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 **3226 - 3250** 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
P29474	Nitric oxide synthase 3	NOS3	Homo sapiens (human)	4	2
O43670	BUB3-interacting and GLEBS motif-containing protein ZNF207	ZNF207 BUGZ	Homo sapiens (human)	23	2
P04908	Histone H2A type 1-B/E	H2AC4 H2AC8 H2AFA H2AFM HIST1H2AB HIST1H2AE	Homo sapiens (human)	2	2
Q6R327	Rapamycin-insensitive companion of mTOR	RICTOR KIAA1999	Homo sapiens (human)	4	2
Q13393	Phospholipase D1	PLD1	Homo sapiens (human)	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acral lentiginous melanoma acute myocardial infarction adult respiratory distress syndrome allergic asthma amnestic disorder anaplastic astrocytoma arthritis arthropathy asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bone osteosarcoma brain infarction breast cancer breast carcinoma cancer candidiasis carcinoma central nervous system cancer cerebral degeneration childhood cerebral astrocytoma childhood osteosarcoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma complex partial epilepsy congestive heart failure coronary thrombosis dementia diabetes mellitus disseminated intravascular coagulation embryoma epilepsy fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma gliosarcoma high grade glioma hydronephrosis ileitis ileocolitis immune system disease inguinal hernia intrinsic asthma juvenile pilocytic astrocytoma large intestine cancer malignant astrocytoma melanoma microphthalmia middle cerebral artery infarction mitral valve insufficiency mitral valve prolapse mitral valve stenosis mixed glioma multiple sclerosis myocardial infarction newborn respiratory distress syndrome nodular prostate nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome oral candidiasis osteosarcoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma patent foramen ovale pilocytic astrocytoma pneumonia postural orthostatic tachycardia syndrome primary immunodeficiency disease prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pterygium purpura fulminans relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma temporal lobe epilepsy tricuspid atresia tricuspid valve insufficiency tricuspid valve prolapse type 2 diabetes mellitus urethral diverticulum visual epilepsy
Q5VYJ5	MAM and LDL-receptor class A domain-containing protein 1	MALRD1 C10orf112 DIET1	Homo sapiens (human)	5	2
Q8N3Z0	Inactive serine protease 35	PRSS35 C6orf158	Homo sapiens (human)	2	2
P20042	Eukaryotic translation initiation factor 2 subunit 2	EIF2S2 EIF2B	Homo sapiens (human)	1	2
Q8NH55	Olfactory receptor 52E5	OR52E5	Homo sapiens (human)	2	2
Q8N135	Leucine-rich repeat LGI family member 4	LGI4 LGIL3	Homo sapiens (human)	2	2
Q9BTX1	Nucleoporin NDC1	NDC1 TMEM48	Homo sapiens (human)	3	2
P27695	DNA repair nuclease/redox regulator APEX1	APEX1 APE APE1 APEX APX HAP1 REF1	Homo sapiens (human)	1	2
P29353	SHC-transforming protein 1	SHC1 SHC SHCA	Homo sapiens (human)	1	2
Q13136	Liprin-alpha-1	PPFIA1 LIP1	Homo sapiens (human)	1	2
Q9H069	Dynein regulatory complex subunit 3	DRC3 LRRC48	Homo sapiens (human)	2	2
O95817	BAG family molecular chaperone regulator 3	BAG3 BIS	Homo sapiens (human)	21	2
O95498	Pantetheine hydrolase VNN2	VNN2	Homo sapiens (human)	7	2	Fanconi syndrome atopic dermatitis bone osteosarcoma cancer cystinosis disease of metabolism embryoma giant cell glioblastoma glioblastoma high grade glioma malaria osteosarcoma parapsoriasis psoriasis pustulosis of palm and sole spondyloepimetaphyseal dysplasia, Sponastrime type
Q9UKL0	REST corepressor 1	RCOR1 KIAA0071 RCOR	Homo sapiens (human)	3	2
Q9UKX7	Nuclear pore complex protein Nup50	NUP50 NPAP60L	Homo sapiens (human)	6	2
Q9Y3I0	RNA-splicing ligase RtcB homolog	RTCB C22orf28	Homo sapiens (human)	2	2
P18510	Interleukin-1 receptor antagonist protein	IL1RN IL1F3 IL1RA	Homo sapiens (human)	1	2
Q15435	Protein phosphatase 1 regulatory subunit 7	PPP1R7 SDS22	Homo sapiens (human)	1	2
Q9Y617	Phosphoserine aminotransferase	PSAT1 PSA	Homo sapiens (human)	1	2
P26358	DNA (cytosine-5)-methyltransferase 1	DNMT1 AIM CXXC9 DNMT	Homo sapiens (human)	1	2
Q8IWW6	Rho GTPase-activating protein 12	ARHGAP12	Homo sapiens (human)	1	2

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