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 **3151 - 3175** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
P10916	Myosin regulatory light chain 2, ventricular/cardiac muscle isoform	MYL2 MLC2	Homo sapiens (human)	1
Q8WW18	Uncharacterized protein C17orf50	C17orf50	Homo sapiens (human)	1
Q9H8G1	Zinc finger protein 430	ZNF430	Homo sapiens (human)	1
Q9GZN2	Homeobox protein TGIF2	TGIF2	Homo sapiens (human)	1
Q9BPW8	Protein NipSnap homolog 1	NIPSNAP1	Homo sapiens (human)	1
A6NCL7	Ankyrin repeat domain-containing protein 33B	ANKRD33B	Homo sapiens (human)	1
O43765	Small glutamine-rich tetratricopeptide repeat-containing protein alpha	SGTA SGT SGT1	Homo sapiens (human)	1
Q14192	Four and a half LIM domains protein 2	FHL2 DRAL SLIM3	Homo sapiens (human)	1
O43809	Cleavage and polyadenylation specificity factor subunit 5	NUDT21 CFIM25 CPSF25 CPSF5	Homo sapiens (human)	1
Q96SU4	Oxysterol-binding protein-related protein 9	OSBPL9 ORP9 OSBP4	Homo sapiens (human)	1
Q15424	Scaffold attachment factor B1	SAFB HAP HET SAFB1	Homo sapiens (human)	1
Q02535	DNA-binding protein inhibitor ID-3	ID3 1R21 BHLHB25 HEIR1	Homo sapiens (human)	1
P00352	Aldehyde dehydrogenase 1A1	ALDH1A1 ALDC ALDH1 PUMB1	Homo sapiens (human)	1
Q92544	Transmembrane 9 superfamily member 4	TM9SF4 KIAA0255 TUCAP1	Homo sapiens (human)	1
Q9HCL2	Glycerol-3-phosphate acyltransferase 1, mitochondrial	GPAM GPAT1 KIAA1560	Homo sapiens (human)	1	cancer embryoma familial nephrotic syndrome lipoid nephrosis melanoma nephrotic syndrome obesity overnutrition skin melanoma steatotic liver disease
Q86UN6	A-kinase anchor protein 14	AKAP14 AKAP28	Homo sapiens (human)	1
Q9H0U4	Ras-related protein Rab-1B	RAB1B	Homo sapiens (human)	1
P62861	Ubiquitin-like FUBI-ribosomal protein eS30 fusion protein	FAU	Homo sapiens (human)	1
Q9NQC7	Ubiquitin carboxyl-terminal hydrolase CYLD	CYLD CYLD1 KIAA0849	Homo sapiens (human)	1
P23786	Carnitine O-palmitoyltransferase 2, mitochondrial	CPT2 CPT1	Homo sapiens (human)	1	Chanarin-Dorfman syndrome Meckel syndrome Pearson syndrome Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis attention deficit hyperactivity disorder autosomal dominant polycystic kidney disease beta thalassemia brain disease brain edema breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency carnitine palmitoyltransferase II deficiency cataract chronic fatigue syndrome chronic kidney disease clubfoot colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy essential thrombocythemia familial hyperlipidemia familial periodic paralysis fibromyalgia glycogen storage disease II glycogen storage disease V hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hydronephrosis hyperglycemia hypertrophic cardiomyopathy hypoglycemia influenza isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer liver cancer liver cirrhosis medium chain acyl-CoA dehydrogenase deficiency microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency myelitis myelodysplastic syndrome myocardial infarction myoglobinuria myopathy myositis neurogenic arthropathy neuroleptic malignant syndrome obesity ovarian cancer pancytopenia placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma pseudosarcomatous fibromatosis psoriatic arthritis sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction status epilepticus steatotic liver disease systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency viral infectious disease visual epilepsy
O75923	Dysferlin	DYSF FER1L1	Homo sapiens (human)	1
Q7Z4W1	L-xylulose reductase	DCXR SDR20C1	Homo sapiens (human)	1	arthritis arthropathy cancer carcinoma hemophilia B hepatocellular carcinoma liver cancer pentosuria prostate adenocarcinoma prostate cancer prostate carcinoma renal glycosuria sarcomatoid carcinoma
O43818	U3 small nucleolar RNA-interacting protein 2	RRP9 RNU3IP2 U355K	Homo sapiens (human)	1
Q8NB90	ATPase family gene 2 protein homolog A	AFG2A SPAF SPATA5	Homo sapiens (human)	1
Q9Y3C1	Nucleolar protein 16	NOP16	Homo sapiens (human)	1

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