GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q8NGJ2	Olfactory receptor 52H1	OR52H1	2	0
P51956	Serine/threonine-protein kinase Nek3	NEK3	2	1
Q08289	Voltage-dependent L-type calcium channel subunit beta-2	CACNB2 CACNLB2 MYSB	2	1
Q6UXT8	ALK and LTK ligand 1	ALKAL1 FAM150A	2	1
Q9NQZ7	Ectonucleoside triphosphate diphosphohydrolase 7	ENTPD7 LALP1	2	2
A0A7I2V5B9	Cathepsin F	CTSF	2	0
H0YNK6	Tyrosine-protein kinase receptor TYRO3	TYRO3	2	0
P49419	Alpha-aminoadipic semialdehyde dehydrogenase	ALDH7A1 ATQ1	2	1	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 Balo concentric sclerosis Becker muscular dystrophy Dravet syndrome Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pendred Syndrome Pick's disease Reye syndrome Richter's syndrome Usher syndrome type 1 Usher syndrome acrodermatitis adrenoleukodystrophy adult respiratory distress syndrome allergic asthma asphyxia neonatorum asthma atopic dermatitis 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 bone disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cartilage disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholera chronic lymphocytic leukemia coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy congestive heart failure connective tissue disease depressive disorder dermatitis developmental and epileptic encephalopathy 2 diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health distal myopathy dyshormonogenic goiter dysthymic disorder early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential hypertension facioscapulohumeral muscular dystrophy fundus albipunctatus gastrointestinal stromal tumor giant cell glioblastoma glaucoma glioblastoma heart disease hepatitis C hepatocellular carcinoma high grade glioma homocystinuria hydrocephalus hyperprolinemia type 2 hypertension hypertropia hypophosphatasia impotence intellectual disability intermittent claudication intrinsic asthma keratosis follicularis lactic acidosis large intestine cancer learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma major depressive disorder mechanical strabismus melancholic depression melanoma microphthalmia mongolian spot movement disease muscular dystrophy narcolepsy nervous system disease neurotic disorder newborn respiratory distress syndrome nodular prostate obsolete Dravet syndrome obsolete Matthew-Wood syndrome 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 obsolete infantile epileptic encephalopathy obsolete melancholia oculopharyngeal muscular dystrophy open-angle glaucoma ophthalmoplegia osteoporosis peripheral artery disease peripheral vascular disease pigment dispersion syndrome pneumonia premature ejaculation primary pulmonary hypertension prostate cancer prostate carcinoma prostatic adenoma pseudoxanthoma elasticum psychologic dyspareunia psychotic disorder rectal benign neoplasm rectum adenocarcinoma rectum cancer retinitis pigmentosa sarcomatoid carcinoma schizophrenia seminoma sexual dysfunction skin melanoma speech disorder squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma strabismus testicular cancer testicular germ cell cancer tongue squamous cell carcinoma type 2 diabetes mellitus visual epilepsy
P13797	Plastin-3	PLS3	2	2
P04234	T-cell surface glycoprotein CD3 delta chain	CD3D T3D	2	0
Q9Y5X4	Photoreceptor-specific nuclear receptor	NR2E3 PNR RNR	2	1
Q8TAS6	LAMB1 protein (Fragment)	LAMB1	2	0
O43324	Eukaryotic translation elongation factor 1 epsilon-1	EEF1E1 AIMP3 P18	2	1
Q6UUV9	CREB-regulated transcription coactivator 1	CRTC1 KIAA0616 MECT1 TORC1 WAMTP1	2	2
Q53H76	Phospholipase A1 member A	PLA1A NMD PSPLA1	2	1
Q86SU0	Immunoglobulin-like domain-containing receptor 1	ILDR1	2	1
Q8NC96	Adaptin ear-binding coat-associated protein 1	NECAP1	2	2
Q8NGJ3	Olfactory receptor 52E1	OR52E1 OR52E1P	2	1
Q7L2H7	Eukaryotic translation initiation factor 3 subunit M	EIF3M HFLB5 PCID1	2	1
Q9UKR3	Kallikrein-13	KLK13 KLKL4	2	0
Q9NPB9	Atypical chemokine receptor 4	ACKR4 CCBP2 CCR11 CCRL1 VSHK1	2	0
Q86UU1	Pleckstrin homology-like domain family B member 1	PHLDB1 KIAA0638 LL5A	2	2
A0A3B3ISA6	Complement C4B (Chido blood group) (Fragment)	C4B	2	0
A0A7P0Z415	Cathepsin V	CTSV	2	0
O75165	DnaJ homolog subfamily C member 13	DNAJC13 KIAA0678 RME8	2	2

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