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 **901 - 925** 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
P22304	Iduronate 2-sulfatase	IDS SIDS	Homo sapiens (human)	9	9	Balo concentric sclerosis Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Fabry disease Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Griscelli syndrome Laron syndrome Marfan syndrome Sveinsson chorioretinal atrophy Waardenburg syndrome type 3 X-linked ichthyosis achondroplasia adrenoleukodystrophy agammaglobulinemia allergic asthma alternating hemiplegia of childhood amnestic disorder antiphospholipid syndrome asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer brain disease breast cancer breast carcinoma cancer central nervous system disease centronuclear myopathy X-linked centronuclear myopathy cerebral infarction cerebrovascular disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital adrenal hyperplasia congenital central hypoventilation syndrome congenital ptosis congenital structural myopathy congestive heart failure craniosynostosis cystinuria depressive disorder diarrhea dysthymic disorder embryoma epilepsy fragile X syndrome galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease glycoproteinosis heart valve disease hydrocephalus hypercalcemia hypertrichosis hypoglycemia inguinal hernia intellectual disability intrinsic asthma learning disability lipid storage disease lung benign neoplasm lung carcinoma lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myeloproliferative neoplasm myocarditis myotonic disease myotonic dystrophy type 2 narcolepsy nephrocalcinosis nervous system disease neurotic disorder obsolete intestinal pseudo-obstruction obsolete melancholia obstructive hydrocephalus obstructive sleep apnea ocular albinism with sensorineural deafness oculocutaneous albinism omphalocele optic papillitis osteochondrodysplasia ovarian cancer ovarian carcinoma pancytopenia papilledema paralytic ileus phosphorus metabolism disease post-traumatic stress disorder ptosis retinal edema retrograde amnesia rumination disorder senile degeneration of brain sensorineural hearing loss sick sinus syndrome situs inversus sleep apnea sudden infant death syndrome trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis umbilical hernia visual epilepsy
P15509	Granulocyte-macrophage colony-stimulating factor receptor subunit alpha	CSF2RA CSF2R CSF2RY	Homo sapiens (human)	11	9
Q13508	Ecto-ADP-ribosyltransferase 3	ART3 TMART	Homo sapiens (human)	2	9	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
Q9NXH8	Torsin-4A	TOR4A C9orf167	Homo sapiens (human)	1	9
Q9NTN9	Semaphorin-4G	SEMA4G KIAA1619	Homo sapiens (human)	6	9
Q53F39	Metallophosphoesterase 1	MPPE1 PGAP5	Homo sapiens (human)	1	9	bipolar disorder borderline personality disorder cancer cerebral malaria chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis B hepatitis influenza intermittent explosive disorder malaria melanoma papillary renal cell carcinoma pneumonia renal cell carcinoma sarcomatoid renal cell carcinoma skin melanoma
Q9NU53	Glycoprotein integral membrane protein 1	GINM1 C6orf72	Homo sapiens (human)	14	9
Q99467	CD180 antigen	CD180 LY64 RP105	Homo sapiens (human)	11	9
Q9H4F8	SPARC-related modular calcium-binding protein 1	SMOC1	Homo sapiens (human)	17	9
P20231	Tryptase beta-2	TPSB2 TPS2	Homo sapiens (human)	1	9
Q68CR1	Protein sel-1 homolog 3	SEL1L3 KIAA0746	Homo sapiens (human)	9	9
Q96K49	Transmembrane protein 87B	TMEM87B	Homo sapiens (human)	5	9
P06127	T-cell surface glycoprotein CD5	CD5 LEU1	Homo sapiens (human)	3	9
P08842	Steryl-sulfatase	STS ARSC1	Homo sapiens (human)	4	9	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 Chagas disease Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down syndrome Dubowitz syndrome Evans' 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 Joubert syndrome Kallmann syndrome Kawasaki disease Klinefelter syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Mycobacterium avium complex disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Patau syndrome Pick's disease Prader-Willi syndrome Renpenning syndrome Reye syndrome Robinow syndrome Seckel syndrome Sertoli cell-only syndrome Sheehan syndrome Silver-Russell syndrome Sjogren's syndrome Sjogren-Larsson syndrome Smith-Lemli-Opitz syndrome Smith-Magenis syndrome Streptococcus pneumonia T-cell acute lymphoblastic leukemia Usher syndrome type 1 X-linked Aarskog syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 X-linked ichthyosis Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 achondroplasia achromatopsia acoustic neuroma acquired color blindness acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute biphenotypic leukemia acute leukemia acute myeloid leukemia adenocarcinoma in situ adenocarcinoma adenoma adult fibrosarcoma adult liposarcoma adult lymphoma alcoholic hepatitis allergic asthma alopecia amnestic disorder amyloidosis anaplastic astrocytoma androgen insensitivity syndrome androgenic alopecia angioimmunoblastic T-cell lymphoma angiomatous meningioma anhidrosis anogenital venereal wart antithrombin III deficiency aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve insufficiency aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ascending cholangitis asthma ataxia with oculomotor apraxia type 1 atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune thrombocytopenic purpura autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant chondrodysplasia punctata autosomal recessive Robinow syndrome autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis azoospermia bacterial infectious disease bacterial sepsis benign meningioma bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma blastomycosis blue color blindness bone osteosarcoma brain cancer brain infarction breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cataract 9 multiple types cellular schwannoma