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 **18101 - 18125** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
P07949	Proto-oncogene tyrosine-protein kinase receptor Ret	RET CDHF12 CDHR16 PTC	Homo sapiens (human)	16	4
Q86VZ4	Low-density lipoprotein receptor-related protein 11	LRP11	Homo sapiens (human)	16	7
Q6EMK4	Vasorin	VASN SLITL2	Homo sapiens (human)	17	55
Q13443	Disintegrin and metalloproteinase domain-containing protein 9	ADAM9 KIAA0021 MCMP MDC9 MLTNG	Homo sapiens (human)	17	26
P19823	Inter-alpha-trypsin inhibitor heavy chain H2	ITIH2 IGHEP2	Homo sapiens (human)	17	62
P08648	Integrin alpha-5	ITGA5 FNRA	Homo sapiens (human)	17	115
O15072	A disintegrin and metalloproteinase with thrombospondin motifs 3	ADAMTS3 KIAA0366	Homo sapiens (human)	17	5
P54289	Voltage-dependent calcium channel subunit alpha-2/delta-1	CACNA2D1 CACNL2A CCHL2A MHS3	Homo sapiens (human)	17	53	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome West syndrome Williams-Beuren syndrome acute myeloid leukemia amelogenesis imperfecta type 1G atrial fibrillation atrioventricular block azoospermia cancer cardiac arrest colon cancer colonic benign neoplasm colorectal cancer depressive disorder embryoma epilepsy essential hypertension glaucoma hepatocellular carcinoma hypertension idiopathic scoliosis intellectual disability large intestine cancer learning disability liver cancer major depressive disorder malignant hyperthermia melancholic depression neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia primary open angle glaucoma short QT syndrome sick sinus syndrome stomach cancer stomach carcinoma supravalvular aortic stenosis uveal melanoma
O75339	Cartilage intermediate layer protein 1	CILP	Homo sapiens (human)	17	19
O43432	Eukaryotic translation initiation factor 4 gamma 3	EIF4G3	Homo sapiens (human)	17	3
Q9H8L6	Multimerin-2	MMRN2 EMILIN3	Homo sapiens (human)	17	89
Q04721	Neurogenic locus notch homolog protein 2	NOTCH2	Homo sapiens (human)	17	9
Q9NZV1	Cysteine-rich motor neuron 1 protein	CRIM1 S52	Homo sapiens (human)	17	5
Q99700	Ataxin-2	ATXN2 ATX2 SCA2 TNRC13	Homo sapiens (human)	17	1
A6NF01	Putative nuclear envelope pore membrane protein POM 121B	POM121B	Homo sapiens (human)	17	1
O95490	Adhesion G protein-coupled receptor L2	ADGRL2 KIAA0786 LEC1 LPHH1 LPHN2	Homo sapiens (human)	17	13
P00747	Plasminogen	PLG	Homo sapiens (human)	17	65
Q96DR8	Mucin-like protein 1	MUCL1 SBEM	Homo sapiens (human)	17	1
P78527	DNA-dependent protein kinase catalytic subunit	PRKDC HYRC HYRC1	Homo sapiens (human)	17	7
Q9H4F8	SPARC-related modular calcium-binding protein 1	SMOC1	Homo sapiens (human)	17	9
Q9UKM7	Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase	MAN1B1	Homo sapiens (human)	17	4	Hailey-Hailey disease Rafiq syndrome Rothmund-Thomson syndrome agnosia alpha 1-antitrypsin deficiency autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bladder carcinoma bulimia nervosa cancer cerebral degeneration choreatic disease congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation cutis laxa depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease hepatocellular carcinoma hyperopia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver disease major depressive disorder mal de Meleda melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia oophoritis parametritis partial motor epilepsy pelvic inflammatory disease periventricular nodular heterotopia pyosalpinx restrictive dermopathy salpingitis stereotypic movement disorder syndactyly syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 urinary bladder cancer visual epilepsy
O14786	Neuropilin-1	NRP1 NRP VEGF165R	Homo sapiens (human)	17	58
Q9NTZ6	RNA-binding protein 12	RBM12 KIAA0765	Homo sapiens (human)	17	3
Q9H1B7	Probable E3 ubiquitin-protein ligase IRF2BPL	IRF2BPL C14orf4 EAP1 KIAA1865	Homo sapiens (human)	17	3
Q5T8P6	RNA-binding protein 26	RBM26 C13orf10	Homo sapiens (human)	17	5

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