GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
O43242	26S proteasome non-ATPase regulatory subunit 3	PSMD3	4	2
P49796	Regulator of G-protein signaling 3	RGS3	4	1
Q14571	Inositol 1,4,5-trisphosphate receptor type 2	ITPR2	4	9
Q15058	Kinesin-like protein KIF14	KIF14 KIAA0042	4	1
Q8N130	Sodium-dependent phosphate transport protein 2C	SLC34A3 NPT2C NPTIIC	4	0
Q96NU0	Contactin-associated protein-like 3B	CNTNAP3B CASPR3B	4	4
Q8TEQ8	GPI ethanolamine phosphate transferase 3	PIGO	4	2	Cogan syndrome Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome absence epilepsy blepharospasm capillary disease childhood absence epilepsy cleft palate colorectal cancer colorectal carcinoma craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability monocular esotropia nonepidermolytic palmoplantar keratoderma oligohydramnios palmoplantar keratosis scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis visual epilepsy
P55291	Cadherin-15	CDH15 CDH14 CDH3	4	0
P0DQD5	Neuropeptide Y receptor type 4-2	NPY4R2	4	0
P78316	Nucleolar protein 14	NOP14 C4orf9 NOL14	4	1
Q96GX1	Tectonic-2	TCTN2 C12orf38 TECT2	4	0
P30260	Cell division cycle protein 27 homolog	CDC27 ANAPC3 D0S1430E D17S978E	4	3
P54762	Ephrin type-B receptor 1	EPHB1 ELK EPHT2 HEK6 NET	4	1
O14791	Apolipoprotein L1	APOL1 APOL	4	3
Q9BYT9	Anoctamin-3	ANO3 C11orf25 TMEM16C	4	0
Q96EG1	Arylsulfatase G	ARSG KIAA1001	4	0	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome type 3A Usher syndrome anxiety disorder astigmatism blepharospasm blindness cancer cataract cerebellar ataxia cerebellar disease congenital stationary night blindness 1A congenital stationary night blindness depressive disorder dysthymic disorder dystonia embryoma focal dystonia focal hand dystonia generalized anxiety disorder generalized dystonia lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder night blindness obsolete melancholia peripheral retinal degeneration prostate cancer prostate carcinoma retinitis pigmentosa-deafness syndrome schizophrenia scotoma sensorineural hearing loss
Q7Z410	Transmembrane protease serine 9	TMPRSS9	4	0
Q9UNA3	Alpha-1,4-N-acetylglucosaminyltransferase	A4GNT	4	0	adenocarcinoma adenoma cancer cribriform carcinoma embryoma gastric adenocarcinoma gastritis granular cell carcinoma pancreatic cancer pancreatic carcinoma peptic ulcer disease stomach cancer stomach carcinoma tubular adenocarcinoma
Q5JTW2	Centrosomal protein of 78 kDa	CEP78 C9orf81	4	1
Q96DZ1	Endoplasmic reticulum lectin 1	ERLEC1 C2orf30 XTP3TPB	4	4	anorexia nervosa bronchus cancer bronchus carcinoma cancer cholestasis lung benign neoplasm lung cancer lung carcinoma spinal cord disease syringomyelia
O75030	Microphthalmia-associated transcription factor	MITF BHLHE32	4	1
P13674	Prolyl 4-hydroxylase subunit alpha-1	P4HA1 P4HA	4	26
O60566	Mitotic checkpoint serine/threonine-protein kinase BUB1 beta	BUB1B BUBR1 MAD3L SSK1	4	13
Q95IG1	Complement C2 (Fragment)	C2	4	0
Q3KQU3	MAP7 domain-containing protein 1	MAP7D1 KIAA1187 PARCC1 RPRC1	4	1

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