GlyCosmos Portal

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9UNH7	Sorting nexin-6	SNX6	0	1
Q9UNI1	Chymotrypsin-like elastase family member 1	CELA1 ELA1	2	0
Q9UNK4	Group IID secretory phospholipase A2	PLA2G2D SPLASH	1	0	Down syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascending cholangitis atherosclerosis breast cancer cancer cholangitis chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease embryoma large intestine cancer primary sclerosing cholangitis sclerosing cholangitis suppurative cholangitis
Q9UNL2	Translocon-associated protein subunit gamma	SSR3 TRAPG	0	1
Q9UNL4	Inhibitor of growth protein 4	ING4	0	1
Q9UNM6	26S proteasome non-ATPase regulatory subunit 13	PSMD13	0	1
Q9UNN5	FAS-associated factor 1	FAF1 UBXD12 UBXN3A	3	2
Q9UNN8	Endothelial protein C receptor	PROCR EPCR	4	14
Q9UNP4	Lactosylceramide alpha-2,3-sialyltransferase	ST3GAL5 SIAT9	3	2	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Rett syndrome SPOAN syndrome Troyer syndrome Unverricht-Lundborg syndrome agnosia arthritis arthropathy blepharospasm blindness cerebral palsy congenital nystagmus developmental and epileptic encephalopathy 36 dissociated nystagmus dystonia early myoclonic encephalopathy endocrine exophthalmos focal hand dystonia hemiplegia hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer locked-in syndrome microcephaly optic atrophy paroxysmal nonkinesigenic dyskinesia 1 paroxysmal nonkinesigenic dyskinesia 2 pathologic nystagmus quadriplegia salt and pepper syndrome sensorineural hearing loss spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus status epilepticus stereotypic movement disorder syndromic X-linked intellectual disability 94 thromboangiitis obliterans trichohepatoenteric syndrome 1 trichohepatoenteric syndrome visual epilepsy
Q9UNP9	Peptidyl-prolyl cis-trans isomerase E	PPIE CYP33	4	2
Q9UNQ0	Broad substrate specificity ATP-binding cassette transporter ABCG2	ABCG2 ABCP BCRP BCRP1 MXR	1	0
Q9UNQ2	Probable dimethyladenosine transferase	DIMT1 DIMT1L	3	1
Q9UNS2	COP9 signalosome complex subunit 3	COPS3 CSN3	1	1
Q9UNW1	Multiple inositol polyphosphate phosphatase 1	MINPP1 MIPP	7	15	actinic keratosis cancer carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer head and neck cancer large intestine cancer multiple myeloma nodular goiter papillary adenocarcinoma papillary renal cell carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease spinal cord disease thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma
Q9UNW8	Probable G-protein coupled receptor 132	GPR132 G2A	1	0
Q9UNW9	RNA-binding protein Nova-2	NOVA2 ANOVA NOVA3	0	1
Q9UNX3	Ribosomal protein uL24-like	RPL26L1 RPL26P1	0	1
Q9UNX4	WD repeat-containing protein 3	WDR3	2	1
Q9UNY4	Transcription termination factor 2	TTF2	1	2
Q9UNZ2	NSFL1 cofactor p47	NSFL1C UBXN2C	0	1
Q9UNZ5	Leydig cell tumor 10 kDa protein homolog	C19orf53	0	1
Q9UP38	Frizzled-1	FZD1	4	3
Q9UP52	Transferrin receptor protein 2	TFR2	4	0
Q9UP79	A disintegrin and metalloproteinase with thrombospondin motifs 8	ADAMTS8 METH2	6	1
Q9UP83	Conserved oligomeric Golgi complex subunit 5	COG5 GOLTC1 GTC90	1	2	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Cauda equina syndrome Friedreich ataxia Laron syndrome Pick's disease Reye syndrome achondroplasia agnosia arthritis arthropathy atrial fibrillation cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIi congenital disorder of glycosylation coronary artery disease cryptorchidism developmental coordination disorder epilepsy hypertropia intellectual disability learning disability leiomyoma mechanical strabismus microcephaly myofibroma neurogenic bladder oligohydramnios ophthalmoplegia osteoarthritis placental insufficiency sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 uterine fibroid visual epilepsy

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