GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P37173	TGF-beta receptor type-2	TGFBR2	7	12
P51688	N-sulphoglucosamine sulphohydrolase	SGSH HSS	6	12	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 Balo concentric sclerosis Kearns-Sayre syndrome Kluver-Bucy syndrome Pick's disease Reye syndrome Schwartz-Jampel syndrome 1 Stevens-Johnson syndrome adrenoleukodystrophy ankylosing spondylitis anorexia nervosa arthritis arthropathy beta-mannosidosis cancer cardiomyopathy central nervous system disease central nervous system origin vertigo cerebral degeneration chronic obstructive pulmonary disease cone-rod dystrophy congenital nystagmus depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dissociated nystagmus embryoma endomyocardial fibrosis eosinophilic esophagitis epilepsy fundus albipunctatus fundus dystrophy hypertrichosis hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease major depressive disorder melancholic depression movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis mucosulfatidosis multiple epiphyseal dysplasia narcolepsy nervous system disease neurodegeneration with brain iron accumulation neurodegenerative disease obsolete melancholia osteoarthritis osteochondrodysplasia pathologic nystagmus retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus visual epilepsy
Q969V3	BOS complex subunit NCLN	NCLN	4	12
Q6UXG2	Endosome/lysosome-associated apoptosis and autophagy regulator 1	ELAPOR1 EIG121 KIAA1324	8	12
Q6NSJ0	Myogenesis-regulating glycosidase	MYORG KIAA1161	6	12	amnestic disorder basal ganglia calcification choreatic disease dystonia epilepsy hydrocephalus lingual-facial-buccal dyskinesia microcephaly migraine neurodegenerative disease placental insufficiency recurrent corneal erosion retrograde amnesia secondary Parkinson disease syndromic X-linked intellectual disability type 10 thrombocytopenia visual epilepsy
Q53RD9	Fibulin-7	FBLN7 TM14	6	12
Q9H173	Nucleotide exchange factor SIL1	SIL1	16	12
Q9Y2J2	Band 4.1-like protein 3	EPB41L3 DAL1 KIAA0987	3	12
Q15155	BOS complex subunit NOMO1	NOMO1 PM5	6	12
Q16787	Laminin subunit alpha-3	LAMA3 LAMNA	18	12
P58166	Inhibin beta E chain	INHBE	4	12
Q8WTV0	Scavenger receptor class B member 1	SCARB1 CD36L1 CLA1	13	12
P10451	Osteopontin	SPP1 BNSP OPN	11	12
Q8NBK3	Formylglycine-generating enzyme	SUMF1	2	12	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
P01133	Pro-epidermal growth factor	EGF	15	12
P10153	Non-secretory ribonuclease	RNASE2 EDN RNS2	6	12
Q16769	Glutaminyl-peptide cyclotransferase	QPCT	5	12
P07858	Cathepsin B	CTSB CPSB	3	12
Q9H792	Inactive tyrosine-protein kinase PEAK1	PEAK1 KIAA2002	7	12
P09668	Pro-cathepsin H	CTSH CPSB	6	12
Q92563	Testican-2	SPOCK2 KIAA0275 TICN2	7	12
P09172	Dopamine beta-hydroxylase	DBH	4	12
Q6V0I7	Protocadherin Fat 4	FAT4 CDHF14 FATJ	43	12
Q02763	Angiopoietin-1 receptor	TEK TIE2 VMCM VMCM1	10	12
Q99784	Noelin	OLFM1 NOE1 NOEL1	8	13

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