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 **1801 - 1825** 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
Q9HB15	Potassium channel subfamily K member 12	KCNK12	Homo sapiens (human)	1	0
Q96PV7	Protein FAM193B	FAM193B IRIZIO KIAA1931	Homo sapiens (human)	0	1
Q9BPX5	Actin-related protein 2/3 complex subunit 5-like protein	ARPC5L	Homo sapiens (human)	1	1
A6NGU5	Putative glutathione hydrolase 3 proenzyme	GGT3P GGT3	Homo sapiens (human)	9	5
Q07955	Serine/arginine-rich splicing factor 1	SRSF1 ASF SF2 SF2P33 SFRS1	Homo sapiens (human)	0	1
Q9UHF4	Interleukin-20 receptor subunit alpha	IL20RA	Homo sapiens (human)	6	0
D3U3Q9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q14896	Myosin-binding protein C, cardiac-type	MYBPC3	Homo sapiens (human)	3	1
A0A182DWH8	Selenoprotein P (Fragment)	SELENOP	Homo sapiens (human)	3	0
Q6GPH4	XIAP-associated factor 1	XAF1 BIRC4BP XIAPAF1	Homo sapiens (human)	0	1
O95243	Methyl-CpG-binding domain protein 4	MBD4 MED1	Homo sapiens (human)	1	2	Evans' syndrome Hantavirus hemorrhagic fever with renal syndrome Marinesco-Sjogren syndrome abdominal aortic aneurysm achromatopsia acquired color blindness acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma aortic aneurysm autistic disorder autoimmune thrombocytopenic purpura biliary atresia bladder carcinoma blue color blindness breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma cribriform carcinoma disease of metabolism embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma follicular adenoma gastrointestinal system cancer gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microcystic adenoma mixed glioma osteomyelitis papillary adenoma primary cerebellar degeneration red color blindness red-green color blindness rheumatoid arthritis sarcomatoid carcinoma scleroderma stomach cancer stomach carcinoma systemic lupus erythematosus systemic scleroderma temporal arteritis thrombocytopenia due to platelet alloimmunization thrombocytopenia tubular adenocarcinoma urinary bladder cancer uterine corpus cancer uveal melanoma
P11310	Medium-chain specific acyl-CoA dehydrogenase, mitochondrial	ACADM	Homo sapiens (human)	1	1	D-bifunctional protein deficiency Reye syndrome brain edema breast cancer breast carcinoma cancer carnitine palmitoyltransferase I deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congestive heart failure cystinuria diarrhea disease of metabolism distal arthrogryposis epilepsy familial periodic paralysis galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis hydrocephalus hypoglycemia hypoglycemic coma inherited metabolic disorder isolated elevated serum creatine phosphokinase levels lactic acidosis large intestine cancer liver disease long QT syndrome medium chain acyl-CoA dehydrogenase deficiency metabolic dysfunction-associated steatotic liver disease myopathy neuroblastoma neurodegenerative disease nonpapillary renal cell carcinoma obesity papillary renal cell carcinoma perinatal necrotizing enterocolitis phenylketonuria pseudosarcomatous fibromatosis psoriatic arthritis renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma sick sinus syndrome steatotic liver disease sudden infant death syndrome systemic primary carnitine deficiency disease urea cycle disorder visual epilepsy
K7WPE6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9UJQ4	Sal-like protein 4	SALL4 ZNF797	Homo sapiens (human)	2	1
O60412	Olfactory receptor 7C2	OR7C2 OR7C3	Homo sapiens (human)	1	0
P40123	Adenylyl cyclase-associated protein 2	CAP2	Homo sapiens (human)	0	1
D6ML86	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P60153	Inactive ribonuclease-like protein 9	RNASE9	Homo sapiens (human)	2	0
A8MZA4	Golgin subfamily A member 6-like protein 6	GOLGA6L6	Homo sapiens (human)	1	1
Q14765	Signal transducer and activator of transcription 4	STAT4	Homo sapiens (human)	3	1
Q96LB8	Peptidoglycan recognition protein 4	PGLYRP4 PGRPIB	Homo sapiens (human)	5	0
P35219	Carbonic anhydrase-related protein	CA8 CALS	Homo sapiens (human)	0	1
Q8NH51	Olfactory receptor 8K3	OR8K3	Homo sapiens (human)	1	0
Q13115	Dual specificity protein phosphatase 4	DUSP4 MKP2 VH2	Homo sapiens (human)	0	1
Q6SPF0	Sterile alpha motif domain-containing protein 1	SAMD1	Homo sapiens (human)	1	1

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