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 **3726 - 3750** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▲	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8IZ81	ELMO domain-containing protein 2	ELMOD2	Homo sapiens (human)	3	1
Q96FG2	ELMO domain-containing protein 3	ELMOD3 RBED1 RBM29	Homo sapiens (human)	0	1
P15502	Elastin	ELN	Homo sapiens (human)	2	1
Q14241	Elongin-A	ELOA TCEB3	Homo sapiens (human)	1	1
Q8IYF1	Elongin-A2	ELOA2 TCEB3B TCEB3L	Homo sapiens (human)	3	2
Q15370	Elongin-B	ELOB TCEB2	Homo sapiens (human)	0	1
Q15369	Elongin-C	ELOC TCEB1	Homo sapiens (human)	0	1
Q9BW60	Very long chain fatty acid elongase 1	ELOVL1 SSC1	Homo sapiens (human)	0	1	Cauda equina syndrome acanthosis nigricans acrodermatitis adrenoleukodystrophy cancer dermatitis dry eye syndrome hyperglycemia neurogenic bladder obsolete asthenopia xerophthalmia
Q9HB03	Very long chain fatty acid elongase 3	ELOVL3 CIG30	Homo sapiens (human)	2	0	amnestic disorder atopic dermatitis dermatitis diabetes mellitus diabetic ketoacidosis ichthyosis prostate cancer prostate carcinoma retrograde amnesia type 2 diabetes mellitus
Q9GZR5	Very long chain fatty acid elongase 4	ELOVL4	Homo sapiens (human)	2	6	Kuhnt-Junius degeneration Leber congenital amaurosis Sjogren-Larsson syndrome Stargardt disease achromatopsia acquired color blindness acquired hyperkeratosis acute myocardial infarction age related macular degeneration alternating hemiplegia of childhood angioedema anhidrosis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis blindness blue color blindness cancer cardiac arrest central nervous system disease cerebellar ataxia cerebellar disease color blindness cone-rod dystrophy 2 cone-rod dystrophy 7 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis dissociated nystagmus dry eye syndrome epilepsy erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis eye disease fundus albipunctatus glycogen storage disease II granuloma annulare hepatocellular carcinoma hypertropia hypohidrosis ichthyosis inguinal hernia keratosis follicularis liver cancer locked-in syndrome macular degeneration mechanical strabismus mongolian spot myocardial infarction nervous system disease neurodegenerative disease night blindness obsolete congenital ichthyosiform erythroderma ophthalmoplegia pathologic nystagmus pseudoxanthoma elasticum quadriplegia red color blindness red-green color blindness retinitis pigmentosa 25 retinitis pigmentosa 30 retinitis pigmentosa silent myocardial infarction skin disease spinocerebellar ataxia type 34 spontaneous ocular nystagmus strabismus thrombocytopenia type 2 diabetes mellitus urticaria visual epilepsy xerophthalmia
Q9NYP7	Very long chain fatty acid elongase 5	ELOVL5 ELOVL2	Homo sapiens (human)	0	1	acute myocardial infarction autosomal dominant cerebellar ataxia cancer cardiac arrest cerebellar ataxia cerebellar disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus embryoma glaucoma glomerulonephritis hyperglycemia kidney disease large intestine cancer low tension glaucoma major depressive disorder melancholic depression myocardial infarction nephritis nephrosis obesity obsolete melancholia pathologic nystagmus primary open angle glaucoma prostate cancer prostate carcinoma pyoureter retinitis pigmentosa 25 schizophrenia silent myocardial infarction spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spinocerebellar ataxia type 38 spinocerebellar ataxia type 5 spinocerebellar ataxia type 6 spinocerebellar ataxia type 7 spontaneous ocular nystagmus steatotic liver disease type 2 diabetes mellitus
Q9H5J4	Very long chain fatty acid elongase 6	ELOVL6 FACE LCE	Homo sapiens (human)	2	2	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
O95163	Elongator complex protein 1	ELP1 IKAP IKBKAP	Homo sapiens (human)	0	1
Q6IA86	Elongator complex protein 2	ELP2 STATIP1	Homo sapiens (human)	1	2
Q9H9T3	Elongator complex protein 3	ELP3	Homo sapiens (human)	0	1
Q96EB1	Elongator complex protein 4	ELP4 C11orf19 PAXNEB	Homo sapiens (human)	3	2
Q96BH3	Epididymal sperm-binding protein 1	ELSPBP1 E12	Homo sapiens (human)	1	0
Q6PCB8	Embigin	EMB	Homo sapiens (human)	9	3
Q8N766	ER membrane protein complex subunit 1	EMC1 KIAA0090	Homo sapiens (human)	3	15
Q5UCC4	ER membrane protein complex subunit 10	EMC10 C19orf63 INM02	Homo sapiens (human)	4	8
Q15006	ER membrane protein complex subunit 2	EMC2 KIAA0103 TTC35	Homo sapiens (human)	1	1
Q9NPA0	Endoplasmic reticulum membrane protein complex subunit 7	EMC7 C11orf3 C15orf24	Homo sapiens (human)	3	2
O43402	ER membrane protein complex subunit 8	EMC8 C16orf2 C16orf4 COX4AL COX4NB FAM158B NOC4	Homo sapiens (human)	2	1
Q9ULC0	Endomucin	EMCN EMCN2 MUC14	Homo sapiens (human)	17	7
P50402	Emerin	EMD EDMD STA	Homo sapiens (human)	12	3

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