GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **11501 - 11525** 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
Q97ML2	Predicted acetyltransferase	CA_C0184	Clostridium acetobutylicum ATCC 824	5	0
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
Q60NC0	Degenerin mec-10	mec-10	Caenorhabditis briggsae	5	0
Q3TR36	P2X purinoceptor	P2rx4	Mus musculus (house mouse)	5	0
Q9H7M9	V-type immunoglobulin domain-containing suppressor of T-cell activation	VSIR C10orf54 SISP1 VISTA	Homo sapiens (human)	5	15
Q9C0B0	RING finger protein unkempt homolog	UNK KIAA1753 ZC3H5 ZC3HDC5	Homo sapiens (human)	5	2
Q9FH86	Receptor-like protein 57	RLP57	Arabidopsis thaliana (thale cress)	5	0
Q60849	CD98 heavy chain	Slc3a2	Mus musculus (house mouse)	5	0
Q15032	R3H domain-containing protein 1	R3HDM1 KIAA0029 R3HDM	Homo sapiens (human)	5	2
O95388	CCN family member 4	CCN4 WISP1	Homo sapiens (human)	5	1
Q5RAL8	OX-2 membrane glycoprotein	CD200	Pongo abelii (Sumatran orangutan)	5	0
P09343	Hemagglutinin	HA	Influenza A virus (A/chicken/Victoria/1985(H7N7))	5	0
P21463	Thyrotropin receptor	Tshr	Rattus norvegicus (Norway rat)	5	0
P97607	Protein jagged-2 (Fragment)	Jag2	Rattus norvegicus (Norway rat)	5	0
P79953	Ovochymase-2	ovch2 ovtn	Xenopus laevis (African clawed frog)	5	0
P49290	Eosinophil peroxidase	Epx Eper	Mus musculus (house mouse)	5	0
P48029	Sodium- and chloride-dependent creatine transporter 1	SLC6A8	Homo sapiens (human)	5	3
Q8NCW0	Kremen protein 2	KREMEN2 KRM2	Homo sapiens (human)	5	1
Q949U4	O-fucosyltransferase 16	OFUT16	Arabidopsis thaliana (thale cress)	5	0
Q9IH63	Fusion glycoprotein F0	F	Henipavirus nipahense	5	0
Q9ZUV3	Probable glucuronoxylan glucuronosyltransferase IRX7	IRX7 FRA8	Arabidopsis thaliana (thale cress)	5	0
Q6DBU8	Lipase member H	liph	Danio rerio (zebrafish)	5	0
P70031	Cholecystokinin receptor	cckar	Xenopus laevis (African clawed frog)	5	0
O08602	Retinoic acid early-inducible protein 1-alpha	Raet1a	Mus musculus (house mouse)	5	0
Q63691	Monocyte differentiation antigen CD14	Cd14	Rattus norvegicus (Norway rat)	5	0

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