GlyCosmos Portal

Displaying entries **1 - 25** of **16604** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
O75147	Obscurin-like protein 1	KIAA0657 OBSL1	7	1	3-M syndrome
Q14999	Cullin-7	CUL7 KIAA0076	1	1	3-M syndrome
Q96RQ3	Methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial	MCCA MCCC1	2	2	3-methylcrotonyl-CoA carboxylase 1 deficiency
Q9H6K4	Optic atrophy 3 protein	OPA3	1	1	3-methylglutaconic aciduria type 3 optic atrophy 3
P48740	Mannan-binding lectin serine protease 1	CRARF CRARF1 MASP1 PRSS5	6	22	3MC syndrome 1
Q9Y6Z7	Collectin-10	CLL1 COLEC10 UNQ366/PRO702	2	1	3MC syndrome 3
P23945	Follicle-stimulating hormone receptor	FSHR LGR1	4	0	46 XX gonadal dysgenesis ovarian dysgenesis 1 ovarian hyperstimulation syndrome
P24468	COUP transcription factor 2	ARP1 NR2F2 TFCOUP2	1	0	46,XX sex reversal 5
Q8IY37	Probable ATP-dependent RNA helicase DHX37	DDX37 DHX37 KIAA1517	2	1	46,XY complete gonadal dysgenesis
P51843	Nuclear receptor subfamily 0 group B member 1	AHC DAX1 NR0B1	1	1	46,XY sex reversal 2 X-linked adrenal hypoplasia congenita
Q14781	Chromobox protein homolog 2	CBX2	4	1	46,XY sex reversal 5
Q13233	Mitogen-activated protein kinase kinase kinase 1	MAP3K1 MAPKKK1 MEKK MEKK1	7	1	46,XY sex reversal 6 breast cancer diffuse gastric cancer esophagus squamous cell carcinoma lung non-small cell carcinoma rectum cancer stomach cancer
P24530	Endothelin receptor type B	EDNRB ETRB	1	0	ABCD syndrome Hirschsprung's disease Waardenburg syndrome type 4A Waardenburg syndrome asthma
Q5JWF2	Guanine nucleotide-binding protein G(s) subunit alpha isoforms XLas	GNAS GNAS1	2	0	ACTH-independent macronodular adrenal hyperplasia 1 cholangiocarcinoma hypertension obesity pituitary adenoma 3 progressive osseous heteroplasia pseudohypoparathyroidism type 1A pseudohypoparathyroidism type 1B pseudohypoparathyroidism pseudopseudohypoparathyroidism
P40818	Ubiquitin carboxyl-terminal hydrolase 8	KIAA0055 UBPY USP8	3	1	ACTH-secreting pituitary adenoma
P05067	Amyloid-beta precursor protein	A4 AD1 APP	32	19	APP-related cerebral amyloid angiopathy Alzheimer's disease 1 Alzheimer's disease cognitive disorder traumatic brain injury
P46531	Neurogenic locus notch homolog protein 1	NOTCH1 TAN1	58	12	Adams-Oliver syndrome adult T-cell leukemia/lymphoma aortic valve disease 1 congenital heart disease
Q2M1Z3	Rho GTPase-activating protein 31	ARHGAP31 CDGAP KIAA1204	2	1	Adams-Oliver syndrome coronary artery disease
Q06330	Recombining binding protein suppressor of hairless	IGKJRB IGKJRB1 RBPJ RBPJK RBPSUH	2	1	Adams-Oliver syndrome dilated cardiomyopathy
Q9NR61	Delta-like protein 4	DLL4 UNQ1895/PRO4341	4	0	Adams-Oliver syndrome limb ischemia
Q96HP0	Dedicator of cytokinesis protein 6	DOCK6 KIAA1395	4	2	Adams-Oliver syndrome
Q5NDL2	EGF domain-specific O-linked N-acetylglucosamine transferase	AER61 C3orf64 EOGT EOGT1	3	6	Adams-Oliver syndrome
P01911	HLA class II histocompatibility antigen, DRB1 beta chain	HLA-DRB1	1	56	Addison's disease Alport syndrome Alzheimer's disease Behcet's disease Chagas disease Graves' disease Hantavirus hemorrhagic fever with renal syndrome Human papillomavirus infectious disease Meniere's disease Parkinson's disease Sjogren's syndrome Takayasu's arteritis Vogt-Koyanagi-Harada disease abdominal aortic aneurysm acute disseminated encephalomyelitis allergic asthma allergic bronchopulmonary aspergillosis allergic disease alveolar echinococcosis ankylosing spondylitis anti-basement membrane glomerulonephritis antiphospholipid syndrome aspirin-induced respiratory disease asthma atrophic gastritis autistic disorder autoimmune disease autoimmune hepatitis autoimmune polyendocrine syndrome type 2 autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis