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 **5451 - 5475** 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
Q8N2A8	Mitochondrial cardiolipin hydrolase	PLD6	Homo sapiens (human)	2	2
Q562R1	Beta-actin-like protein 2	ACTBL2	Homo sapiens (human)	2	2
A8MYU2	Potassium channel subfamily U member 1	KCNU1 KCNMA3 KCNMC1 SLO3	Homo sapiens (human)	2	4
Q9NYV7	Taste receptor type 2 member 16	TAS2R16	Homo sapiens (human)	2	0
Q9HB03	Very long chain fatty acid elongase 3	ELOVL3 CIG30	Homo sapiens (human)	2	0	amnestic disorder atopic dermatitis dermatitis diabetes mellitus diabetic ketoacidosis ichthyosis prostate cancer prostate carcinoma retrograde amnesia type 2 diabetes mellitus
Q6IE81	Protein Jade-1	JADE1 KIAA1807 PHF17	Homo sapiens (human)	2	2
Q9NZ01	Very-long-chain enoyl-CoA reductase	TECR GPSN2 SC2	Homo sapiens (human)	2	1	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
Q8NGT2	Olfactory receptor 13J1	OR13J1	Homo sapiens (human)	2	0
Q01718	Adrenocorticotropic hormone receptor	MC2R ACTHR	Homo sapiens (human)	2	0
Q8TDG4	Helicase POLQ-like	HELQ HEL308	Homo sapiens (human)	2	7
P22033	Methylmalonyl-CoA mutase, mitochondrial	MMUT MUT	Homo sapiens (human)	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 Creutzfeldt-Jakob disease Kallmann syndrome Pick's disease Reye syndrome Sheehan syndrome acoustic neuroma actinic keratosis acute pancreatitis adult medulloblastoma adult oligodendroglioma agranulocytosis ampulla of Vater carcinoma anemia angiomatous meningioma 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 bacterial sepsis basal cell carcinoma basal ganglia disease benign meningioma blepharospasm bone osteosarcoma branched-chain keto acid dehydrogenase kinase deficiency breast cancer bronchus cancer bronchus carcinoma bulbar polio cancer cardiomyopathy cataract 40 central nervous system cancer cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma chromophobe renal cell carcinoma clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma congestive heart failure conversion disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dissociative disorder dystonia embryoma endomyocardial fibrosis epilepsy familial retinoblastoma fibrous meningioma focal hand dystonia giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma homocystinuria hypertrophic cardiomyopathy hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism in situ carcinoma influenza inherited metabolic disorder intellectual disability interstitial nephritis intraorbital meningioma intraventricular meningioma inverted follicular keratosis isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency keratoacanthoma kidney failure large intestine cancer laryngeal squamous cell carcinoma learning disability leukopenia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia mal de Meleda medulloblastoma medullomyoblastoma melanoacanthoma melanotic medulloblastoma meningioma meningothelial meningioma methylmalonic acidemia cblA type methylmalonic acidemia cblB type methylmalonic acidemia due to transcobalamin receptor defect methylmalonic acidemia methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency microcystic meningioma microphthalmia mitochondrial metabolism disease mixed glioma mixed oligodendroglioma-astrocytoma nasopharynx carcinoma neuroblastoma neutropenia nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome olfactory groove meningioma oligodendroglioma optic atrophy osteosarcoma palmoplantar keratosis pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis pancytopenia panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma patent foramen ovale penis carcinoma in situ pituitary adenoma poliomyelitis primary immunodeficiency disease propionic acidemia psammomatous meningioma pyelonephritis renal carcinoma renal cell carcinoma renal infectious disease retinoblastoma sarcomatoid renal cell carcinoma seborrheic keratosis secretory meningioma severe congenital neutropenia skin disease skin squamous cell carcinoma spinal meningioma stomach cancer stomach carcinoma syndactyly thrombocytopenia thyroid gland anaplastic carcinoma thyroid gland papillary carcinoma transcobalamin II deficiency transitional cell carcinoma transitional meningioma trilateral retinoblastoma tropical sprue tuberculosis urea cycle disorder visual epilepsy
P0CW18	Serine protease 56	PRSS56	Homo sapiens (human)	2	2
Q13508	Ecto-ADP-ribosyltransferase 3	ART3 TMART	Homo sapiens (human)	2	9	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
A0A0M3R835	Rhodopsin	RHO	Homo sapiens (human)	2	0
P51587	Breast cancer type 2 susceptibility protein	BRCA2 FACD FANCD1	Homo sapiens (human)	2	5
O60907	F-box-like/WD repeat-containing protein TBL1X	TBL1X TBL1	Homo sapiens (human)	2	1
Q14995	Nuclear receptor subfamily 1 group D member 2	NR1D2	Homo sapiens (human)	2	1
P47902	Homeobox protein CDX-1	CDX1	Homo sapiens (human)	2	1
I3L1J1	Sex hormone-binding globulin	SHBG	Homo sapiens (human)	2	0
Q8NDW8	Tetratricopeptide repeat protein 21A	TTC21A STI2	Homo sapiens (human)	2	1
Q8NEF9	Serum response factor-binding protein 1	SRFBP1	Homo sapiens (human)	2	1
Q8TBG9	Synaptoporin	SYNPR	Homo sapiens (human)	2	0
A0A1B0GVP3	Cathepsin D	CTSD	Homo sapiens (human)	2	0
Q7Z618	EMR2 protein	EMR2	Homo sapiens (human)	2	0
O95407	Tumor necrosis factor receptor superfamily member 6B	TNFRSF6B DCR3 TR6	Homo sapiens (human)	2	1

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