GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96FN4	Copine-2	CPNE2	0	1
O75131	Copine-3	CPNE3 CPN3 KIAA0636	2	2
Q96A23	Copine-4	CPNE4	0	1
Q8IYJ1	Copine-9	CPNE9	2	1
Q8IVL8	Carboxypeptidase O	CPO	4	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 DiGeorge syndrome Pick's disease Reye syndrome Van der Woude syndrome cerebral degeneration colorectal cancer colorectal carcinoma craniosynostosis hereditary coproporphyria large intestine cancer melorheostosis velocardiofacial syndrome
P36551	Oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial	CPOX CPO CPX	1	2
Q9BRF8	Serine/threonine-protein phosphatase CPPED1	CPPED1 CSTP1	0	1
Q9Y646	Carboxypeptidase Q	CPQ LCH1 PGCP	5	83
P31327	Carbamoyl-phosphate synthase [ammonia], mitochondrial	CPS1	7	5
Q10570	Cleavage and polyadenylation specificity factor subunit 1	CPSF1 CPSF160	1	2
Q9P2I0	Cleavage and polyadenylation specificity factor subunit 2	CPSF2 CPSF100 KIAA1367	1	1
Q9UKF6	Cleavage and polyadenylation specificity factor subunit 3	CPSF3 CPSF73	0	1
O95639	Cleavage and polyadenylation specificity factor subunit 4	CPSF4 CPSF30 NAR NEB1	1	2
Q16630	Cleavage and polyadenylation specificity factor subunit 6	CPSF6 CFIM68	0	1
Q8N684	Cleavage and polyadenylation specificity factor subunit 7	CPSF7	3	1
P50416	Carnitine O-palmitoyltransferase 1, liver isoform	CPT1A CPT1	3	1	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 D-bifunctional protein deficiency Niemann-Pick disease type C1 Niemann-Pick disease Pearson syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction alcoholic hepatitis alveolar rhabdomyosarcoma amnestic disorder beta thalassemia breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency cataract 4 multiple types cerebral degeneration chronic fatigue syndrome chronic kidney disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential thrombocythemia familial hyperlipidemia familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease isolated elevated serum creatine phosphokinase levels large intestine cancer liver cancer liver carcinoma liver cirrhosis lymphangioleiomyomatosis major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia osteoporosis placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis renal tubular acidosis retrograde amnesia sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction skin melanoma speech disorder steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency visual epilepsy
P23786	Carnitine O-palmitoyltransferase 2, mitochondrial	CPT2 CPT1	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
Q5TA50	Ceramide-1-phosphate transfer protein	CPTP GLTPD1	0	1	acute pancreatitis pancreatitis
Q9H3G5	Probable serine carboxypeptidase CPVL	CPVL VLP	5	109
C9JLV0	Carboxypeptidase (Fragment)	CPVL	1	0
H7C0X5	Carboxypeptidase vitellogenic like (Fragment)	CPVL	1	0
O75225	Carboxypeptidase (Fragment)	CPVL	1	0
Q75MM4	Uncharacterized protein CPVL (Fragment)	CPVL	1	0
C9JI22	Carboxypeptidase (Fragment)	CPVL	1	0
Q96SM3	Probable carboxypeptidase X1	CPXM1 CPX1 CPXM	8	22

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