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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q96M83	Coiled-coil domain-containing protein 7	CCDC7 BIOT2 C10orf68	2	1
H0Y5N9	Collagen type XII alpha 1 chain (Fragment)	COL12A1	2	0
P09871	Complement C1s subcomponent	C1S	2	8
O15552	Free fatty acid receptor 2	FFAR2 FFA2 GPCR43 GPR43	2	0
Q7L014	Probable ATP-dependent RNA helicase DDX46	DDX46 KIAA0801	2	1
A0A494C0K8	Immunoglobulin superfamily member 1	IGSF1	2	0
P58743	Prestin	SLC26A5 PRES	2	0
H0YKJ9	Tetraspanin 3	TSPAN3	2	0
Q13370	cGMP-inhibited 3',5'-cyclic phosphodiesterase 3B	PDE3B	2	1
P43115	Prostaglandin E2 receptor EP3 subtype	PTGER3	2	0
Q92543	Sorting nexin-19	SNX19 KIAA0254	2	1
Q09428	ATP-binding cassette sub-family C member 8	ABCC8 HRINS SUR SUR1	2	0
A8MTI9	Putative serine protease 47	PRSS47P PRSS47	2	0
Q07092	Collagen alpha-1(XVI) chain	COL16A1	2	1
Q8NBK3	Formylglycine-generating enzyme	SUMF1	2	12	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
P10745	Retinol-binding protein 3	RBP3	2	0
Q8NH43	Olfactory receptor 4L1	OR4L1 OR4L2P	2	0
Q8IUB2	WAP four-disulfide core domain protein 3	WFDC3 WAP14	2	0
Q86UW9	Probable E3 ubiquitin-protein ligase DTX2	DTX2 KIAA1528 RNF58	2	3
Q5JZY3	Ephrin type-A receptor 10	EPHA10	2	0
A0A1A7UP97	N-acetylgalactosamine-6-sulfatase	GALNS	2	0
P52961	GPI-linked NAD(P)(+)--arginine ADP-ribosyltransferase 1	ART1	2	0	arthritis arthropathy astigmatism cancer central nervous system cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liver cancer mixed glioma nasopharynx carcinoma nephritis pancreatic cancer pancreatic carcinoma squamous cell carcinoma tongue squamous cell carcinoma tuberculosis
Q6UW88	Epigen	EPGN	2	0
P16118	6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 1	PFKFB1 F6PK PFRX	2	1	Zollinger-Ellison syndrome cancer hyperinsulinism stomach cancer
Q9NXG2	THUMP domain-containing protein 1	THUMPD1	2	1

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