central nervous system lymphoma cerebral cavernous malformation 1 cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood cerebral astrocytoma childhood liposarcoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholangitis cholera cholesteatoma chondrodysplasia punctata chondrodysplasia-pseudohermaphroditism syndrome chorioamnionitis chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma common wart communication disorder complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital nystagmus congestive heart failure corneal dystrophy coronary artery disease cribriform carcinoma cryptorchidism cutaneous fibrous histiocytoma cystic fibrosis dedifferentiated liposarcoma dermatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma disease of metabolism dissociated nystagmus distal arthrogryposis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epidermodysplasia verruciformis epidermolysis bullosa dystrophica epidermolytic hyperkeratosis epilepsy epithelioid sarcoma esophagus adenocarcinoma essential hypertension essential thrombocythemia essential tremor eunuchism familial mediterranean fever familial nephrotic syndrome fibrillary astrocytoma fibrosarcoma fibrous meningioma gallbladder disease gastroenteritis gastrointestinal system disease gastroparesis gastroschisis gemistocytic astrocytoma generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma hemochromatosis type 1 hemochromatosis hepatic coma hepatic encephalopathy hepatitis C hepatocellular carcinoma hidradenoma high grade glioma human immunodeficiency virus infectious disease hydranencephaly hyperandrogenism hypercalcemia hypertension hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypohidrosis hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism hypopituitarism ichthyosis vulgaris ichthyosis ileitis ileocolitis in situ carcinoma inflammatory bowel disease inherited metabolic disorder intellectual disability intestinal disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma keratoconjunctivitis sicca keratosis follicularis kidney disease kidney failure language disorder large intestine cancer laryngeal squamous cell carcinoma learning disability leprosy lipoid nephrosis liposarcoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphoma malignant astrocytoma malignant peripheral nerve sheath tumor melanoma melanotic neurilemmoma melioidosis meningioma meningothelial meningioma metachromatic leukodystrophy mevalonic aciduria microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma middle cerebral artery infarction migraine mixed glioma mixed oligodendroglioma-astrocytoma mongolian spot mood disorder mucosulfatidosis myelitis myelodysplastic syndrome myelofibrosis nephritis nephrocalcinosis nephronophthisis 1 nephrosis nephrotic syndrome neurilemmoma neurodegenerative disease nodular prostate non-suppurative otitis media non-syndromic X-linked intellectual disability nonpapillary renal cell carcinoma obesity obsolete congenital ichthyosiform erythroderma obsolete ymphosarcoma ocular albinism 1 olfactory groove meningioma oligospermia osteoarthritis osteosarcoma otitis media ovarian cancer ovarian carcinoma palindromic rheumatism pancreatic adenocarcinoma panhypopituitarism papillary renal cell carcinoma papilloma paracoccidioidomycosis parapsoriasis parasagittal meningioma patent ductus arteriosus pathologic nystagmus periodontitis peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma placental choriocarcinoma pleomorphic adenoma pleomorphic liposarcoma plexiform schwannoma pneumocystosis pneumonia polycystic ovary syndrome polyp of middle ear pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postpartum depression primary sclerosing cholangitis prostate cancer prostate carcinoma prostatic adenoma protein C deficiency protein S deficiency protoplasmic astrocytoma psammomatous meningioma pseudohypoparathyroidism pseudoxanthoma elasticum psoriasis pustulosis of palm and sole pyoureter recessive dystrophic epidermolysis bullosa recurrent corneal erosion red color blindness red-green color blindness renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinal disease retinitis retrograde amnesia rheumatoid arthritis rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sclerosing cholangitis seborrheic keratosis secretory meningioma seminoma septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin disease skin melanoma skin papilloma skin tag speech disorder spinal meningioma spindle cell sarcoma spontaneous ocular nystagmus squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma suppurative cholangitis syndromic X-linked intellectual disability Najm type syringoma testicular cancer testicular germ cell cancer testis seminoma thrombophilia tick-borne encephalitis tongue squamous cell carcinoma transitional meningioma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trypanosomiasis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer varicose veins vasculitis visual epilepsy
P39059	Collagen alpha-1(XV) chain	COL15A1	Homo sapiens (human)	27	9
O14657	Torsin-1B	TOR1B DQ1	Homo sapiens (human)	5	9
P24387	Corticotropin-releasing factor-binding protein	CRHBP CRFBP	Homo sapiens (human)	1	9
Q9NR97	Toll-like receptor 8	TLR8	Homo sapiens (human)	23	9
P98172	Ephrin-B1	EFNB1 EFL3 EPLG2 LERK2	Homo sapiens (human)	13	9
Q08174	Protocadherin-1	PCDH1	Homo sapiens (human)	7	9
Q9Y2H9	Microtubule-associated serine/threonine-protein kinase 1	MAST1 KIAA0973 SAST	Homo sapiens (human)	2	9
O15393	Transmembrane protease serine 2	TMPRSS2 PRSS10	Homo sapiens (human)	2	9
Q6PK18	2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3	OGFOD3 C17orf101	Homo sapiens (human)	2	9
Q8TB96	T-cell immunomodulatory protein	ITFG1 LNKN-1 TIP	Homo sapiens (human)	13	9
Q9BU23	Lipase maturation factor 2	LMF2 TMEM112B TMEM153	Homo sapiens (human)	3	9

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