GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **16876 - 16900** 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
A0A7I2V3I5	Laminin subunit beta 1	LAMB1	Homo sapiens (human)	2	0
A0A0G2R0S6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9H2E1	Neuropilin	NRP1	Homo sapiens (human)	2	0
Q9UKF5	Disintegrin and metalloproteinase domain-containing protein 29	ADAM29	Homo sapiens (human)	9	0
Q86UN6	A-kinase anchor protein 14	AKAP14 AKAP28	Homo sapiens (human)	0	1
F6KS19	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q709C8	Intermembrane lipid transfer protein VPS13C	VPS13C KIAA1421	Homo sapiens (human)	2	4
A0A2P0W8F8	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
A0A090MF30	HLA class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P00751	Complement factor B	CFB BF BFD	Homo sapiens (human)	7	83
A0A288QRR9	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8NGN0	Olfactory receptor 4D5	OR4D5	Homo sapiens (human)	1	0
Q9H0U4	Ras-related protein Rab-1B	RAB1B	Homo sapiens (human)	0	1
P19784	Casein kinase II subunit alpha'	CSNK2A2 CK2A2	Homo sapiens (human)	2	1
H3BSK5	Signal regulatory protein beta 1 (Fragment)	SIRPB1	Homo sapiens (human)	2	0
P62861	Ubiquitin-like FUBI-ribosomal protein eS30 fusion protein	FAU	Homo sapiens (human)	0	1
Q15942	Zyxin	ZYX	Homo sapiens (human)	24	3
Q8NGH5	Olfactory receptor 56A1	OR56A1	Homo sapiens (human)	3	0
Q9NQC7	Ubiquitin carboxyl-terminal hydrolase CYLD	CYLD CYLD1 KIAA0849	Homo sapiens (human)	0	1
B5A929	Soluble MET variant 1	MET	Homo sapiens (human)	5	0
E5RGB0	Clusterin (Fragment)	CLU	Homo sapiens (human)	2	0
R4MS56	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q96KG7	Multiple epidermal growth factor-like domains protein 10	MEGF10 KIAA1780	Homo sapiens (human)	5	0
P23786	Carnitine O-palmitoyltransferase 2, mitochondrial	CPT2 CPT1	Homo sapiens (human)	0	1	Chanarin-Dorfman syndrome Meckel syndrome Pearson syndrome Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis attention deficit hyperactivity disorder autosomal dominant polycystic kidney disease beta thalassemia brain disease brain edema breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency carnitine palmitoyltransferase II deficiency cataract chronic fatigue syndrome chronic kidney disease clubfoot colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy essential thrombocythemia familial hyperlipidemia familial periodic paralysis fibromyalgia glycogen storage disease II glycogen storage disease V hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hydronephrosis hyperglycemia hypertrophic cardiomyopathy hypoglycemia influenza isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer liver cancer liver cirrhosis medium chain acyl-CoA dehydrogenase deficiency microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency myelitis myelodysplastic syndrome myocardial infarction myoglobinuria myopathy myositis neurogenic arthropathy neuroleptic malignant syndrome obesity ovarian cancer pancytopenia placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma pseudosarcomatous fibromatosis psoriatic arthritis sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction status epilepticus steatotic liver disease systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency viral infectious disease visual epilepsy
P54920	Alpha-soluble NSF attachment protein	NAPA SNAPA	Homo sapiens (human)	1	1

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