GlyCosmos Portal

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UniProt ID	Protein Name ▼	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9BRV8	Suppressor of IKBKE 1	SIKE1 SIKE	0	1
Q5SSQ6	Suppressor APC domain-containing protein 1	SAPCD1 C6orf26 G7D NG23	1	1
O95425	Supervillin	SVIL	3	1
P04179	Superoxide dismutase [Mn], mitochondrial	SOD2	2	3
P00441	Superoxide dismutase [Cu-Zn]	SOD1	1	3
Q9GZS3	Superkiller complex protein 8	SKIC8 WDR61	0	1
Q6PGP7	Superkiller complex protein 3	SKIC3 KIAA0372 TTC37	0	1
Q15477	Superkiller complex protein 2	SKIC2 DDX13 SKI2W SKIV2 SKIV2L W	0	1
Q9BR01	Sulfotransferase 4A1	SULT4A1 SULTX3	0	1
Q6IMI6	Sulfotransferase 1C3	SULT1C3	0	1
O00338	Sulfotransferase 1C2	SULT1C2 SULT1C1	2	1
O43704	Sulfotransferase 1B1	SULT1B1 ST1B2 SULT1B2	1	1
P0DMN0	Sulfotransferase 1A4	SULT1A4	0	1
P0DMM9	Sulfotransferase 1A3	SULT1A3 STM	0	1
P50226	Sulfotransferase 1A2	SULT1A2 STP2	0	1
P50225	Sulfotransferase 1A1	SULT1A1 STP STP1	0	1
Q9Y6N5	Sulfide:quinone oxidoreductase, mitochondrial	SQOR SQRDL	1	2
Q6ZRP7	Sulfhydryl oxidase 2	QSOX2 QSCN6L1 SOXN	20	7
O00391	Sulfhydryl oxidase 1	QSOX1 QSCN6	28	38
H0Y430	Sulfhydryl oxidase (Fragment)	QSOX2	1	0
A0A140VKE5	Sulfhydryl oxidase	QSCN6	1	0
P50443	Sulfate transporter	SLC26A2 DTD DTDST	3	0	Baraitser-Winter syndrome Bartter disease Clostridium difficile colitis Conn's syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Pendred Syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome achondrogenesis type IB achondroplasia adenocarcinoma adenoma arthritis arthropathy atelosteogenesis auditory system disease autosomal recessive osteopetrosis 7 benign mesothelioma branchiootic syndrome breast cancer cancer chondrodysplasia punctata cleft palate clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure cryptorchidism cystic lymphangioma diarrhea diastrophic dysplasia disease of metabolism dyshormonogenic goiter embryoma endometritis fibrosarcoma follicular adenoma inguinal hernia irritable bowel syndrome isolated cleft palate juvenile rheumatoid arthritis large intestine cancer laryngostenosis lingual-facial-buccal dyskinesia lung benign neoplasm lung cancer lung non-small cell carcinoma malignant mesothelioma mastitis microcystic adenoma movement disease mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia 4 multiple epiphyseal dysplasia neurocirculatory asthenia omphalocele orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis osteochondrodysplasia osteopetrosis osteoporosis osteosclerosis otosclerosis papillary adenoma placental insufficiency polyhydramnios primary hyperaldosteronism scoliosis sensorineural hearing loss spinal cord disease spondylolysis stomach cancer stomach carcinoma umbilical hernia
Q9H2B4	Sulfate anion transporter 1	SLC26A1 SAT1	2	0
B1AMP9	Sulfatase 2 (Fragment)	SULF2	1	0
Q8NCC5	Sugar phosphate exchanger 3	SLC37A3 SPX3	2	0

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