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 **16876 - 16900** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q504Y2	Extracellular tyrosine-protein kinase PKDCC	PKDCC SGK493 VLK	Homo sapiens (human)	7	4
P51884	Lumican	LUM LDC SLRR2D	Homo sapiens (human)	7	297
Q9Y3Q0	N-acetylated-alpha-linked acidic dipeptidase 2	NAALAD2	Homo sapiens (human)	7	7
Q9P219	Protein Daple	CCDC88C DAPLE KIAA1509	Homo sapiens (human)	7	1
P31327	Carbamoyl-phosphate synthase [ammonia], mitochondrial	CPS1	Homo sapiens (human)	7	5
P06865	Beta-hexosaminidase subunit alpha	HEXA	Homo sapiens (human)	7	27	GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Sandhoff disease Tay-Sachs disease Werdnig-Hoffmann disease acquired immunodeficiency syndrome adult lymphoma amyotrophic lateral sclerosis blindness cancer central nervous system cancer central nervous system lymphoma childhood lymphoma childhood spinal muscular atrophy cystic fibrosis dementia diffuse scleroderma embryoma epilepsy gangliosidosis gliosarcoma glycoproteinosis high grade glioma human immunodeficiency virus infectious disease inherited metabolic disorder intellectual disability juvenile spinal muscular atrophy learning disability lingual-facial-buccal dyskinesia lymphoma lysosomal storage disease mixed glioma movement disease mucolipidosis type IV neurodegenerative disease obesity obsolete ymphosarcoma progressive muscular atrophy rheumatoid arthritis sensorineural hearing loss sickle cell anemia spinal muscular atrophy visual epilepsy
O95631	Netrin-1	NTN1 NTN1L	Homo sapiens (human)	7	4
P54253	Ataxin-1	ATXN1 ATX1 SCA1	Homo sapiens (human)	7	1
P22891	Vitamin K-dependent protein Z	PROZ	Homo sapiens (human)	7	3
Q9H324	A disintegrin and metalloproteinase with thrombospondin motifs 10	ADAMTS10	Homo sapiens (human)	7	3
Q8NI27	THO complex subunit 2	THOC2 CXorf3	Homo sapiens (human)	7	1
Q9NZJ5	Eukaryotic translation initiation factor 2-alpha kinase 3	EIF2AK3 PEK PERK	Homo sapiens (human)	7	3
P25705	ATP synthase subunit alpha, mitochondrial	ATP5F1A ATP5A ATP5A1 ATP5AL2 ATPM	Homo sapiens (human)	7	1
Q13469	Nuclear factor of activated T-cells, cytoplasmic 2	NFATC2 NFAT1 NFATP	Homo sapiens (human)	7	2
O00443	Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha	PIK3C2A	Homo sapiens (human)	7	1	Duchenne muscular dystrophy Gamstorp-Wohlfart syndrome Kaposi's sarcoma Laron syndrome Norum disease Tangier disease Unverricht-Lundborg syndrome abetalipoproteinemia achondroplasia acquired immunodeficiency syndrome acute myocardial infarction anodontia arteriosclerotic cardiovascular disease atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative 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 blepharospasm breast cancer breast carcinoma cancer choreaacanthocytosis chronic monocytic leukemia congenital hypothyroidism congenital muscular dystrophy coronary artery disease coronary thrombosis cryptorchidism diabetes mellitus disease of mental health distal myopathy early myoclonic encephalopathy embryoma episodic ataxia type 1 facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia focal hand dystonia gastrointestinal stromal tumor glaucoma hypercalcemia hyperphosphatemia hypolipoproteinemia hypothyroidism leukopenia limb-girdle muscular dystrophy lymphoid leukemia muscular dystrophy myeloid leukemia myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis myotonic dystrophy type 2 myxedema nephrocalcinosis neuroleptic malignant syndrome nutmeg liver 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 phosphorus metabolism disease placental insufficiency protein-losing enteropathy psychotic disorder rippling muscle disease 2 schizoaffective disorder schizophrenia schizophreniform disorder scoliosis sensorineural hearing loss silent myocardial infarction systemic lupus erythematosus thrombocytopenia tibial muscular dystrophy tooth agenesis type 2 diabetes mellitus
Q02809	Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1	PLOD1 LLH PLOD	Homo sapiens (human)	7	57	Ehlers-Danlos syndrome kyphoscoliotic type 1 brittle cornea syndrome 1
P19256	Lymphocyte function-associated antigen 3	CD58 LFA3	Homo sapiens (human)	7	8
Q8WUA8	Tsukushi	TSKU E2IG4 LRRC54 TSK	Homo sapiens (human)	7	1
Q7L1S5	Carbohydrate sulfotransferase 9	CHST9	Homo sapiens (human)	7	5	acute lymphoblastic leukemia acute myeloid leukemia breast cancer breast carcinoma cancer coronary artery disease depressive disorder essential thrombocythemia hematologic cancer idiopathic scoliosis lymphoblastic lymphoma major depressive disorder melancholic depression myelodysplastic syndrome obsolete melancholia schizophrenia
