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 **14751 - 14775** 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
Q96AE7	Tetratricopeptide repeat protein 17	TTC17	Homo sapiens (human)	7	13
Q96AG4	Leucine-rich repeat-containing protein 59	LRRC59	Homo sapiens (human)	0	1
Q96AH0	SOSS complex subunit B2	NABP1 OBFC2A SSB2	Homo sapiens (human)	1	1
Q96AM1	Mas-related G-protein coupled receptor member F	MRGPRF GPR140 GPR168 MRGF	Homo sapiens (human)	1	0
Q96AP4	Zinc finger-containing ubiquitin peptidase 1	ZUP1 C6orf113 ZUFSP	Homo sapiens (human)	0	1
Q96AP7	Endothelial cell-selective adhesion molecule	ESAM	Homo sapiens (human)	5	28
Q96AQ1	Coiled-coil domain-containing protein 74A	CCDC74A	Homo sapiens (human)	1	1
Q96AQ6	Pre-B-cell leukemia transcription factor-interacting protein 1	PBXIP1 HPIP	Homo sapiens (human)	2	14
Q96AR9	PLOD2 protein (Fragment)	PLOD2	Homo sapiens (human)	1	0
Q96AT9	Ribulose-phosphate 3-epimerase	RPE	Homo sapiens (human)	1	1	CINCA Syndrome Doyne honeycomb retinal dystrophy Leber congenital amaurosis 1 Leber congenital amaurosis 2 Sorsby's fundus dystrophy Stargardt disease Sveinsson chorioretinal atrophy Usher syndrome type 1 Vogt-Koyanagi-Harada disease Zika fever age related macular degeneration atrial fibrillation basal laminar drusen blindness cancer cardiovascular system disease choroideremia chronic recurrent multifocal osteomyelitis ciliary body disease colon cancer colonic benign neoplasm colorectal cancer cone-rod dystrophy degeneration of macula and posterior pole diabetes mellitus diabetic cataract diabetic macular edema diabetic retinopathy embryoma eye disease familial adenomatous polyposis 1 familial adenomatous polyposis familial retinoblastoma fundus albipunctatus fundus dystrophy glycogen storage disease II heart disease hepatocellular carcinoma hole retinal cyst hyperopia iris disease islet cell tumor large intestine cancer liver cancer liver carcinoma locked-in syndrome macular degeneration macular holes melanoma myopia neovascular inflammatory vitreoretinopathy neurodegenerative disease panuveitis peripheral retinal degeneration phototoxic dermatitis preretinal fibrosis proliferative diabetic retinopathy quadriplegia retinal detachment retinal disease retinal lattice degeneration retinal perforation retinitis pigmentosa 30 retinitis pigmentosa retinitis retinoblastoma retinoschisis skin melanoma trilateral retinoblastoma type 2 diabetes mellitus uveitis vitelliform macular dystrophy
Q96AV8	Transcription factor E2F7	E2F7	Homo sapiens (human)	1	1
Q96AY3	Peptidyl-prolyl cis-trans isomerase FKBP10	FKBP10 FKBP65	Homo sapiens (human)	12	53
Q96AY4	Tetratricopeptide repeat protein 28	TTC28 KIAA1043 TPRBK	Homo sapiens (human)	5	1
Q96B01	RAD51-associated protein 1	RAD51AP1 PIR51	Homo sapiens (human)	1	2
Q96B18	Dapper homolog 3	DACT3 RRR1	Homo sapiens (human)	2	1
Q96B23	Protein ARK2N	ARK2N ARKL1 C18orf25	Homo sapiens (human)	2	1
Q96B26	Exosome complex component RRP43	EXOSC8 OIP2 RRP43	Homo sapiens (human)	1	2
Q96B36	Proline-rich AKT1 substrate 1	AKT1S1 PRAS40	Homo sapiens (human)	3	2
Q96B45	BLOC-1-related complex subunit 7	BORCS7 C10orf32	Homo sapiens (human)	0	1
Q96B49	Mitochondrial import receptor subunit TOM6 homolog	TOMM6 OBTP TOM6	Homo sapiens (human)	4	2
Q96B70	Leukocyte receptor cluster member 9	LENG9	Homo sapiens (human)	0	1
Q96B86	Repulsive guidance molecule A	RGMA RGM	Homo sapiens (human)	4	3	Mycobacterium avium complex disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease basal cell carcinoma breast cancer bronchiectasis cancer chronic fatigue syndrome chronic kidney disease complex partial epilepsy cone-rod dystrophy 2 cone-rod dystrophy cystic fibrosis disease of mental health embryoma encephalitis encephalomyelitis epilepsy hemochromatosis type 2 hemochromatosis type 2A hemochromatosis heroin dependence lesion of sciatic nerve lung disease middle cerebral artery infarction morphine dependence multiple sclerosis myelitis neuromyelitis optica obesity opiate dependence primary progressive multiple sclerosis progressive relapsing multiple sclerosis prostate cancer prostate carcinoma psychotic disorder sciatic neuropathy secondary progressive multiple sclerosis temporal lobe epilepsy visual epilepsy
Q96B97	SH3 domain-containing kinase-binding protein 1	SH3KBP1 CIN85	Homo sapiens (human)	13	4
Q96BA8	Cyclic AMP-responsive element-binding protein 3-like protein 1	CREB3L1 OASIS	Homo sapiens (human)	4	4
Q96BD0	Solute carrier organic anion transporter family member 4A1	SLCO4A1 OATP1 OATP4A1 OATPE SLC21A12	Homo sapiens (human)	2	1

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