GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
O75151	Lysine-specific demethylase PHF2	PHF2 CENP-35 KIAA0662	1	2
P51452	Dual specificity protein phosphatase 3	DUSP3 VHR	1	2
Q9BY07	Electrogenic sodium bicarbonate cotransporter 4	SLC4A5 NBC4	1	2
O43719	17S U2 SnRNP complex component HTATSF1	HTATSF1	1	2
Q96C57	Protein CUSTOS	CUSTOS C12orf43	2	2
Q6H9L7	Isthmin-2	ISM2 TAIL1 THSD3	8	2
Q07021	Complement component 1 Q subcomponent-binding protein, mitochondrial	C1QBP GC1QBP HABP1 SF2P32	2	2
Q9BXN2	C-type lectin domain family 7 member A	CLEC7A BGR CLECSF12 DECTIN1	3	2	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 Behcet's disease Bloch-Sulzberger syndrome Kawasaki disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Pick's disease Reye syndrome acquired hyperkeratosis acute myeloid leukemia adult-onset Still's disease allergic asthma amyloidosis angular cheilitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aspergillosis asthma atherosclerosis atopic dermatitis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome bacterial infectious disease bacterial sepsis black piedra blastomycosis cancer candidiasis cerebral degeneration cheilitis cholesteatoma chromoblastomycosis chronic mucocutaneous candidiasis chronic obstructive pulmonary disease chronic ulcer of skin coccidioidomycosis colitis congenital intrinsic factor deficiency coronary artery disease cryptococcosis cutaneous leishmaniasis cystic fibrosis dermatitis dermatomycosis dermatophytosis diverticulitis embryoma epilepsy exanthem fungal infectious disease gastroenteritis granuloma annulare hepatitis B hepatitis hepatocellular carcinoma histoplasmosis hypomelanosis of Ito ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intrinsic asthma keratitis keratoconjunctivitis lip disease liver cancer liver carcinoma liver cirrhosis lupus nephritis male infertility mycotic corneal ulcer nutmeg liver obesity oral candidiasis osteoarthritis pancreatic cancer pancreatic carcinoma paracoccidioidomycosis parapsoriasis parasitic helminthiasis infectious disease patent ductus arteriosus pneumocystosis pneumonia polyp of middle ear psoriasis pustulosis of palm and sole rheumatoid arthritis shigellosis sporotrichosis superficial mycosis systemic lupus erythematosus tinea favosa tuberculosis ulcerative colitis urinary tract obstruction vasculitis visual epilepsy vulvovaginal candidiasis white piedra
Q8N6Y1	Protocadherin-20	PCDH20 PCDH13	8	2
Q04656	Copper-transporting ATPase 1	ATP7A MC1 MNK	3	2
Q9P2N2	Rho GTPase-activating protein 28	ARHGAP28 KIAA1314	1	2
Q9NX40	OCIA domain-containing protein 1	OCIAD1 ASRIJ OCIA	2	2
O75083	WD repeat-containing protein 1	WDR1	1	2
Q96ST2	Protein IWS1 homolog	IWS1 IWS1L	7	2
P05023	Sodium/potassium-transporting ATPase subunit alpha-1	ATP1A1	2	2
Q13018	Secretory phospholipase A2 receptor	PLA2R1 CLEC13C	3	2	IgA glomerulonephritis T-cell acute lymphoblastic leukemia Werner syndrome acute biphenotypic leukemia acute leukemia acute myeloid leukemia adrenoleukodystrophy allergic asthma asthma autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer cardiac arrest childhood leukemia chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma collecting duct carcinoma embryoma essential thrombocythemia familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease interstitial nephritis intrinsic asthma kidney cancer kidney disease leukemia lipoid nephrosis lupus erythematosus lupus nephritis membranous glomerulonephritis myelodysplastic syndrome nephritis nephrosis nephrotic syndrome nonpapillary renal cell carcinoma papillary renal cell carcinoma progeria prostate cancer prostate carcinoma pyelitis pyelonephritis pyoureter renal carcinoma renal cell carcinoma renal infectious disease sarcomatoid renal cell carcinoma substance abuse substance-related disorder systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma
Q96RQ3	Methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial	MCCC1 MCCA	2	2
Q9UQ13	Leucine-rich repeat protein SHOC-2	SHOC2 KIAA0862	1	2
Q9UPT6	C-Jun-amino-terminal kinase-interacting protein 3	MAPK8IP3 JIP3 KIAA1066	1	2
Q9UIA9	Exportin-7	XPO7 KIAA0745 RANBP16	1	2
Q8NBU5	Outer mitochondrial transmembrane helix translocase	ATAD1	1	2
Q13613	Myotubularin-related protein 1	MTMR1	2	2	Charcot-Marie-Tooth disease type 4B1 centronuclear myopathy X-linked centronuclear myopathy congenital structural myopathy myotonic dystrophy type 1 myotonic dystrophy type 2
P57071	PR domain zinc finger protein 15	PRDM15 C21orf83 ZNF298	1	2
Q8N967	Leucine-rich repeat and transmembrane domain-containing protein 2	LRTM2	5	2
Q15125	3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase	EBP	3	2	Alzheimer's disease Balo concentric sclerosis Dandy-Walker syndrome Klinefelter syndrome Klippel-Feil syndrome Krabbe disease Laron syndrome Marfan syndrome Patau syndrome Peters anomaly Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 X-linked cleft palate with or without ankyloglossia achondroplasia actinic keratosis acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute promyelocytic leukemia adrenoleukodystrophy adult fibrosarcoma allergic asthma alopecia ankyloglossia aortic valve disease 2 aortic valve stenosis arteriosclerotic cardiovascular disease asthma atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis bladder carcinoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cartilage-hair hypoplasia cataract central nervous system cancer central nervous system disease cerebral artery occlusion cerebral infarction cerebrovascular disease childhood acute myeloid leukemia childhood leukemia chondrodysplasia punctata choriocarcinoma chromophobe renal cell carcinoma chronic monocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma cleft palate clubfoot collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congenital heart disease congenital nystagmus congenital ptosis congestive heart failure cornea plana coronary artery disease cryptorchidism cystic fibrosis dementia diabetes mellitus dissociated nystagmus embryoma epilepsy essential hypertension essential thrombocythemia familial retinoblastoma fibrosarcoma gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gliosarcoma granuloma annulare hematologic cancer hemophilia B hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hydrocephalus hydronephrosis hyperostosis hypertension ichthyosis intellectual disability intrinsic asthma isolated cleft palate keratosis follicularis kidney failure large intestine cancer laryngeal disease learning disability leiomyoma leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 melanoma microphthalmia mixed glioma mixed-type liposarcoma mongolian spot mucopolysaccharidosis IV multicentric Castleman disease multiple epiphyseal dysplasia myelodysplastic syndrome myeloid leukemia myofibroma myxoid liposarcoma narcolepsy nervous system disease neuroblastoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete congenital ichthyosiform erythroderma obstructive hydrocephalus optic atrophy osteochondrodysplasia osteomyelitis papillary adenocarcinoma papillary renal cell carcinoma papilloma pathologic nystagmus placenta cancer polydactyly polyhydramnios pseudoxanthoma elasticum ptosis renal carcinoma renal cell carcinoma retinoblastoma rheumatoid arthritis rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 sarcomatoid renal cell carcinoma schizophrenia scoliosis seborrheic keratosis senile degeneration of brain sensorineural hearing loss situs inversus skin disease skin melanoma spondylolisthesis spontaneous ocular nystagmus squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal calcification tracheal disease tracheal stenosis trilateral retinoblastoma tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer uterine fibroid visual epilepsy

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