GlyCosmos Portal

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The O-GlcNAc Database	June 3, 2024
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Displaying entries **8701 - 8725** 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
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
Q3U2K5	Lysine-specific demethylase 4D	Kdm4d Jhdm3d Jmjd2d	Mus musculus (house mouse)	1	1
B7Z0L0	Fasciclin 1, isoform F	Fas1 DROFAS DROFAS1 DROFASI Dmel\CG6588 FGM222E05 Fas I FasI MRE24 fas I fas-I fas1 fasI gasI	Drosophila melanogaster (fruit fly)	0	1
A0A178UXN3	AT-hook motif nuclear-localized protein	AXX17_At4g26450	Arabidopsis thaliana (thale cress)	0	1
A0A494B955	Thioredoxin-like 1	Txnl1	Mus musculus (house mouse)	0	1
Q9CPR8	Non-structural maintenance of chromosomes element 3 homolog	Nsmce3 Mageg1 Ndnl2	Mus musculus (house mouse)	1	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
Q5YD48	APOBEC1 complementation factor	A1cf Acf Asp	Mus musculus (house mouse)	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
Q80V24	Transcription cofactor vestigial-like protein 4	Vgll4	Mus musculus (house mouse)	1	1
Q6NS60	F-box only protein 41	Fbxo41 D6Ertd538e Kiaa1940	Mus musculus (house mouse)	3	1
Q8R3E3	WD repeat domain phosphoinositide-interacting protein 1	Wipi1 D11Ertd498e	Mus musculus (house mouse)	1	1
Q96NG3	Outer dynein arm-docking complex subunit 4	ODAD4 TTC25	Homo sapiens (human)	0	1

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