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 **14851 - 14875** 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
Q86VE9	Serine incorporator 5	SERINC5 C5orf12	Homo sapiens (human)	3	0
Q5QGZ9	C-type lectin domain family 12 member A	CLEC12A CLL1 DCAL2 MICL	Homo sapiens (human)	3	0	Crohn's colitis Crohn's disease Richter's syndrome acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia arthritis arthropathy cancer childhood leukemia chronic fatigue syndrome chronic lymphocytic leukemia chronic myeloid leukemia dermatophytosis embryoma encephalitis encephalomyelitis essential thrombocythemia fungal infectious disease immune system disease inflammatory bowel disease 1 inflammatory bowel disease leukemia lymphoblastic lymphoma lymphocytic choriomeningitis lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma rheumatoid arthritis ulcerative colitis
Q15428	Splicing factor 3A subunit 2	SF3A2 SAP62	Homo sapiens (human)	3	1
F8VV56	CD63 molecule	CD63	Homo sapiens (human)	3	0
P31358	CAMPATH-1 antigen	CD52 CDW52 HE5	Homo sapiens (human)	3	0
P68032	Actin, alpha cardiac muscle 1	ACTC1 ACTC	Homo sapiens (human)	3	2
O60503	Adenylate cyclase type 9	ADCY9 KIAA0520	Homo sapiens (human)	3	3
P78380	Oxidized low-density lipoprotein receptor 1	OLR1 CLEC8A LOX1	Homo sapiens (human)	3	0	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 Cockayne syndrome Kawasaki disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis acute chest syndrome acute myocardial infarction adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation bone osteosarcoma brain stem infarction breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease carpal tunnel syndrome central sleep apnea cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma choriocarcinoma chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma endomyocardial fibrosis essential hypertension familial hypercholesterolemia familial hyperlipidemia gallbladder disease generalized atherosclerosis gestational diabetes giant cell glioblastoma glioblastoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma hyperhomocysteinemia hypertension hypertrophic cardiomyopathy juvenile rheumatoid arthritis keratitis keratoconjunctivitis kidney failure large intestine cancer liver cancer liver disease lung adenocarcinoma lung cancer multiple sclerosis multiple system atrophy myocardial infarction nutmeg liver obesity osteoarthritis osteosarcoma pancreatic cancer pancreatic carcinoma parapsoriasis placenta cancer postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole renal osteodystrophy rheumatoid arthritis seborrheic keratosis sickle cell anemia silent myocardial infarction skin disease transient cerebral ischemia tubular adenocarcinoma type 2 diabetes mellitus vascular disease vertebrobasilar insufficiency
P15382	Potassium voltage-gated channel subfamily E member 1	KCNE1	Homo sapiens (human)	3	0
Q05996	Zona pellucida sperm-binding protein 2	ZP2 ZPA	Homo sapiens (human)	3	0
Q9P2D0	Inhibitor of Bruton tyrosine kinase	IBTK BTKI KIAA1417	Homo sapiens (human)	3	3
Q969Y0	NXPE family member 3	NXPE3 FAM55C	Homo sapiens (human)	3	0
A6NHS7	MANSC domain-containing protein 4	MANSC4	Homo sapiens (human)	3	0
Q95IC0	MHC class I chain-related protein A (Fragment)	MICA	Homo sapiens (human)	3	0
O94761	ATP-dependent DNA helicase Q4	RECQL4 RECQ4	Homo sapiens (human)	3	1
P46695	Radiation-inducible immediate-early gene IEX-1	IER3 DIF2 IEX1 PRG1	Homo sapiens (human)	3	1
Q8WTT0	C-type lectin domain family 4 member C	CLEC4C BDCA2 CLECSF11 CLECSF7 DLEC HECL	Homo sapiens (human)	3	0
P01127	Platelet-derived growth factor subunit B	PDGFB PDGF2 SIS	Homo sapiens (human)	3	6
Q8IYG2	Glypican-3	GPC3	Homo sapiens (human)	3	0
A0A7D9C115	MHC Class I chain-related protein	MICA	Homo sapiens (human)	3	0
H3BS21	Haptoglobin (Fragment)	HP	Homo sapiens (human)	3	0
O15085	Rho guanine nucleotide exchange factor 11	ARHGEF11 KIAA0380	Homo sapiens (human)	3	2
B4E2S7	cDNA FLJ58780, highly similar to Homo sapiens lysosomal-associated membrane protein 2 (LAMP2), transcript variant LAMP2B, mRNA	LAMP2	Homo sapiens (human)	3	0
Q9ULQ1	Two pore channel protein 1	TPCN1 KIAA1169 TPC1	Homo sapiens (human)	3	0
P13232	Interleukin-7	IL7	Homo sapiens (human)	3	0

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