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 **226 - 250** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q8NBN7	Retinol dehydrogenase 13	RDH13 SDR7C3	Homo sapiens (human)	1
P11802	Cyclin-dependent kinase 4	CDK4	Homo sapiens (human)	1
Q6P1Q9	tRNA N(3)-methylcytidine methyltransferase METTL2B	METTL2B	Homo sapiens (human)	1
Q9UKK9	ADP-sugar pyrophosphatase	NUDT5 NUDIX5	Homo sapiens (human)	1	breast cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
Q6ZV50	DNA-binding protein RFX8	RFX8	Homo sapiens (human)	1
O95249	Golgi SNAP receptor complex member 1	GOSR1 GS28	Homo sapiens (human)	1
P32019	Type II inositol 1,4,5-trisphosphate 5-phosphatase	INPP5B OCRL2	Homo sapiens (human)	1	Dent disease Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome amyotrophic lateral sclerosis 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 congenital hypothyroidism congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy giant cell glioblastoma glaucoma glioblastoma hypothyroidism limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myxedema 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 progressive muscular atrophy rippling muscle disease 2
Q8NG50	RAD52 motif-containing protein 1	RDM1 RAD52B	Homo sapiens (human)	1
Q9UHH9	Inositol hexakisphosphate kinase 2	IP6K2 IHPK2	Homo sapiens (human)	1
Q13404	Ubiquitin-conjugating enzyme E2 variant 1	UBE2V1 CROC1 UBE2V UEV1	Homo sapiens (human)	1
Q68E01	Integrator complex subunit 3	INTS3 C1orf193 C1orf60	Homo sapiens (human)	1
Q70EL3	Ubiquitin carboxyl-terminal hydrolase 50	USP50	Homo sapiens (human)	1
O00629	Importin subunit alpha-3	KPNA4 QIP1	Homo sapiens (human)	1
Q6GMV3	Putative peptidyl-tRNA hydrolase PTRHD1	PTRHD1 C2orf79	Homo sapiens (human)	1
Q14764	Major vault protein	MVP LRP	Homo sapiens (human)	1
P05062	Fructose-bisphosphate aldolase B	ALDOB ALDB	Homo sapiens (human)	1	Gilbert syndrome autoimmune hepatitis bilirubin metabolic disorder blood coagulation disease cancer cataract chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma diabetes mellitus diarrhea epilepsy hepatitis hepatocellular carcinoma hereditary fructose intolerance syndrome hyperglycemia hyperuricemia hypoglycemia hypophosphatemia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability kwashiorkor lactic acidosis large intestine cancer learning disability liver benign neoplasm liver cancer liver cirrhosis marasmus nonpapillary renal cell carcinoma nutrition disease obesity obsolete constipation obsolete inherited blood coagulation disease papillary renal cell carcinoma peritonitis protein-energy malnutrition rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal tubular acidosis sarcomatoid renal cell carcinoma steatotic liver disease stomach cancer stomach carcinoma type 2 diabetes mellitus ulcerative colitis visual epilepsy
Q9Y3C4	EKC/KEOPS complex subunit TPRKB	TPRKB	Homo sapiens (human)	1
Q9Y316	Protein MEMO1	MEMO1 C2orf4 MEMO NS5ATP7	Homo sapiens (human)	1
Q9NQ50	Large ribosomal subunit protein mL40	MRPL40 NLVCF URIM	Homo sapiens (human)	1
O14828	Secretory carrier-associated membrane protein 3	SCAMP3 C1orf3 PROPIN1	Homo sapiens (human)	1
Q9BV38	WD repeat-containing protein 18	WDR18	Homo sapiens (human)	1
P0CG32	Zinc finger CCHC domain-containing protein 18	ZCCHC18	Homo sapiens (human)	1
A8MPX8	Protein phosphatase 2C-like domain-containing protein 1	PP2D1 C3orf48	Homo sapiens (human)	1
P23434	Glycine cleavage system H protein, mitochondrial	GCSH	Homo sapiens (human)	1	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome blepharospasm brain disease breast cancer breast carcinoma cancer central nervous system lymphoma chondrodysplasia-pseudohermaphroditism syndrome early myoclonic encephalopathy embryoma epilepsy focal hand dystonia glycine encephalopathy intellectual disability learning disability lymphoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II obsolete ymphosarcoma schizophrenia urea cycle disorder visual epilepsy
P78314	SH3 domain-binding protein 2	SH3BP2 3BP2	Homo sapiens (human)	1

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