bacterial infectious disease breast cancer breast carcinoma celiac disease cerebral infarction cervix uteri carcinoma in situ choreatic disease cicatricial pemphigoid cystic echinococcosis diabetic angiopathy diabetic retinopathy endometriosis glaucoma hepatitis C human immunodeficiency virus infectious disease hypothyroidism idiopathic pulmonary fibrosis infectious mononucleosis juvenile rheumatoid arthritis latex allergy leprosy liver cirrhosis lupus nephritis mixed connective tissue disease multidrug-resistant tuberculosis multiple sclerosis myasthenia gravis myositis narcolepsy neuromyelitis optica optic neuritis paracoccidioidomycosis pemphigus peptic ulcer disease polyneuropathy primary progressive multiple sclerosis prostate cancer pulmonary sarcoidosis pulmonary tuberculosis pure red-cell aplasia renal cell carcinoma retinopathy of prematurity rheumatic fever rheumatic heart disease rheumatoid arthritis sarcoidosis schistosomiasis sensorineural hearing loss severe acute respiratory syndrome sympathetic ophthalmia systemic lupus erythematosus temporal arteritis thromboangiitis obliterans tuberculosis type 1 diabetes mellitus typhoid fever urticaria uveitis uveoparotid fever vitiligo vulva cancer
P01920	HLA class II histocompatibility antigen, DQ beta 1 chain	HLA-DQB HLA-DQB1	2	0	Addison's disease Behcet's disease Creutzfeldt-Jakob disease Crohn's disease Graves' disease HTLV-1-associated myelopathy/tropical spastic paraparesis IgA glomerulonephritis Plasmodium falciparum malaria Sjogren's syndrome Stevens-Johnson syndrome Vogt-Koyanagi-Harada disease achalasia acute disseminated encephalomyelitis acute lymphoblastic leukemia acute myeloid leukemia agranulocytosis allergic bronchopulmonary aspergillosis allergic disease alopecia areata alveolar echinococcosis ankylosing spondylitis antiphospholipid syndrome aplastic anemia arthritis aspirin-induced respiratory disease asthma atrophic gastritis autoimmune disease autoimmune hepatitis autoimmune pancreatitis autoimmune polyendocrine syndrome type 2 autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis bacterial infectious disease beta thalassemia celiac disease cervical cancer cervical dystonia chikungunya choreatic disease chronic myeloid leukemia cicatricial pemphigoid colorectal cancer common variable immunodeficiency common wart cystic echinococcosis degenerative myopia dental caries diabetic retinopathy dilated cardiomyopathy 1H dilated cardiomyopathy erythema multiforme glaucoma hepatitis B hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease hyperthyroidism hypothyroidism immunoglobulin alpha deficiency iridocyclitis juvenile rheumatoid arthritis latex allergy liver cirrhosis marginal zone lymphoma multidrug-resistant tuberculosis multiple sclerosis myasthenia gravis mycosis fungoides myocarditis myositis narcolepsy neuromyelitis optica optic neuritis osteomyelitis paroxysmal nocturnal hemoglobinuria pemphigus vulgaris pemphigus pneumoconiosis pre-eclampsia primary progressive multiple sclerosis primary sclerosing cholangitis psoriasis pulmonary tuberculosis pure red-cell aplasia rheumatic fever rheumatic heart disease rheumatoid arthritis rhinitis rhinoscleroma sarcoidosis sickle cell anemia silicosis stomach disease systemic lupus erythematosus thrombotic thrombocytopenic purpura tuberculosis type 1 diabetes mellitus typhoid fever ulcerative colitis vitiligo vulva cancer
P33076	MHC class II transactivator	CIITA MHC2TA	5	1	Addison's disease MHC class II deficiency juvenile rheumatoid arthritis multiple sclerosis myocardial infarction rheumatoid arthritis systemic lupus erythematosus

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