GlyCosmos Portal

Displaying entries **5126 - 5150** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9Y5I2	Protocadherin alpha-10	PCDHA10 CNRS8	3	0
Q9Y5I3	Protocadherin alpha-1	PCDHA1	3	0
Q9HC56	Protocadherin-9	PCDH9	15	22
O95206	Protocadherin-8	PCDH8	3	0
O60245	Protocadherin-7	PCDH7 BHPCDH	9	3
Q8N6Y1	Protocadherin-20	PCDH20 PCDH13	8	2
Q8TAB3	Protocadherin-19	PCDH19 KIAA1313	6	1
Q9HCL0	Protocadherin-18	PCDH18 KIAA1562	6	0
O14917	Protocadherin-17	PCDH17 PCDH68 PCH68	7	4
Q96QU1	Protocadherin-15	PCDH15 USH1F	13	0
Q9NPG4	Protocadherin-12	PCDH12	8	2
Q9BZA8	Protocadherin-11 Y-linked	PCDH11Y PCDH11 PCDH22 PCDHY	7	1
Q9BZA7	Protocadherin-11 X-linked	PCDH11X KIAA1326 PCDH11 PCDHX	9	4
Q9P2E7	Protocadherin-10	PCDH10 KIAA1400	2	0
Q08174	Protocadherin-1	PCDH1	7	9
P05166	Propionyl-CoA carboxylase beta chain, mitochondrial	PCCB	1	1	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis anemia anxiety disorder cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy generalized anxiety disorder granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis schizophrenia severe congenital neutropenia sick sinus syndrome thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
P05165	Propionyl-CoA carboxylase alpha chain, mitochondrial	PCCA	2	1	Laron syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis anemia cardiomyopathy cerebral degeneration colorectal cancer colorectal carcinoma cribriform carcinoma dermatitis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dystonia endomyocardial fibrosis epilepsy granular cell carcinoma hypertrophic cardiomyopathy hypoglycemia intellectual disability lactic acidosis large intestine cancer learning disability macrocytic anemia neutropenia nicotine dependence obsolete constipation osteoporosis pancreatitis pancytopenia pontocerebellar hypoplasia type 2D propionic acidemia psoriatic arthritis refractive error severe congenital neutropenia sick sinus syndrome stomach cancer stomach carcinoma thrombocytopenia tubular adenocarcinoma urea cycle disorder visual epilepsy
P57723	Poly(rC)-binding protein 4	PCBP4	0	1
P57721	Poly(rC)-binding protein 3	PCBP3 PCBP3-OT1 PCBP3OT	0	1
B4DLC0	cDNA FLJ58476, highly similar to Poly(rC)-binding protein 2	PCBP2	0	1
Q15366	Poly(rC)-binding protein 2	PCBP2	3	3
F8VRH0	Poly(rC) binding protein 2 (Fragment)	PCBP2	0	1
Q15365	Poly(rC)-binding protein 1	PCBP1	9	4
P11498	Pyruvate carboxylase, mitochondrial	PC	1	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 B-cell lymphoma Burkitt lymphoma Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Pick's disease Reye syndrome Sjogren's syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction adult fibrosarcoma alcohol dependence alcohol use disorder allergic asthma antiphospholipid syndrome antithrombin III deficiency anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis attention deficit hyperactivity disorder autistic disorder autoimmune polyendocrine syndrome autosomal dominant familial periodic fever bacterial sepsis beta thalassemia bipolar disorder blood coagulation disease breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma colitis congenital afibrinogenemia coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis disseminated intravascular coagulation embryoma enterobiasis epilepsy essential hypertension factor V deficiency factor VII deficiency familial hyperlipidemia fibrosarcoma gallbladder cancer gallbladder carcinoma gastroenteritis generalized anxiety disorder glomerulonephritis heart disease hemoglobin H disease hepatitis hepatocellular carcinoma holocarboxylase synthetase deficiency hyperglycemia hyperhomocysteinemia hyperlysinemia hypertension hyperthyroidism hyperuricemia hypoglycemia ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease intellectual disability intestinal schistosomiasis intracranial sinus thrombosis ischemic colitis keratoconjunctivitis sicca kidney disease kwashiorkor lactic acidosis learning disability leukodystrophy liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lupus erythematosus lymphoma malignant exocrine pancreas neoplasm marasmus melanoma multiple sclerosis myocardial infarction nephritis nephrosis non-Hodgkin lymphoma nutrition disease obesity obsolete inherited blood coagulation disease obsolete ymphosarcoma papillary adenocarcinoma papillary renal cell carcinoma periventricular leukomalacia phobic disorder portal vein thrombosis protein C deficiency protein S deficiency protein-energy malnutrition purpura fulminans pyoureter pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal tubular acidosis reticulosarcoma schistosomiasis silent myocardial infarction skin melanoma steatotic liver disease synovial sarcoma systemic lupus erythematosus thalassemia thrombophilia thyroid gland papillary carcinoma thyrotoxicosis trichinosis tuberculosis type 2 diabetes mellitus urea cycle disorder visual epilepsy vitamin K deficiency bleeding
Q96AQ6	Pre-B-cell leukemia transcription factor-interacting protein 1	PBXIP1 HPIP	2	14

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