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 **8676 - 8700** 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
Q9NX46	ADP-ribosylhydrolase ARH3	ADPRS ADPRHL2 ARH3	Homo sapiens (human)	0	1	autosomal recessive hypercholesterolemia brain stem infarction breast cancer breast carcinoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease congenital nystagmus congenital ptosis dissociated nystagmus epilepsy hypertropia intellectual disability learning disability mechanical strabismus neurodegenerative disease ophthalmoplegia pathologic nystagmus ptosis spontaneous ocular nystagmus strabismus visual epilepsy
A0A125YU34	Ribosomal protein RPL27 (Fragment)	TGVEG_262690	Toxoplasma gondii VEG	0	1
Q12427	Protein STB3	STB3	Saccharomyces cerevisiae S288C	20	1
Q6ZTI6	Refilin-A	RFLNA FAM101A	Homo sapiens (human)	1	1
A0A0A6YXH3	Oxysterol-binding protein	Osbpl9	Mus musculus (house mouse)	0	1
P32314	Forkhead box protein N2	FOXN2 HTLF	Homo sapiens (human)	0	1
Q924S8	Sprouty-related, EVH1 domain-containing protein 1	Spred1	Mus musculus (house mouse)	1	1
Q12873	Chromodomain-helicase-DNA-binding protein 3	CHD3	Homo sapiens (human)	1	1
P22415	Upstream stimulatory factor 1	USF1 BHLHB11 USF	Homo sapiens (human)	0	1
P62260	14-3-3 protein epsilon	Ywhae	Rattus norvegicus (Norway rat)	0	1
P40457	Protein MLP2	MLP2	Saccharomyces cerevisiae S288C	3	1
Q00519	Xanthine dehydrogenase/oxidase	Xdh	Mus musculus (house mouse)	0	1
P38606	V-type proton ATPase catalytic subunit A	ATP6V1A ATP6A1 ATP6V1A1 VPP2	Homo sapiens (human)	5	1	American histoplasmosis Dandy-Walker syndrome Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Unverricht-Lundborg syndrome achondroplasia agnosia angioma serpiginosum anodontia aspergillosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect attention deficit hyperactivity disorder autistic disorder autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID black piedra blepharophimosis blepharospasm brain disease capillary hemangioma cardiomyopathy cataract cavernous hemangioma cerebral degeneration clubfoot coccidioidomycosis coloboma colorectal cancer colorectal carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congenital ptosis congestive heart failure cortical dysplasia-focal epilepsy syndrome cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy endomyocardial fibrosis entropion epilepsy esophagitis familial hypertrophic cardiomyopathy focal hand dystonia gastroesophageal reflux disease histoplasmosis hydranencephaly hyperopia hypertrophic cardiomyopathy hypertropia inguinal hernia intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia lipoatrophic diabetes mellitus lipodystrophy lissencephaly mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy ophthalmoplegia optic atrophy patent foramen ovale pathologic nystagmus peptic esophagitis placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 ptosis retinal degeneration schizophrenia septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly spontaneous ocular nystagmus sporotrichosis status epilepticus stomach cancer stomach carcinoma strabismus superficial mycosis syndromic X-linked intellectual disability Najm type tooth agenesis visual epilepsy white piedra
D3Z4W3	AKT1 substrate 1 (proline-rich) (Fragment)	Akt1s1	Mus musculus (house mouse)	0	1
Q3UZA1	CapZ-interacting protein	Rcsd1 Capzip	Mus musculus (house mouse)	1	1
Q96G42	Kelch domain-containing protein 7B	KLHDC7B	Homo sapiens (human)	1	1
Q5SUH6	Clathrin interactor 1	Clint1	Mus musculus (house mouse)	0	1
Q9S3R9	Outer membrane protein 41	PG_0695	Porphyromonas gingivalis W83	0	1
Q5PRE5	Proline and serine-rich protein 1	Proser1	Mus musculus (house mouse)	7	1
V5D4R1	Choline/carnitine O-acyltransferase	TCDM_09869	Trypanosoma cruzi Dm28c	0	1
E9Q5C9	Nucleolar and coiled-body phosphoprotein 1	Nolc1 Kiaa0035	Mus musculus (house mouse)	0	1
Q9H3R0	Lysine-specific demethylase 4C	KDM4C GASC1 JHDM3C JMJD2C KIAA0780	Homo sapiens (human)	1	1
P45700	Mannosyl-oligosaccharide 1,2-alpha-mannosidase IA	Man1a1 Man1a	Mus musculus (house mouse)	1	1
Q99JH1	Ribonuclease P protein subunit p25-like protein	Rpp25l	Mus musculus (house mouse)	1	1
Q6PAJ1	Breakpoint cluster region protein	Bcr Kiaa3017	Mus musculus (house mouse)	2	1

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