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 **5576 - 5600** 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
Q86WD7	Serpin A9	SERPINA9 GCET1 SERPINA11	Homo sapiens (human)	2	0
P25205	DNA replication licensing factor MCM3	MCM3	Homo sapiens (human)	2	1
Q8WU20	Fibroblast growth factor receptor substrate 2	FRS2	Homo sapiens (human)	2	1
P03956	Interstitial collagenase	MMP1 CLG	Homo sapiens (human)	2	48
Q53XC6	Legumain	LGMN	Homo sapiens (human)	2	0
Q15022	Polycomb protein SUZ12	SUZ12 CHET9 JJAZ1 KIAA0160	Homo sapiens (human)	2	2
Q7LFL8	CXXC-type zinc finger protein 5	CXXC5	Homo sapiens (human)	2	1
Q9H2B4	Sulfate anion transporter 1	SLC26A1 SAT1	Homo sapiens (human)	2	0
Q8TE54	Anion exchange transporter	SLC26A7 SUT2	Homo sapiens (human)	2	3
Q5VWI1	Transcription elongation regulator 1-like protein	TCERG1L	Homo sapiens (human)	2	1
Q0VF49	Uncharacterized protein KIAA2012	KIAA2012	Homo sapiens (human)	2	2
Q13151	Heterogeneous nuclear ribonucleoprotein A0	HNRNPA0 HNRPA0	Homo sapiens (human)	2	2
O95389	Cellular communication network factor 6	CCN6 WISP3	Homo sapiens (human)	2	0
P58400	Neurexin-1-beta	NRXN1	Homo sapiens (human)	2	0
Q96A28	SLAM family member 9	SLAMF9 CD2F10	Homo sapiens (human)	2	0
Q9UQ84	Exonuclease 1	EXO1 EXOI HEX1	Homo sapiens (human)	2	1
Q5TZA2	Rootletin	CROCC KIAA0445	Homo sapiens (human)	2	1
Q9H772	Gremlin-2	GREM2 CKTSF1B2 DAND3 PRDC	Homo sapiens (human)	2	0
O95149	Snurportin-1	SNUPN RNUT1 SPN1	Homo sapiens (human)	2	1
Q8IYJ1	Copine-9	CPNE9	Homo sapiens (human)	2	1
V9HWI3	Cathepsin D	HEL-S-130P CTSD	Homo sapiens (human)	2	0
Q6P1L5	Protein FAM117B	FAM117B ALS2CR13	Homo sapiens (human)	2	2
P48167	Glycine receptor subunit beta	GLRB	Homo sapiens (human)	2	1
X5D7P3	Seizure related 6-like protein 2 isoform B (Fragment)	SEZ6L2	Homo sapiens (human)	2	0
P09622	Dihydrolipoyl dehydrogenase, mitochondrial	DLD GCSL LAD PHE3	Homo sapiens (human)	2	2	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Friedreich ataxia Glanzmann's thrombasthenia Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute monocytic leukemia acute myocardial infarction adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma adult fibrosarcoma alexia alternating hemiplegia of childhood amyotrophic lateral sclerosis antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative autistic disorder autonomic neuropathy bacterial sepsis benign mesothelioma brain disease brain infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia choriocarcinoma chromophobe renal cell carcinoma chronic monocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communication disorder congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc congenital disorder of glycosylation congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma cutaneous mastocytosis dementia depressive disorder diabetes mellitus diabetic ketoacidosis diffuse cutaneous mastocytosis disease of metabolism dyslexia dysthymic disorder dystonia embryoma endomyocardial fibrosis epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial hypertrophic cardiomyopathy fibrosarcoma follicular adenoma fragile X syndrome frontotemporal dementia giant cell glioblastoma glioblastoma granular cell carcinoma gray platelet syndrome hepatic coma hepatic encephalopathy hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypertensive retinopathy hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intermittent claudication islet cell tumor lactic acidosis language disorder large intestine cancer learning disability leukemia leukocyte adhesion deficiency 2 leukocyte adhesion deficiency 3 leukocyte adhesion deficiency lissencephaly liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lymphoid leukemia major depressive disorder malignant mesothelioma maple syrup urine disease mastocytosis melancholic depression methemoglobinemia microcephaly microcystic adenoma monocytic leukemia multiple myeloma multiple sclerosis myeloid leukemia myocardial infarction nervous system disease neuroblastoma neurotic disorder obsolete melancholia pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma periodontitis peripheral vascular disease placenta cancer platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 posterior myocardial infarction primary immunodeficiency disease progressive muscular atrophy prostate cancer prostate carcinoma protein C deficiency protein S deficiency pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency qualitative platelet defect renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia short chain acyl-CoA dehydrogenase deficiency silent myocardial infarction stomach cancer stomach carcinoma stuttering sulfhemoglobinemia thrombophilia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urea cycle disorder urticaria pigmentosa varicose veins vascular disease viral infectious disease visual epilepsy

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