GlyCosmos Portal

Displaying entries **18126 - 18150** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
O94856	Neurofascin	NFASC KIAA0756	15	34
Q9BX97	Plasmalemma vesicle-associated protein	PLVAP FELS PV1	5	34
O60487	Myelin protein zero-like protein 2	MPZL2 EVA EVA1	4	34
Q12797	Aspartyl/asparaginyl beta-hydroxylase	ASPH BAH	12	34
P09758	Tumor-associated calcium signal transducer 2	TACSTD2 GA733-1 M1S1 TROP2	7	34
Q11201	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1	ST3GAL1 SIAT4 SIAT4A	6	34	Graves' disease bipolar disorder bladder carcinoma breast cancer breast carcinoma cancer cervical squamous cell carcinoma chronic myeloid leukemia embryoma hyperthyroidism mucopolysaccharidosis IV mucopolysaccharidosis IVA ovarian cancer ovarian carcinoma ovary serous adenocarcinoma prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder scleroderma skin squamous cell carcinoma systemic scleroderma thyrotoxicosis urinary bladder cancer
O15455	Toll-like receptor 3	TLR3	17	34
Q8NFZ8	Cell adhesion molecule 4	CADM4 IGSF4C NECL4 TSLL2	6	34
P00742	Coagulation factor X	F10	13	35
Q02985	Complement factor H-related protein 3	CFHR3 CFHL3 FHR3	4	35
P22792	Carboxypeptidase N subunit 2	CPN2 ACBP	8	35
O95302	Peptidyl-prolyl cis-trans isomerase FKBP9	FKBP9 FKBP60 FKBP63	4	36
Q9NV96	Cell cycle control protein 50A	TMEM30A C6orf67 CDC50A	8	36
P10643	Complement component C7	C7	9	36
Q04900	Sialomucin core protein 24	CD164	16	36
P56817	Beta-secretase 1	BACE1 BACE KIAA1149	5	36
Q13361	Microfibrillar-associated protein 5	MFAP5 MAGP2	3	36
Q9NUN5	Lysosomal cobalamin transport escort protein LMBD1	LMBRD1 C6orf209 NESI	7	36
Q969P0	Immunoglobulin superfamily member 8	IGSF8 CD81P3 EWI2 KCT4	4	36
P14384	Carboxypeptidase M	CPM	7	36	adult liposarcoma anthracosilicosis anxiety disorder aphasia asbestosis atrial fibrillation breast cancer breast carcinoma cancer childhood liposarcoma colorectal cancer colorectal carcinoma embryoma endometriosis of ovary endometriosis generalized anxiety disorder inflammatory liposarcoma kidney failure large intestine cancer lipoma liposarcoma lung adenocarcinoma lung cancer multiple symmetric lipomatosis pleomorphic lipoma pleomorphic liposarcoma proliferative diabetic retinopathy sclerosing liposarcoma silicosis well-differentiated liposarcoma
Q07837	Amino acid transporter heavy chain SLC3A1	SLC3A1 NBAT	6	37	IgA glomerulonephritis Marfan syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction 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 breast cancer breast carcinoma bulimia nervosa calcinosis calcium metabolism disease cancer chronic kidney disease colon carcinoma colorectal cancer congenital myasthenic syndrome 22 congenital ptosis coronary thrombosis cystinuria diabetes mellitus diabetic ketoacidosis distal myopathy epilepsy essential hypertension facioscapulohumeral muscular dystrophy galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease high grade glioma hypercalcemia hypertension hypoglycemia hypogonadism hypotonia-cystinuria syndrome interstitial nephritis kidney failure lactic acidosis limb-girdle muscular dystrophy muscular dystrophy myocardial infarction nephrocalcinosis nephrolithiasis nephrosclerosis 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 panic disorder phosphorus metabolism disease primary pulmonary hypertension prostate cancer prostate carcinoma ptosis pyelitis pyelonephritis renal hypertension renal infectious disease silent myocardial infarction situs inversus synovial sarcoma tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis urinary tract obstruction vesicoureteral reflux visual epilepsy
Q8IV08	5'-3' exonuclease PLD3	PLD3	6	37	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 Henoch-Schoenlein purpura Pick's disease Reye syndrome amyloidosis atopic dermatitis cerebral degeneration congenital nystagmus conjunctival folliculosis conjunctivitis dermatitis dissociated nystagmus hypersensitivity vasculitis keratitis keratoconjunctivitis pathologic nystagmus rheumatoid arthritis scleroderma shipyard eye spinocerebellar ataxia 46 spontaneous ocular nystagmus systemic scleroderma
Q86SQ4	Adhesion G-protein coupled receptor G6	ADGRG6 DREG GPR126 VIGR	26	37
Q9Y639	Neuroplastin	NPTN SDFR1 SDR1	8	37
Q6UWY5	Olfactomedin-like protein 1	OLFML1	3	37

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