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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96B70	Leukocyte receptor cluster member 9	LENG9	0	1
Q96B49	Mitochondrial import receptor subunit TOM6 homolog	TOMM6 OBTP TOM6	4	2
Q96B45	BLOC-1-related complex subunit 7	BORCS7 C10orf32	0	1
Q96B36	Proline-rich AKT1 substrate 1	AKT1S1 PRAS40	3	2
Q96B26	Exosome complex component RRP43	EXOSC8 OIP2 RRP43	1	2
Q96B23	Protein ARK2N	ARK2N ARKL1 C18orf25	2	1
Q96B18	Dapper homolog 3	DACT3 RRR1	2	1
Q96B01	RAD51-associated protein 1	RAD51AP1 PIR51	1	2
Q96AY4	Tetratricopeptide repeat protein 28	TTC28 KIAA1043 TPRBK	5	1
Q96AY3	Peptidyl-prolyl cis-trans isomerase FKBP10	FKBP10 FKBP65	12	53
Q96AV8	Transcription factor E2F7	E2F7	1	1
Q96AT9	Ribulose-phosphate 3-epimerase	RPE	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
Q96AR9	PLOD2 protein (Fragment)	PLOD2	1	0
Q96AQ6	Pre-B-cell leukemia transcription factor-interacting protein 1	PBXIP1 HPIP	2	14
Q96AQ1	Coiled-coil domain-containing protein 74A	CCDC74A	1	1
Q96AP7	Endothelial cell-selective adhesion molecule	ESAM	5	28
Q96AP4	Zinc finger-containing ubiquitin peptidase 1	ZUP1 C6orf113 ZUFSP	0	1
Q96AM1	Mas-related G-protein coupled receptor member F	MRGPRF GPR140 GPR168 MRGF	1	0
Q96AH0	SOSS complex subunit B2	NABP1 OBFC2A SSB2	1	1
Q96AG4	Leucine-rich repeat-containing protein 59	LRRC59	0	1
Q96AE7	Tetratricopeptide repeat protein 17	TTC17	7	13
Q96AE4	Far upstream element-binding protein 1	FUBP1	9	1
Q96AD5	Patatin-like phospholipase domain-containing protein 2	PNPLA2 ATGL	4	2	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 Barth syndrome Chanarin-Dorfman syndrome Ehlers-Danlos syndrome Kuhnt-Junius degeneration Laron syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acanthosis nigricans achondroplasia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adenosarcoma adult liposarcoma age related macular degeneration agnosia anogenital venereal wart arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive congenital ichthyosis 1 bacterial sepsis bladder carcinoma bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease cartilage disease cavernous hemangioma celiac disease central nervous system cancer cerebral degeneration childhood liposarcoma childhood osteosarcoma cholecystitis chorioangioma chylomicron retention disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cone-rod dystrophy congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital generalized lipodystrophy congestive heart failure connective tissue disease coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder developmental coordination disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma endometrial hyperplasia endomyocardial fibrosis epithelioid leiomyosarcoma exudative vitreoretinopathy 1 exudative vitreoretinopathy eye disease familial combined hyperlipidemia familial hyperlipidemia familial lipoprotein lipase deficiency familial periodic paralysis familial retinoblastoma fibromyalgia fundus albipunctatus gestational diabetes gliosarcoma glomus tumor glucose intolerance glycogen storage disease II granular cell carcinoma heart disease hemangioma hepatoblastoma hepatocellular carcinoma high grade glioma histiocytoid hemangioma hyperinsulinism hyperlipoproteinemia type V hypertrophic cardiomyopathy ichthyosis impotence intramuscular hemangioma isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leiomyosarcoma leukostasis lipoatrophic diabetes mellitus lipodystrophy liposarcoma liver cancer lung benign neoplasm lung cancer lung carcinoma lymphangioma macular degeneration major depressive disorder melancholic depression melanoma microphthalmia mixed glioma mongolian spot myocardial infarction myopathy myositis myxoid leiomyosarcoma nasopharynx carcinoma nephroblastoma neuropathy neurotic disorder nicotine dependence obesity obsolete Matthew-Wood syndrome obsolete congenital ichthyosiform erythroderma obsolete melancholia ocular melanoma osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma peripheral nervous system disease pleomorphic liposarcoma polycystic ovary syndrome prediabetes syndrome premature ejaculation primary ciliary dyskinesia 1 primary ciliary dyskinesia proliferative diabetic retinopathy prostate cancer prostate carcinoma pseudoxanthoma elasticum psychologic dyspareunia rectal benign neoplasm rectum adenocarcinoma rectum cancer retinal disease retinitis pigmentosa retinitis retinoblastoma retinopathy of prematurity rhabdomyosarcoma rheumatoid arthritis schizophrenia sensorineural hearing loss silent myocardial infarction skin melanoma steatotic liver disease stomach cancer stomach carcinoma systemic primary carnitine deficiency disease trilateral retinoblastoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
Q96AC1	Fermitin family homolog 2	FERMT2 KIND2 MIG2 PLEKHC1	0	1
Q96A99	Pentraxin-4	PTX4 C16orf38	2	0

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