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 **19476 - 19500** of **126547** in total

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UniProt ID	Protein Name ▲	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q52LR7	Enhancer of polycomb homolog 2	EPC2	Homo sapiens (human)	3	1
Q8C0I4	Enhancer of polycomb homolog 2	Epc2	Mus musculus (house mouse)	1	1
P84089	Enhancer of rudimentary homolog	Erh	Mus musculus (house mouse)	0	1
P84090	Enhancer of rudimentary homolog	ERH	Homo sapiens (human)	0	1
G3UW85	Enhancer of rudimentary homolog	Erh	Mus musculus (house mouse)	0	1
E9QAU4	Enhancer trap locus 4	Etl4	Mus musculus (house mouse)	0	1
Q27727	Enolase	ENO	Plasmodium falciparum (malaria parasite P. falciparum)	0	1
Q7QDY3	Enolase-binding protein	EBP	Anopheles gambiae (African malaria mosquito)	4	0
Q9UHY7	Enolase-phosphatase E1	ENOPH1 MASA	Homo sapiens (human)	0	1
A0A077RX21	Enolase-phosphatase E1	CFC21_039897	Triticum aestivum (bread wheat)	0	1
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
P42125	Enoyl-CoA delta isomerase 1, mitochondrial	Eci1 Dci	Mus musculus (house mouse)	0	1
Q5XIC0	Enoyl-CoA delta isomerase 2	Eci2 Peci	Rattus norvegicus (Norway rat)	1	1
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
Q9WUR2	Enoyl-CoA delta isomerase 2	Eci2 Peci	Mus musculus (house mouse)	0	1
V5DTT7	Enoyl-CoA hydratase	TCDM_00259	Trypanosoma cruzi Dm28c	0	1
Q9D7J9	Enoyl-CoA hydratase domain-containing protein 3, mitochondrial	Echdc3	Mus musculus (house mouse)	0	1
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
P14604	Enoyl-CoA hydratase, mitochondrial	Echs1	Rattus norvegicus (Norway rat)	3	1
Q8BH95	Enoyl-CoA hydratase, mitochondrial	Echs1	Mus musculus (house mouse)	0	1
V5BN63	Enoyl-CoA hydratase/Enoyl-CoA isomerase/3-hydroxyacyl-CoA dehydrogenase	TCDM_05446	Trypanosoma cruzi Dm28c	0	1
Q4CWM5	Enoyl-CoA hydratase/isomerase family protein, putative	Tc00.1047053510997.40	Trypanosoma cruzi strain CL Brener	0	1
E9PUY9	Enoyl-Coenzyme A delta isomerase 2 (Fragment)	Eci2	Mus musculus (house mouse)	0	1
V5DBG0	Enoyl-[acyl-carrier-protein] reductase, mitochondrial	TCDM_14312	Trypanosoma cruzi Dm28c	0	1
Q9DCS3	Enoyl-[acyl-carrier-protein] reductase, mitochondrial	Mecr Nrbf1	Mus musculus (house mouse)	0	1

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