GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
B3KNK9	Epididymis luminal protein 46	GOLPH2 HEL46	2	0
Q6P4E1	Protein GOLM2	GOLM2 CASC4	23	9
C9JYM4	Golgi membrane protein 1 (Fragment)	GOLM1	1	0
Q8NBJ4	Golgi membrane protein 1	GOLM1 C9orf155 GOLPH2	18	61
O00461	Golgi integral membrane protein 4	GOLIM4 GIMPC GOLPH4 GPP130	27	8
Q14789	Golgin subfamily B member 1	GOLGB1	1	1
A8MQT2	Golgin subfamily A member 8B	GOLGA8B	1	3
A7E2F4	Golgin subfamily A member 8A	GOLGA8A KIAA0855	1	3
A8MZA4	Golgin subfamily A member 6-like protein 6	GOLGA6L6	1	1
H0YM25	Golgin subfamily A member 6-like protein 22	GOLGA6L22	1	1
Q8N9W4	Golgin subfamily A member 6-like protein 2	GOLGA6L2	1	1
Q8N7Z2	Golgin subfamily A member 6-like protein 1	GOLGA6L1	1	1
Q13439	Golgin subfamily A member 4	GOLGA4	2	11
Q08378	Golgin subfamily A member 3	GOLGA3	4	1
Q08379	Golgin subfamily A member 2	GOLGA2	1	1
H7C3P4	N-acetylglucosamine-6-sulfatase	GNS	5	0
F5H4C6	Glucosamine (N-acetyl)-6-sulfatase (Fragment)	GNS	5	0
A0A024RBC5	Glucosamine (N-acetyl)-6-sulfatase (Sanfilippo disease IIID), isoform CRA_a (Fragment)	GNS	5	0
P15586	N-acetylglucosamine-6-sulfatase	GNS	21	118	brain cancer cancer diarrhea epilepsy fundus dystrophy hypertrichosis hypertrophic cardiomyopathy 1 intellectual disability learning disability low tension glaucoma lysosomal storage disease melanoma 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 rheumatoid arthritis sensorineural hearing loss skin melanoma visual epilepsy
H0YFA9	Glucosamine (N-acetyl)-6-sulfatase (Fragment)	GNS	2	0
F6S8M0	Glucosamine (N-acetyl)-6-sulfatase	GNS	5	0
P30968	Gonadotropin-releasing hormone receptor	GNRHR GRHR	2	0
Q9UJJ9	N-acetylglucosamine-1-phosphotransferase subunit gamma	GNPTG C16orf27 GNPTAG	11	20	Fabry disease Laron syndrome achondroplasia alexia aortic valve disease 2 aortic valve insufficiency aortic valve stenosis chylomicron retention disease cone-rod dystrophy dyslexia fundus albipunctatus glycoproteinosis lipid storage disease lysosomal storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myopia osteochondrodysplasia retinitis pigmentosa scoliosis stuttering
Q3T906	N-acetylglucosamine-1-phosphotransferase subunits alpha/beta	GNPTAB GNPTA KIAA1208	42	24	Ebola hemorrhagic fever Fabry disease Laron syndrome Legg-Calve-Perthes disease Scheuermann's disease achondroplasia alexia anemia aortic valve insufficiency arrhythmogenic right ventricular cardiomyopathy autistic disorder cancer capillary hemangioma cardiomyopathy cavernous hemangioma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma clubfoot collecting duct carcinoma congenital central hypoventilation syndrome congestive heart failure corneal dystrophy craniosynostosis disease of metabolism dyslexia embryoma endomyocardial fibrosis enterocele familial hypertrophic cardiomyopathy glycoproteinosis hemangioma hypertrophic cardiomyopathy inguinal hernia intellectual disability keratosis follicularis learning disability lipid storage disease lysosomal storage disease macrocytic anemia megalocornea mixed sleep apnea mongolian spot mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia nonpapillary renal cell carcinoma obstructive sleep apnea omphalocele osteochondrodysplasia papillary renal cell carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinal degeneration retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis sleep apnea spinal cord disease stuttering syringomyelia umbilical hernia
Q96EK6	Glucosamine 6-phosphate N-acetyltransferase	GNPNAT1 GNA1	0	1	diabetes mellitus diabetic ketoacidosis type 2 diabetes mellitus

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