GlyCosmos Portal

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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 **4626 - 4650** 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
A1L020	RNA-binding protein MEX3A	MEX3A RKHD4	Homo sapiens (human)	0	1
Q96JQ2	Calmin	CLMN KIAA1188	Homo sapiens (human)	0	1
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
Q6ZTI6	Refilin-A	RFLNA FAM101A	Homo sapiens (human)	1	1
P32314	Forkhead box protein N2	FOXN2 HTLF	Homo sapiens (human)	0	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
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
Q96G42	Kelch domain-containing protein 7B	KLHDC7B	Homo sapiens (human)	1	1
Q9H3R0	Lysine-specific demethylase 4C	KDM4C GASC1 JHDM3C JMJD2C KIAA0780	Homo sapiens (human)	1	1
Q9UBB4	Ataxin-10	ATXN10 SCA10	Homo sapiens (human)	0	1
P06703	Protein S100-A6	S100A6 CACY	Homo sapiens (human)	0	1
O00443	Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha	PIK3C2A	Homo sapiens (human)	7	1	Duchenne muscular dystrophy Gamstorp-Wohlfart syndrome Kaposi's sarcoma Laron syndrome Norum disease Tangier disease Unverricht-Lundborg syndrome abetalipoproteinemia achondroplasia acquired immunodeficiency syndrome acute myocardial infarction anodontia arteriosclerotic cardiovascular disease atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy blepharospasm breast cancer breast carcinoma cancer choreaacanthocytosis chronic monocytic leukemia congenital hypothyroidism congenital muscular dystrophy coronary artery disease coronary thrombosis cryptorchidism diabetes mellitus disease of mental health distal myopathy early myoclonic encephalopathy embryoma episodic ataxia type 1 facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia focal hand dystonia gastrointestinal stromal tumor glaucoma hypercalcemia hyperphosphatemia hypolipoproteinemia hypothyroidism leukopenia limb-girdle muscular dystrophy lymphoid leukemia muscular dystrophy myeloid leukemia myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis myotonic dystrophy type 2 myxedema nephrocalcinosis neuroleptic malignant syndrome nutmeg liver obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy phosphorus metabolism disease placental insufficiency protein-losing enteropathy psychotic disorder rippling muscle disease 2 schizoaffective disorder schizophrenia schizophreniform disorder scoliosis sensorineural hearing loss silent myocardial infarction systemic lupus erythematosus thrombocytopenia tibial muscular dystrophy tooth agenesis type 2 diabetes mellitus
Q58EX7	Puratrophin-1	PLEKHG4 PRTPHN1	Homo sapiens (human)	0	1
Q01970	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-3	PLCB3	Homo sapiens (human)	0	1	acrodermatitis acute myocardial infarction adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma cancer coronary thrombosis cribriform carcinoma cystic fibrosis dermatitis diabetes mellitus diabetic ketoacidosis essential hypertension extragonadal germ cell cancer granular cell carcinoma hyperparathyroidism hypertension lung cancer lung disease lung non-small cell carcinoma multiple endocrine neoplasia type 1 myocardial infarction neuroendocrine carcinoma neuroendocrine tumor osteitis fibrosa silent myocardial infarction tubular adenocarcinoma type 2 diabetes mellitus vitiligo
Q13643	Four and a half LIM domains protein 3	FHL3 SLIM2	Homo sapiens (human)	1	1
Q9Y2K1	Zinc finger and BTB domain-containing protein 1	ZBTB1 KIAA0997	Homo sapiens (human)	0	1
Q8WYQ5	Microprocessor complex subunit DGCR8	DGCR8 C22orf12 DGCRK6	Homo sapiens (human)	0	1
Q9NRP2	COX assembly mitochondrial protein 2 homolog	CMC2 C16orf61	Homo sapiens (human)	0	1
P61006	Ras-related protein Rab-8A	RAB8A MEL RAB8	Homo sapiens (human)	0	1
Q01581	Hydroxymethylglutaryl-CoA synthase, cytoplasmic	HMGCS1 HMGCS	Homo sapiens (human)	0	1	colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatitis C hepatoblastoma hepatocellular carcinoma large intestine cancer prostate cancer prostate carcinoma spinal cord disease
P36544	Neuronal acetylcholine receptor subunit alpha-7	CHRNA7 NACHRA7	Homo sapiens (human)	3	1
Q96NG3	Outer dynein arm-docking complex subunit 4	ODAD4 TTC25	Homo sapiens (human)	0	1
P23469	Receptor-type tyrosine-protein phosphatase epsilon	PTPRE	Homo sapiens (human)	2	1
P83881	Large ribosomal subunit protein eL42	RPL36A RPL44	Homo sapiens (human)	0	1

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