GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q15555	Microtubule-associated protein RP/EB family member 2	MAPRE2 RP1	1	1
Q53H76	Phospholipase A1 member A	PLA1A NMD PSPLA1	2	1
Q53EZ4	Centrosomal protein of 55 kDa	CEP55 C10orf3 URCC6	0	1
Q96JP2	Unconventional myosin-XVB	MYO15B KIAA1783 MYO15BP	1	1
P28065	Proteasome subunit beta type-9	PSMB9 LMP2 PSMB6i RING12	0	1
Q9H3K6	BolA-like protein 2	BOLA2 BOLA2B BOLA2A	0	1
Q9NWS0	PIH1 domain-containing protein 1	PIH1D1 NOP17	0	1
P13489	Ribonuclease inhibitor	RNH1 PRI RNH	0	1
Q86SU0	Immunoglobulin-like domain-containing receptor 1	ILDR1	2	1
Q9NTJ4	Alpha-mannosidase 2C1	MAN2C1 MANA MANA1	0	1	alpha-mannosidosis breast cancer breast carcinoma carcinoma esophageal cancer esophageal carcinoma intellectual disability learning disability post-traumatic stress disorder prostate cancer prostate carcinoma sarcomatoid carcinoma
Q8IWU9	Tryptophan 5-hydroxylase 2	TPH2 NTPH	0	1
O43312	Protein MTSS 1	MTSS1 KIAA0429 MIM	6	1
Q15669	Rho-related GTP-binding protein RhoH	RHOH ARHH TTF	0	1
O60762	Dolichol-phosphate mannosyltransferase subunit 1	DPM1	0	1	Duchenne muscular dystrophy antithrombin III deficiency autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 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 capillary disease cavernous hemangioma chorioangioma congenital disorder of glycosylation Ie congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy glomus tumor hemangioma hereditary hemorrhagic telangiectasia histiocytoid hemangioma intramuscular hemangioma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lymphangioma microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 nonsyndromic congenital nail disorder 9 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 oculopharyngeal muscular dystrophy patent ductus arteriosus protein C deficiency protein S deficiency rippling muscle disease 2 telangiectasis thrombophilia
Q9NYL9	Tropomodulin-3	TMOD3	1	1
Q9H2V7	Protein spinster homolog 1	SPNS1 SPIN1	0	1
Q15386	Ubiquitin-protein ligase E3C	UBE3C KIAA0010 KIAA10	1	1
Q8NGJ3	Olfactory receptor 52E1	OR52E1 OR52E1P	2	1
A6NKD2	Testis-specific Y-encoded protein 2	TSPY2 TSPYQ1	0	1
Q9NVA2	Septin-11	SEPTIN11 SEPT11	1	1
Q7L2H7	Eukaryotic translation initiation factor 3 subunit M	EIF3M HFLB5 PCID1	2	1
Q9UGQ3	Solute carrier family 2, facilitated glucose transporter member 6	SLC2A6 GLUT6	1	1
O15258	Protein RER1	RER1	0	1
Q8IYK8	GTP-binding protein REM 2	REM2	0	1
Q9NQE9	Adenosine 5'-monophosphoramidase HINT3	HINT3	0	1

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