiens (human)	0	1
Q9Y243	RAC-gamma serine/threonine-protein kinase	AKT3 PKBG	Homo sapiens (human)	3	1
Q9Y241	HIG1 domain family member 1A, mitochondrial	HIGD1A HIG1	Homo sapiens (human)	0	1
Q9Y240	C-type lectin domain family 11 member A	CLEC11A CLECSF3 LSLCL SCGF	Homo sapiens (human)	6	7
Q9Y239	Nucleotide-binding oligomerization domain-containing protein 1	NOD1 CARD4	Homo sapiens (human)	0	1
Q9Y237	Peptidyl-prolyl cis-trans isomerase NIMA-interacting 4	PIN4	Homo sapiens (human)	0	1
Q9Y233	cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A	PDE10A	Homo sapiens (human)	0	1
Q9Y232	Chromodomain Y-like protein	CDYL CDYL1	Homo sapiens (human)	1	1
Q9Y231	4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 9	FUT9	Homo sapiens (human)	3	0	bronchus cancer bronchus carcinoma cancer colorectal cancer colorectal carcinoma embryoma hepatocellular carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma malaria
Q9Y230	RuvB-like 2	RUVBL2 INO80J TIP48 TIP49B	Homo sapiens (human)	2	1

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