GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
P02671	Fibrinogen alpha chain	FGA	37	19
Q14112	Nidogen-2	NID2	37	115
P39060	Collagen alpha-1(XVIII) chain	COL18A1	37	21
Q86UK0	Glucosylceramide transporter ABCA12	ABCA12 ABC12	37	6
P11279	Lysosome-associated membrane glycoprotein 1	LAMP1	37	334
Q6VMQ6	Activating transcription factor 7-interacting protein 1	ATF7IP MCAF MCAF1	37	3
Q8TCU4	Centrosome-associated protein ALMS1	ALMS1 KIAA0328	39	3
Q9Y6V0	Protein piccolo	PCLO ACZ KIAA0559	39	1
P02751	Fibronectin	FN1 FN	39	276
Q2KHR3	Glutamine and serine-rich protein 1	QSER1	40	3
P52594	Arf-GAP domain and FG repeat-containing protein 1	AGFG1 HRB RAB RIP	40	3
Q96PZ7	CUB and sushi domain-containing protein 1	CSMD1 KIAA1890	40	0
Q9NXV6	CDKN2A-interacting protein	CDKN2AIP CARF	40	4
P27816	Microtubule-associated protein 4	MAP4	40	3
Q9NYQ8	Protocadherin Fat 2	FAT2 CDHF8 KIAA0811 MEGF1	40	2
Q6MZP7	Protein lin-54 homolog	LIN54 CXCDC1 KIAA2037	40	2
Q8WWI1	LIM domain only protein 7	LMO7 FBX20 FBXO20 KIAA0858	41	3
Q7Z3K3	Pogo transposable element with ZNF domain	POGZ KIAA0461 SUHW5 ZNF280E ZNF635	41	4
Q15652	Probable JmjC domain-containing histone demethylation protein 2C	JMJD1C JHDM2C KIAA1380 TRIP8	41	4
P09603	Macrophage colony-stimulating factor 1	CSF1	41	7
O75976	Carboxypeptidase D	CPD	41	85
Q3T906	N-acetylglucosamine-1-phosphotransferase subunits alpha/beta	GNPTAB GNPTA KIAA1208	42	24	Ebola hemorrhagic fever Fabry disease Laron syndrome Legg-Calve-Perthes disease Scheuermann's disease achondroplasia alexia anemia aortic valve insufficiency arrhythmogenic right ventricular cardiomyopathy autistic disorder cancer capillary hemangioma cardiomyopathy cavernous hemangioma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma clubfoot collecting duct carcinoma congenital central hypoventilation syndrome congestive heart failure corneal dystrophy craniosynostosis disease of metabolism dyslexia embryoma endomyocardial fibrosis enterocele familial hypertrophic cardiomyopathy glycoproteinosis hemangioma hypertrophic cardiomyopathy inguinal hernia intellectual disability keratosis follicularis learning disability lipid storage disease lysosomal storage disease macrocytic anemia megalocornea mixed sleep apnea mongolian spot mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia nonpapillary renal cell carcinoma obstructive sleep apnea omphalocele osteochondrodysplasia papillary renal cell carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinal degeneration retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis sleep apnea spinal cord disease stuttering syringomyelia umbilical hernia
Q9H251	Cadherin-23	CDH23 KIAA1774 KIAA1812	42	4
A2VEC9	SCO-spondin	SSPOP KIAA2036 SSPO	43	0
Q6V0I7	Protocadherin Fat 4	FAT4 CDHF14 FATJ	43	12

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