GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
O95858	Tetraspanin-15	TSPAN15 NET7 TM4SF15	3	3
A0A7I2V3B5	ADAM metallopeptidase domain 9	ADAM9	3	0
Q4ZG55	Protein GREB1	GREB1 KIAA0575	3	1
Q5U651	Ras-interacting protein 1	RASIP1	3	1
P14317	Hematopoietic lineage cell-specific protein	HCLS1 HS1	3	2
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
Q8IX01	SURP and G-patch domain-containing protein 2	SUGP2 KIAA0365 SFRS14	3	1
P05111	Inhibin alpha chain	INHA	3	0
Q92643	GPI-anchor transamidase	PIGK GPI8	3	1	adult lymphoma cancer central nervous system lymphoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer lymphoma obsolete ymphosarcoma
Q5H9R7	Serine/threonine-protein phosphatase 6 regulatory subunit 3	PPP6R3 C11orf23 KIAA1558 PP6R3 SAPL SAPS3	3	18
Q9UN66	Protocadherin beta-8	PCDHB8 PCDH3I	3	1
Q8N365	Circadian-associated transcriptional repressor	CIART C1orf51	3	1
Q17R55	Protein FAM187B	FAM187B TMEM162	3	0
Q6ZSZ6	Teashirt homolog 1	TSHZ1 SDCCAG33 TSH1	3	2
O95782	AP-2 complex subunit alpha-1	AP2A1 ADTAA CLAPA1	3	2
Q96M86	Dynein heavy chain domain-containing protein 1	DNHD1 C11orf47 CCDC35 DHCD1 DNHD1L	3	1
Q9UE03	MICA protein (Fragment)	MICA	3	0
P07998	Ribonuclease pancreatic	RNASE1 RIB1 RNS1	3	3
E5RJG5	Solute carrier family 39 member 14 (Fragment)	SLC39A14	3	0
P34820	Bone morphogenetic protein 8B	BMP8B BMP8	3	2
Q14916	Sodium-dependent phosphate transport protein 1	SLC17A1 NPT1	3	0
Q8N109	Killer cell immunoglobulin-like receptor 2DL5A	KIR2DL5A CD158F CD158F1 KIR2DL5	3	0
Q9NS64	Protein reprimo	RPRM	3	1
A0A0K0Q2Z1	Antithrombin-III	SERPINC1	3	0
A0A7I2V3W3	ADAM metallopeptidase domain 9	ADAM9	3	0

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