Q96AE7	Tetratricopeptide repeat protein 17	TTC17	Homo sapiens (human)	7	13
Q8IZL8	Proline-, glutamic acid- and leucine-rich protein 1	PELP1 HMX3 MNAR	Homo sapiens (human)	7	2
P13497	Bone morphogenetic protein 1	BMP1 PCOLC	Homo sapiens (human)	7	14
P49327	Fatty acid synthase	FASN FAS	Homo sapiens (human)	7	4	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 Japanese encephalitis Marinesco-Sjogren syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome X-linked dilated cardiomyopathy Zollinger-Ellison syndrome acoustic neuroma acute chest syndrome adenocarcinoma adenoma adrenal gland hyperfunction adult liposarcoma adult oligodendroglioma agnosia angiomatous meningioma arrhythmogenic right ventricular cardiomyopathy arthritis arthropathy autoimmune lymphoproliferative syndrome bacterial sepsis basal cell carcinoma benign breast phyllodes tumor benign meningioma bladder carcinoma blindness bone cancer bone osteosarcoma brain cancer breast cancer breast carcinoma breast malignant phyllodes tumor bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cerebral convexity meningioma cerebral degeneration chikungunya childhood liposarcoma childhood oligodendroglioma childhood osteosarcoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia clear cell meningioma clear cell renal cell carcinoma clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congenital hypothyroidism congestive heart failure cribriform carcinoma dedifferentiated liposarcoma dengue disease dengue hemorrhagic fever depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1A 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 disease of metabolism dysplastic nevus syndrome embryoma encephalitis encephalomyelitis endometrial adenocarcinoma endometrial cancer endometrial carcinoma endomyocardial fibrosis epithelioid leiomyosarcoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial retinoblastoma fibrous meningioma fundus albipunctatus gastric adenocarcinoma gastrointestinal stromal tumor gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma granular cell tumor head and neck cancer hepatitis B hepatitis C hepatocellular carcinoma herpes simplex high grade glioma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypothyroidism idiopathic interstitial pneumonia inflammatory bowel disease 1 inflammatory bowel disease inflammatory liposarcoma intellectual disability intraorbital meningioma intraventricular meningioma kidney cancer large intestine cancer learning disability leiomyoma leiomyosarcoma leukemia leukopenia liposarcoma liver cancer liver carcinoma luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma mantle cell lymphoma melanoma meningioma meningothelial meningioma microcystic meningioma microinvasive gastric cancer microphthalmia mixed glioma mixed oligodendroglioma-astrocytoma multiple myeloma myelitis myofibroma myotonic dystrophy type 1 myotonic dystrophy type 2 myxedema myxoid leiomyosarcoma nasopharynx carcinoma neurofibromatosis obesity obsolete Cushing's syndrome obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ocular cancer olfactory groove meningioma oligodendroglioma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma pleomorphic adenoma carcinoma pleomorphic adenoma pleomorphic liposarcoma polycystic kidney disease 3 postinflammatory pulmonary fibrosis primary cerebellar degeneration primary hyperaldosteronism primary immunodeficiency disease prostate adenocarcinoma prostate cancer prostate carcinoma psammomatous meningioma pulmonary fibrosis renal carcinoma renal cell carcinoma renal osteodystrophy retinitis pigmentosa retinoblastoma rippling muscle disease 2 sarcomatoid carcinoma sclerosing liposarcoma sebaceous carcinoma secretory meningioma skin melanoma speech-language disorder-1 spinal meningioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma sweat gland cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma transitional meningioma 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 urinary bladder cancer uterine corpus cancer uterine fibroid varicocele vestibular schwannomatosis viral infectious disease well-differentiated liposarcoma yellow fever
Q9NQ79	Cartilage acidic protein 1	CRTAC1 ASPIC1 CEP68	Homo sapiens (human)	7	3
Q9UBX5	Fibulin-5	FBLN5 DANCE	Homo sapiens (human)	7	85

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