GlyCosmos Portal

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UniProt ID	Protein Name ▼	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
R4GMX5	Basigin (Fragment)	BSG	1	0
Q54A51	Basigin	hEMMPRIN BSG	3	0
A0A087WUV8	Basigin	BSG	2	0
A0A7P0TA85	Basigin	BSG	3	0
P35613	Basigin	BSG	12	63
A0A7P0T8A7	Basigin	BSG	2	0
A0A7P0TB04	Basigin	BSG	3	0
P10163	Basic salivary proline-rich protein 4	PRB4	8	0
Q04118	Basic salivary proline-rich protein 3	PRB3	10	0
P02812	Basic salivary proline-rich protein 2	PRB2	4	0
P04280	Basic salivary proline-rich protein 1	PRB1	4	0
Q8N1L9	Basic leucine zipper transcriptional factor ATF-like 2	BATF2	0	1
Q16520	Basic leucine zipper transcriptional factor ATF-like	BATF	0	1
Q68DE3	Basic helix-loop-helix domain-containing protein USF3	USF3 KIAA2018	5	1
O00327	Basic helix-loop-helix ARNT-like protein 1	BMAL1 ARNTL BHLHE5 MOP3 PASD3	1	1
P98160	Basement membrane-specific heparan sulfate proteoglycan core protein	HSPG2	85	182	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 Balkan nephropathy Bethlem myopathy Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 HELLP syndrome IgA glomerulonephritis Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome 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 Norum disease Ollier disease Peters anomaly Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Schwartz-Jampel syndrome 1 Seckel syndrome Silver-Russell syndrome Silverman-Handmaker type dyssegmental dysplasia Stevens-Johnson syndrome Tangier disease Werdnig-Hoffmann disease X-linked Aarskog syndrome X-linked spondyloepiphyseal dysplasia tarda abdominal obesity-metabolic syndrome 1 abetalipoproteinemia achondroplasia acute promyelocytic leukemia adenoid cystic carcinoma adenoma adrenoleukodystrophy adult fibrosarcoma adult oligodendroglioma age related macular degeneration alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis ameloblastoma amyloidosis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 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 Robinow syndrome 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 autosomal recessive osteopetrosis 7 benign mastocytoma bipolar disorder blepharophimosis blepharospasm blindness brain stem infarction breast cancer bronchus cancer bronchus carcinoma cancer carcinoma cataract central nervous system cancer cerebral amyloid angiopathy cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood oligodendroglioma childhood spinal muscular atrophy cholangiocarcinoma chondrocalcinosis chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma choreaacanthocytosis chronic lymphocytic leukemia chronic myeloid leukemia cleft palate cleidocranial dysplasia clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cornea plana coronary artery disease cystic fibrosis degeneration of macula and posterior pole dextro-looped transposition of the great arteries diabetes mellitus diabetic ketoacidosis disease of mental health distal myopathy embryoma enthesopathy epidermolysis bullosa epilepsy erythema multiforme esophageal cancer esophageal carcinoma exostosis extracutaneous mastocytoma facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hypercholesterolemia familial hyperlipidemia familial nephrotic syndrome fibromyalgia fibrosarcoma focal hand dystonia follicular adenoma fragile X syndrome gallbladder cancer gallbladder carcinoma gas gangrene generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatitis B hepatitis C hepatitis E hepatoblastoma hepatocellular carcinoma hereditary multiple exostoses high grade glioma humeroradial synostosis hydranencephaly hypereosinophilic syndrome hyperglycemia hypolipoproteinemia immune system disease in situ carcinoma interstitial nephritis intracranial aneurysm intrahepatic cholangiocarcinoma isolated cleft palate isolated ectopia lentis isolated elevated serum creatine phosphokinase levels juvenile spinal muscular atrophy kidney disease kidney failure large intestine cancer leech infestation limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lipoid nephrosis lissencephaly liver cancer liver carcinoma liver cirrhosis low compliance bladder lung cancer lung carcinoma lupus erythematosus lupus nephritis macular degeneration malignant epithelial mesothelioma malignant hyperthermia mast cell neoplasm mastocytosis melanoma membranous glomerulonephritis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly microcystic adenoma mixed glioma mixed oligodendroglioma-astrocytoma mucopolysaccharidosis IV multiple epiphyseal dysplasia multiple types of congenital heart defects 6 muscular dystrophy musculoskeletal system disease myiasis myopia myositis myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nephritis nephrolithiasis nephrosis nephrotic syndrome type 1 nephrotic syndrome nutmeg liver obesity 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 obsolete dextro-looped transposition of the great arteries 1 obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy oligodendroglioma osteoarthritis osteochondrodysplasia osteopetrosis osteoporosis osteosclerosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary carcinoma periarthritis polyhydramnios pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pre-eclampsia primary pulmonary hypertension progressive muscular atrophy prostate cancer prostate carcinoma proximal symphalangism pseudosarcomatous fibromatosis psychotic disorder pyelitis pyelonephritis pyoureter radioulnar synostosis renal infectious disease salivary gland adenoid cystic carcinoma sarcomatoid carcinoma schizophrenia scleroderma scoliosis short-rib thoracic dysplasia 14 with polydactyly sick sinus syndrome skin melanoma spermatic cord torsion spinal muscular atrophy squamous cell carcinoma steatotic liver disease syndromic X-linked intellectual disability Najm type systemic lupus erythematosus systemic scleroderma tendinitis thanatophoric dysplasia thrombocytopenia thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma toxic shock syndrome toxoplasmosis tuberculosis 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 uremia uric acid nephrolithiasis urticaria pigmentosa uveal melanoma
A0A172M5V3	Basal cell adhesion molecule Lutheran blood group (Fragment)	BCAM	2	0
A0A068W6H0	Basal cell adhesion molecule (Lutheran blood group)	BCAM	3	0
A0A087WXM8	Basal cell adhesion molecule (Lutheran blood group)	BCAM	3	0
A0A1Z1VXG5	Basal cell adhesion molecule (Fragment)	BCAM	3	0
P50895	Basal cell adhesion molecule	BCAM LU MSK19	7	66
Q8ND07	Basal body-orientation factor 1	BBOF1 C14orf45 CCDC176	0	1
O75531	Barrier-to-autointegration factor	BANF1 BAF BCRG1	0	1
Q9BXC9	Bardet-Biedl syndrome 2 protein	BBS2	1	1
Q9BZE3	BarH-like 1 homeobox protein	BARHL1	1	1

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