GlyCosmos Portal

Displaying entries **3401 - 3425** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
P34949	Mannose-6-phosphate isomerase	MPI PMI1	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 Pick's disease Reye syndrome Zollinger-Ellison syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency anxiety disorder arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant cerebellar ataxia autosomal recessive hypercholesterolemia autosomal recessive polycystic kidney disease blindness blood coagulation disease campomelic dysplasia cancer cardiovascular system disease celiac disease central nervous system cancer cerebral degeneration chronic kidney disease congenital disorder of glycosylation Ia congenital disorder of glycosylation Ib congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congestive heart failure coronary artery disease coronary thrombosis craniometaphyseal dysplasia cryptococcosis cystic fibrosis developmental and epileptic encephalopathy 36 diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy dry eye syndrome egg allergy elephantiasis embryoma epilepsy essential hypertension familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 gallbladder disease generalized anxiety disorder gliosarcoma heart disease hepatitis B high grade glioma hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia laryngeal disease liver cirrhosis liver disease lymphedema marasmus mixed glioma myocardial infarction neurotic disorder nutmeg liver obsolete inherited blood coagulation disease phobic disorder placental insufficiency polycystic kidney disease 4 post-traumatic stress disorder postpartum depression protein C deficiency protein S deficiency protein-losing enteropathy schizophrenia silent myocardial infarction spinocerebellar ataxia type 6 steatotic liver disease thrombocytopenia thrombophilia tracheal disease tropical sprue type 2 diabetes mellitus visual epilepsy xerophthalmia
P0C5J1	Putative protein N-methyltransferase FAM86B2	FAM86B2	1
Q6ZS17	Rho family-interacting cell polarization regulator 1	RIPOR1 FAM65A KIAA1930	1
P13647	Keratin, type II cytoskeletal 5	KRT5	1
O95707	Ribonuclease P protein subunit p29	POP4 RPP29	1
Q6N063	2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2	OGFOD2	1
Q9NTK5	Obg-like ATPase 1	OLA1 GTPBP9	1
Q9Y446	Plakophilin-3	PKP3	1
Q8NBH2	Kyphoscoliosis peptidase	KY	1
Q9Y6U3	Scinderin	SCIN KIAA1905	1
Q9NX00	Transmembrane protein 160	TMEM160	1
Q13596	Sorting nexin-1	SNX1	1
Q86UD3	E3 ubiquitin-protein ligase MARCHF3	MARCHF3 MARCH3 RNF173	1
O94776	Metastasis-associated protein MTA2	MTA2 MTA1L1 PID	1
Q3KR16	Pleckstrin homology domain-containing family G member 6	PLEKHG6	1
Q8TDN1	Potassium voltage-gated channel subfamily G member 4	KCNG4 KCNG3	1
Q9H0S4	Probable ATP-dependent RNA helicase DDX47	DDX47	1
Q9UNZ5	Leydig cell tumor 10 kDa protein homolog	C19orf53	1
Q9UL16	Cilia- and flagella-associated protein 45	CFAP45 CCDC19 NESG1	1
Q13670	Putative postmeiotic segregation increased 2-like protein 11	PMS2P11 PMS2L11 PMSR6	1
Q13882	Protein-tyrosine kinase 6	PTK6 BRK	1
Q9NVI1	Fanconi anemia group I protein	FANCI KIAA1794	1
Q9BYM8	RanBP-type and C3HC4-type zinc finger-containing protein 1	RBCK1 C20orf18 RNF54 UBCE7IP3 XAP3 XAP4	1
Q9H3R5	Centromere protein H	CENPH ICEN35	1
Q9NX65	Zinc finger and SCAN domain-containing protein 32	ZSCAN32 ZNF434	1

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