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 **13151 - 13175** 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
Q9SSA7	GDSL esterase/lipase 5	GLIP5	Arabidopsis thaliana (thale cress)	5	0
P28081	Hemagglutinin glycoprotein	H	Measles virus strain Yamagata-1	5	0
Q920V1	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1	B3galnt1 B3galt3 B3gt3 Mbrn1	Mus musculus (house mouse)	5	3
Q2TLY1	Macoilin-2	maco1b tmem57b	Danio rerio (zebrafish)	5	0
Q92794	Histone acetyltransferase KAT6A	KAT6A MOZ MYST3 RUNXBP2 ZNF220	Homo sapiens (human)	5	1
Q3UHD9	Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2	Agap2 Centg1 Kiaa0167	Mus musculus (house mouse)	5	1
O74189	Dolichyl-phosphate-mannose--protein mannosyltransferase 1	PMT1	Candida albicans SC5314	5	0
Q5XHM7	Carbohydrate sulfotransferase 12	chst12	Xenopus laevis (African clawed frog)	5	0
Q68FV6	Glycosylated lysosomal membrane protein	Glmp	Rattus norvegicus (Norway rat)	5	0
P33618	Kappa-casein	CSN3 CSN10 CSNK	Oryctolagus cuniculus (rabbit)	5	0
Q8NBL1	Protein O-glucosyltransferase 1	POGLUT1 C3orf9 CLP46 KTELC1 MDSRP	Homo sapiens (human)	5	23	Dowling-Degos disease Duchenne muscular dystrophy T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia acute myeloid leukemia 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 cancer childhood T-cell acute lymphoblastic leukemia childhood leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy embryoma essential thrombocythemia facioscapulohumeral muscular dystrophy hematopoietic system disease isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leukemia limb-girdle muscular dystrophy lung cancer lung non-small cell carcinoma mongolian spot muscular dystrophy myelodysplastic syndrome myofibrillar myopathy 1 myofibrillar myopathy 3 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 primary biliary cholangitis pseudoxanthoma elasticum reticulate acropigmentation of Kitamura rippling muscle disease 2
P42073	RNA end formation protein 2	REF2	Saccharomyces cerevisiae S288C	5	1
Q60587	Trifunctional enzyme subunit beta, mitochondrial	Hadhb	Rattus norvegicus (Norway rat)	5	1
P51659	Peroxisomal multifunctional enzyme type 2	HSD17B4 EDH17B4 SDR8C1	Homo sapiens (human)	5	2	Addison's disease Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Clouston syndrome D-bifunctional protein deficiency Friedreich ataxia Laron syndrome Perrault syndrome Pick's disease Refsum disease Reye syndrome Turner syndrome West syndrome Zellweger syndrome achondroplasia adrenal carcinoma adrenal cortex cancer adrenal cortical hypofunction adrenocortical carcinoma adrenoleukodystrophy alpha-methylacyl-CoA racemase deficiency androgen insensitivity syndrome beta-ketothiolase deficiency blindness breast cancer breast carcinoma cancer carnitine palmitoyltransferase I deficiency cerebellar ataxia cerebellar disease cerebral degeneration cholestasis clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital bile acid synthesis defect 4 congenital nystagmus craniosynostosis cystic kidney disease diabetic ketoacidosis dissociated nystagmus endometrial cancer endometrial carcinoma epilepsy essential hypertension gonadal dysgenesis hepatocellular carcinoma hereditary ataxia hydrocephalus hypertension hypertropia infantile Refsum disease large intestine cancer leukodystrophy liver cancer liver carcinoma mechanical strabismus non-congenital cyst of kidney obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 ophthalmoplegia osteoporosis pathologic nystagmus peroxisomal disease peroxisome biogenesis disorder 1A polycystic ovary syndrome polyhydramnios premature menopause primary cerebellar degeneration primary ovarian insufficiency prostate cancer prostate carcinoma rhizomelic chondrodysplasia punctata type 1 scoliosis seminoma sensorineural hearing loss spontaneous ocular nystagmus steatotic liver disease strabismus testicular cancer testicular germ cell cancer type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus uterine corpus cancer visual epilepsy
Q9T042	Protein disulfide-isomerase 5-4	PDIL5-4 PDI7 PDIL8-2	Arabidopsis thaliana (thale cress)	5	0
Q6P734	Plasma protease C1 inhibitor	Serping1	Rattus norvegicus (Norway rat)	5	0
B9W4V6	Aromatic peroxygenase	APO1	Cyclocybe aegerita	5	0
B5BQV4	Neurotrophic tyrosine kinase receptor, type2, splicing variant T3 beta	Ntrk2 ntrk2	Mus musculus (house mouse)	5	0
Q8VYG0	LEAF RUST 10 DISEASE-RESISTANCE LOCUS RECEPTOR-LIKE PROTEIN KINASE-like 1.3	LRK10L-1.3 LRK10L3	Arabidopsis thaliana (thale cress)	5	0
Q86IW5	Transmembrane protein DDB_G0274347	DDB_G0274347	Dictyostelium discoideum	5	0
B0YDW9	Probable feruloyl esterase B-1	faeB-1	Aspergillus fumigatus A1163	5	0
A0A179H0I7	Cytochrome P450 monooxygenase lcsI	lcsI	Purpureocillium lilacinum	5	0
O62728	Leukemia inhibitory factor	LIF	Neogale vison (American mink)	5	0
A0A072VG05	GDSL esterase/lipase ENOD8	ENOD8 Enod8.1	Medicago truncatula (barrel medic)	5	0
Q5VYJ5	MAM and LDL-receptor class A domain-containing protein 1	MALRD1 C10orf112 DIET1	Homo sapiens (human)	5	2

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