GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **107826 - 107850** 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
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
Q9UBB4	Ataxin-10	ATXN10 SCA10	Homo sapiens (human)	0	1
P06703	Protein S100-A6	S100A6 CACY	Homo sapiens (human)	0	1
P40850	Post-transcriptional regulator MKT1	MKT1	Saccharomyces cerevisiae S288C	9	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
P14426	H-2 class I histocompatibility antigen, D-K alpha chain	H2-D1	Mus musculus (house mouse)	3	1
Q8VCQ8	Caldesmon 1	Cald1	Mus musculus (house mouse)	0	1
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

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