GlyCosmos Portal

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GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **18401 - 18425** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
P02671	Fibrinogen alpha chain	FGA	Homo sapiens (human)	37	19
Q14112	Nidogen-2	NID2	Homo sapiens (human)	37	115
P39060	Collagen alpha-1(XVIII) chain	COL18A1	Homo sapiens (human)	37	21
Q86UK0	Glucosylceramide transporter ABCA12	ABCA12 ABC12	Homo sapiens (human)	37	6
P11279	Lysosome-associated membrane glycoprotein 1	LAMP1	Homo sapiens (human)	37	334
Q6VMQ6	Activating transcription factor 7-interacting protein 1	ATF7IP MCAF MCAF1	Homo sapiens (human)	37	3
Q8TCU4	Centrosome-associated protein ALMS1	ALMS1 KIAA0328	Homo sapiens (human)	39	3
Q9Y6V0	Protein piccolo	PCLO ACZ KIAA0559	Homo sapiens (human)	39	1
P02751	Fibronectin	FN1 FN	Homo sapiens (human)	39	276
Q2KHR3	Glutamine and serine-rich protein 1	QSER1	Homo sapiens (human)	40	3
P52594	Arf-GAP domain and FG repeat-containing protein 1	AGFG1 HRB RAB RIP	Homo sapiens (human)	40	3
Q96PZ7	CUB and sushi domain-containing protein 1	CSMD1 KIAA1890	Homo sapiens (human)	40	0
Q9NXV6	CDKN2A-interacting protein	CDKN2AIP CARF	Homo sapiens (human)	40	4
P27816	Microtubule-associated protein 4	MAP4	Homo sapiens (human)	40	3
Q9NYQ8	Protocadherin Fat 2	FAT2 CDHF8 KIAA0811 MEGF1	Homo sapiens (human)	40	2
Q6MZP7	Protein lin-54 homolog	LIN54 CXCDC1 KIAA2037	Homo sapiens (human)	40	2
Q8WWI1	LIM domain only protein 7	LMO7 FBX20 FBXO20 KIAA0858	Homo sapiens (human)	41	3
Q7Z3K3	Pogo transposable element with ZNF domain	POGZ KIAA0461 SUHW5 ZNF280E ZNF635	Homo sapiens (human)	41	4
Q15652	Probable JmjC domain-containing histone demethylation protein 2C	JMJD1C JHDM2C KIAA1380 TRIP8	Homo sapiens (human)	41	4
P09603	Macrophage colony-stimulating factor 1	CSF1	Homo sapiens (human)	41	7
O75976	Carboxypeptidase D	CPD	Homo sapiens (human)	41	85
Q3T906	N-acetylglucosamine-1-phosphotransferase subunits alpha/beta	GNPTAB GNPTA KIAA1208	Homo sapiens (human)	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	Homo sapiens (human)	42	4
A2VEC9	SCO-spondin	SSPOP KIAA2036 SSPO	Homo sapiens (human)	43	0
Q6V0I7	Protocadherin Fat 4	FAT4 CDHF14 FATJ	Homo sapiens (human)	43	12

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