GlyCosmos Portal

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UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9H2F5	Enhancer of polycomb homolog 1	EPC1	6	1
Q52LR7	Enhancer of polycomb homolog 2	EPC2	3	1
P84090	Enhancer of rudimentary homolog	ERH	0	1
Q9UHY7	Enolase-phosphatase E1	ENOPH1 MASA	0	1
P42126	Enoyl-CoA delta isomerase 1, mitochondrial	ECI1 DCI	0	1	achalasia carcinoma congenital diaphragmatic hernia dilated cardiomyopathy 1A dilated cardiomyopathy esophagitis gastroesophageal reflux disease hiatus hernia megaesophagus peptic esophagitis
O75521	Enoyl-CoA delta isomerase 2	ECI2 DRS1 HCA88 PECI	0	1	aplastic anemia paroxysmal nocturnal hemoglobinuria prostate cancer prostate carcinoma pure red-cell aplasia
P30084	Enoyl-CoA hydratase, mitochondrial	ECHS1	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
Q14244	Ensconsin	MAP7	5	2
P98073	Enteropeptidase	TMPRSS15 ENTK PRSS7	18	1
Q92817	Envoplakin	EVPL	2	1
P12724	Eosinophil cationic protein	RNASE3 ECP RNS3	3	0
P11678	Eosinophil peroxidase	EPX EPER EPO EPP	6	4
P51671	Eotaxin	CCL11 SCYA11	1	1
P21709	Ephrin type-A receptor 1	EPHA1 EPH EPHT EPHT1	1	0
Q5JZY3	Ephrin type-A receptor 10	EPHA10	2	0
P29317	Ephrin type-A receptor 2	EPHA2 ECK	3	8
P29320	Ephrin type-A receptor 3	EPHA3 ETK ETK1 HEK TYRO4	5	0
P54764	Ephrin type-A receptor 4	EPHA4 HEK8 SEK TYRO1	4	2
P54756	Ephrin type-A receptor 5	EPHA5 BSK EHK1 HEK7 TYRO4	8	3
Q9UF33	Ephrin type-A receptor 6	EPHA6 EHK2 HEK12	3	0
Q15375	Ephrin type-A receptor 7	EPHA7 EHK3 HEK11	5	2
P29322	Ephrin type-A receptor 8	EPHA8 EEK HEK3 KIAA1459	4	1
P54762	Ephrin type-B receptor 1	EPHB1 ELK EPHT2 HEK6 NET	4	1
P29323	Ephrin type-B receptor 2	EPHB2 DRT EPHT3 EPTH3 ERK HEK5 TYRO5	5	3
E2I6F7	Ephrin type-B receptor 2 variant (Fragment)	EPHB2	1	0

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