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 **17601 - 17625** 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
Q9BU23	Lipase maturation factor 2	LMF2 TMEM112B TMEM153	Homo sapiens (human)	3	9
Q14571	Inositol 1,4,5-trisphosphate receptor type 2	ITPR2	Homo sapiens (human)	4	9
P48551	Interferon alpha/beta receptor 2	IFNAR2 IFNABR IFNARB	Homo sapiens (human)	6	9
Q9H5K3	Protein O-mannose kinase	POMK SGK196	Homo sapiens (human)	5	9	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome 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 bilateral optic nerve hypoplasia blindness cardiomyopathy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopia 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
O43405	Cochlin	COCH COCH5B2	Homo sapiens (human)	8	9
P02656	Apolipoprotein C-III	APOC3	Homo sapiens (human)	3	9
P20827	Ephrin-A1	EFNA1 EPLG1 LERK1 TNFAIP4	Homo sapiens (human)	4	9	acute myocardial infarction adenocarcinoma adenoma allergic asthma arteriovenous malformation asthma benign giant cell tumor bladder carcinoma bone osteosarcoma botryoid rhabdomyosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary thrombosis cribriform carcinoma diabetic ketoacidosis distal arthrogryposis embryoma embryonal rhabdomyosarcoma esophagus squamous cell carcinoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma intestinal benign neoplasm intestinal cancer intrinsic asthma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma malignant pleural mesothelioma melanoma mixed glioma myocardial infarction nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 osteosarcoma ovarian cancer ovarian carcinoma papillary renal cell carcinoma pre-eclampsia primary pulmonary hypertension renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma transitional cell carcinoma 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 urinary bladder cancer
Q6X4U4	Sclerostin domain-containing protein 1	SOSTDC1 USAG1	Homo sapiens (human)	2	9
Q7Z739	YTH domain-containing family protein 3	YTHDF3	Homo sapiens (human)	18	9
P98161	Polycystin-1	PKD1	Homo sapiens (human)	60	9	Alzheimer's disease Caroli disease Creutzfeldt-Jakob disease Duchenne muscular dystrophy Guillain-Barre syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome Moyamoya disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Streptococcus pneumonia Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute interstitial pneumonia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia anaplastic astrocytoma angiomyolipoma arteriosclerotic cardiovascular disease atherosclerosis autoimmune pancreatitis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease azoospermia bacterial sepsis bone disease bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer cardiomyopathy cartilage disease cavernous hemangioma central nervous system cancer childhood cerebral astrocytoma chorioangioma chronic kidney disease clear cell renal cell carcinoma collagen disease colorectal cancer colorectal carcinoma congenital heart disease congestive heart failure connective tissue disease coronary artery disease coronary thrombosis cutaneous fibrous histiocytoma cystic fibrosis cystic kidney disease dermoid cyst dextrocardia diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma endomyocardial fibrosis epilepsy episodic kinesigenic dyskinesia 1 essential hypertension familial hypertrophic cardiomyopathy familial nephrotic syndrome fibrillary astrocytoma focal segmental glomerulosclerosis gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor growth hormone secreting pituitary adenoma hemangioma hemoglobin H disease hidradenoma high grade glioma histiocytoid hemangioma hyperinsulinism hypertension hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis influenza insulinoma intracranial aneurysm intramuscular hemangioma isolated elevated serum creatine phosphokinase levels juvenile pilocytic astrocytoma keratosis follicularis kidney cancer kidney disease kidney failure large intestine cancer lipoid nephrosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioma lymphopenia malignant astrocytoma melanoma mesangial proliferative glomerulonephritis mixed glioma mongolian spot muscular dystrophy myocardial infarction nephritis nephrolithiasis nephrosis nephrotic syndrome neurofibromatosis 1 neurofibromatosis neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis non-congenital cyst of kidney nutmeg liver obesity osteosarcoma pancreatic cancer pancreatic carcinoma papilloma parapsoriasis pilocytic astrocytoma pneumonia polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease 4 polycystic liver disease polycystic ovary syndrome prostate cancer prostate carcinoma protoplasmic astrocytoma pseudoxanthoma elasticum psoriasis pustulosis of palm and sole pyoureter red color blindness renal carcinoma renal cell carcinoma renovascular hypertension rheumatoid arthritis silent myocardial infarction situs inversus skin melanoma skin papilloma skin tag squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma syringoma thalassemia thoracic aortic aneurysm thyroid gland anaplastic carcinoma tuberous sclerosis 1 tuberous sclerosis 2 tuberous sclerosis type 2 diabetes mellitus uremia uric acid nephrolithiasis visual epilepsy
Q6ZMG9	Ceramide synthase 6	CERS6 LASS6	Homo sapiens (human)	1	9	Kawasaki disease Kennedy's disease T-cell acute lymphoblastic leukemia acute lymphoblastic leukemia adult acute lymphocytic leukemia alcoholic hepatitis alcoholic liver cirrhosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood acute lymphocytic leukemia chronic fatigue syndrome colitis colorectal cancer colorectal carcinoma diabetes mellitus disease of metabolism embryoma encephalitis encephalomyelitis gastroenteritis glucose intolerance head and neck squamous cell carcinoma hematologic cancer idiopathic scoliosis ileitis ileocolitis large intestine cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma mitochondrial metabolism disease mitochondrial myopathy multiple sclerosis myelitis obesity prediabetes syndrome skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder tongue squamous cell carcinoma type 2 diabetes mellitus
Q96A83	Collagen alpha-1(XXVI) chain	COL26A1 EMID2 EMU2	Homo sapiens (human)	8	9
P01374	Lymphotoxin-alpha	LTA TNFB TNFSF1	Homo sapiens (human)	2	10
Q92508	Piezo-type mechanosensitive ion channel component 1	PIEZO1 FAM38A KIAA0233	Homo sapiens (human)	3	10
P04839	Cytochrome b-245 heavy chain	CYBB NOX2	Homo sapiens (human)	7	10
P54760	Ephrin type-B receptor 4	EPHB4 HTK MYK1 TYRO11	Homo sapiens (human)	4	10
Q58EX2	Protein sidekick-2	SDK2 KIAA1514	Homo sapiens (human)	15	10
P19883	Follistatin	FST	Homo sapiens (human)	4	10
Q9H0V9	VIP36-like protein	LMAN2L VIPL	Homo sapiens (human)	3	10	agnosia attention deficit hyperactivity disorder bipolar disorder borderline personality disorder cerebral degeneration choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy intermittent explosive disorder lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary adenocarcinoma papillary renal cell carcinoma partial motor epilepsy pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 thyroid gland papillary carcinoma visual epilepsy
O75369	Filamin-B	FLNB FLN1L FLN3 TABP TAP	Homo sapiens (human)	12	10
Q14703	Membrane-bound transcription factor site-1 protease	MBTPS1 KIAA0091 S1P SKI1	Homo sapiens (human)	16	10
Q9BX74	TM2 domain-containing protein 1	TM2D1 BBP	Homo sapiens (human)	5	10
Q02083	N-acylethanolamine-hydrolyzing acid amidase	NAAA ASAHL PLT	Homo sapiens (human)	6	10	Alagille syndrome 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 Burkitt lymphoma DiGeorge syndrome Glanzmann's thrombasthenia Goodpasture syndrome Hantavirus hemorrhagic fever with renal syndrome Henoch-Schoenlein purpura 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 Japanese encephalitis Marfan syndrome Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Takayasu's arteritis abdominal obesity-metabolic syndrome 1 acrodermatitis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia adult acute lymphocytic leukemia adult respiratory distress syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis bacterial sepsis bladder carcinoma blood coagulation disease bone marrow cancer cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia colorectal cancer colorectal carcinoma coronary artery disease craniosynostosis dengue disease dermatitis diabetes mellitus diabetic ketoacidosis embryoma essential thrombocythemia granulomatosis with polyangiitis gray platelet syndrome heart disease hemophagocytic lymphohistiocytosis hepatitis C hepatocellular carcinoma hypersensitivity vasculitis inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer leukopenia liver cancer liver cirrhosis macrocytic anemia myelodysplastic syndrome myeloproliferative neoplasm newborn respiratory distress syndrome nicotine dependence obesity obsolete inherited blood coagulation disease obsolete type 1 diabetes mellitus 9 osteoarthritis platelet-type bleeding disorder 10 platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 pneumonia polyarteritis nodosa portal hypertension portal vein thrombosis primary pulmonary hypertension prostate cancer prostate carcinoma qualitative platelet defect situs inversus steatotic liver disease thalassemia thrombocytopenia thrombocytosis tuberous sclerosis 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 velocardiofacial syndrome viral infectious disease yellow fever
Q9NXG6	Transmembrane prolyl 4-hydroxylase	P4HTM PH4	Homo sapiens (human)	6	10
P31997	Carcinoembryonic antigen-related cell adhesion molecule 8	CEACAM8 CGM6	Homo sapiens (human)	11	10

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