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 **14901 - 14925** of **18496** in total

« First

‹ Prev

…

593

594

595

596

597

598

599

600

601

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol ▼	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P68104	Elongation factor 1-alpha 1	EEF1A1 EEF1A EF1A LENG7	Homo sapiens (human)	8	8
Q15075	Early endosome antigen 1	EEA1 ZFYVE2	Homo sapiens (human)	4	2
P24530	Endothelin receptor type B	EDNRB ETRB	Homo sapiens (human)	1	0
P25101	Endothelin-1 receptor	EDNRA ETA ETRA	Homo sapiens (human)	4	3
P20800	Endothelin-2	EDN2	Homo sapiens (human)	5	1
P05305	Endothelin-1	EDN1	Homo sapiens (human)	2	1
O43854	EGF-like repeat and discoidin I-like domain-containing protein 3	EDIL3 DEL1	Homo sapiens (human)	7	3
O60869	Endothelial differentiation-related factor 1	EDF1	Homo sapiens (human)	0	1
Q9BZQ6	ER degradation-enhancing alpha-mannosidase-like protein 3	EDEM3 C1orf22	Homo sapiens (human)	8	11	hepatitis C prostate cancer prostate carcinoma
Q9BV94	ER degradation-enhancing alpha-mannosidase-like protein 2	EDEM2 C20orf31 C20orf49	Homo sapiens (human)	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 Pick's disease Reye syndrome cerebral degeneration leiomyoma myofibroma schizophrenia uterine fibroid
Q92611	ER degradation-enhancing alpha-mannosidase-like protein 1	EDEM1 EDEM KIAA0212	Homo sapiens (human)	7	7	depressive disorder hepatitis C major depressive disorder melancholic depression melanoma neurotic disorder obsolete melancholia skin melanoma
A0A1B0GTR0	Epididymal protein 13	EDDM13	Homo sapiens (human)	1	0
Q6P2E9	Enhancer of mRNA-decapping protein 4	EDC4 HEDLS	Homo sapiens (human)	0	1
Q96F86	Enhancer of mRNA-decapping protein 3	EDC3 LSM16 YJDC YJEFN2	Homo sapiens (human)	2	1
Q9UNE0	Tumor necrosis factor receptor superfamily member EDAR	EDAR DL	Homo sapiens (human)	2	1
Q9HAV5	Tumor necrosis factor receptor superfamily member 27	EDA2R TNFRSF27 XEDAR	Homo sapiens (human)	1	1
Q92838	Ectodysplasin-A	EDA ED1 EDA2	Homo sapiens (human)	2	0
Q9H8V3	Protein ECT2	ECT2	Homo sapiens (human)	3	2
Q19T08	Endothelial cell-specific chemotaxis regulator	ECSCR ECSM2	Homo sapiens (human)	3	3
Q5VYK3	Proteasome adapter and scaffold protein ECM29	ECPAS ECM29 KIAA0368	Homo sapiens (human)	10	6
O94769	Extracellular matrix protein 2	ECM2	Homo sapiens (human)	6	21
Q16610	Extracellular matrix protein 1	ECM1	Homo sapiens (human)	23	47
O75521	Enoyl-CoA delta isomerase 2	ECI2 DRS1 HCA88 PECI	Homo sapiens (human)	0	1	aplastic anemia paroxysmal nocturnal hemoglobinuria prostate cancer prostate carcinoma pure red-cell aplasia
P42126	Enoyl-CoA delta isomerase 1, mitochondrial	ECI1 DCI	Homo sapiens (human)	0	1	achalasia carcinoma congenital diaphragmatic hernia dilated cardiomyopathy 1A dilated cardiomyopathy esophagitis gastroesophageal reflux disease hiatus hernia megaesophagus peptic esophagitis
P30084	Enoyl-CoA hydratase, mitochondrial	ECHS1	Homo sapiens (human)	1	1	3-methylglutaconic aciduria Balo concentric sclerosis Hailey-Hailey disease Leigh disease Rothmund-Thomson syndrome adrenoleukodystrophy alcohol dependence alcohol use disorder anemia autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB breast cancer breast carcinoma cancer cardiomyopathy central nervous system disease childhood onset GLUT1 deficiency syndrome 2 chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy congenital nystagmus congenital ptosis cutis laxa disease of metabolism dissociated nystagmus dystonia embryoma endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy focal hand dystonia fundus albipunctatus generalized dystonia giant cell glioblastoma glioblastoma hepatitis A hepatitis hepatocellular carcinoma high grade glioma hypertrichosis hypertrophic cardiomyopathy hypertropia inherited metabolic disorder lactic acidosis leukodystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma macrocytic anemia mal de Meleda mechanical strabismus mitochondrial metabolism disease narcolepsy nervous system disease neuropathy nonpapillary renal cell carcinoma obesity ophthalmoplegia optic atrophy overnutrition papillary renal cell carcinoma pathologic nystagmus peripheral nervous system disease periventricular leukomalacia ptosis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal carcinoma renal cell carcinoma restrictive dermopathy retinitis pigmentosa sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 ventricular septal defect visual epilepsy

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements