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 **126351 - 126375** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q13201	Multimerin-1	MMRN1 ECM EMILIN4 GPIA* MMRN	Homo sapiens (human)	29	68
P05164	Myeloperoxidase	MPO	Homo sapiens (human)	8	69
P01019	Angiotensinogen	AGT SERPINA8	Homo sapiens (human)	9	69
A0A1D5RMA8	Cadherin 16 (Fragment)	Cdh16	Mus musculus (house mouse)	1	69
A0A1D5RMB7	Cadherin 16 (Fragment)	Cdh16	Mus musculus (house mouse)	1	69
Q3TPA4	Cadherin 16	Cdh16	Mus musculus (house mouse)	3	69
Q546A8	Ksp-cadherin	Cdh16	Mus musculus (house mouse)	3	69
Q8C730	Cadherin 16	Cdh16	Mus musculus (house mouse)	3	69
O88338	Cadherin-16	Cdh16	Mus musculus (house mouse)	3	69
P20239	Zona pellucida sperm-binding protein 2	Zp2 Zp-2 Zpa	Mus musculus (house mouse)	7	70
Q99523	Sortilin	SORT1	Homo sapiens (human)	9	70
Q08431	Lactadherin	MFGE8	Homo sapiens (human)	7	70
P12763	Alpha-2-HS-glycoprotein	AHSG FETUA	Bos taurus (cattle)	9	70
P28906	Hematopoietic progenitor cell antigen CD34	CD34	Homo sapiens (human)	10	71
P09486	SPARC	SPARC ON	Homo sapiens (human)	2	71
P11117	Lysosomal acid phosphatase	ACP2	Homo sapiens (human)	13	72
P54802	Alpha-N-acetylglucosaminidase	NAGLU UFHSD1	Homo sapiens (human)	7	72	Alzheimer's disease Burkitt lymphoma Charcot-Marie-Tooth disease axonal type 2V Clouston syndrome Dent disease Fanconi syndrome Glanzmann's thrombasthenia Kluver-Bucy syndrome Legg-Calve-Perthes disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma amnestic disorder amyloidosis appendicitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrophic gastritis autistic disorder cancer cardiovascular system disease cholera chronic kidney disease chronic pyelonephritis cone-rod dystrophy congestive heart failure coronary artery disease cribriform carcinoma cystinosis cystitis dementia dentatorubral-pallidoluysian atrophy diabetes mellitus diabetic ketoacidosis diarrhea embryoma epilepsy essential thrombocythemia focal segmental glomerulosclerosis follicular adenoma fundus albipunctatus glomerulonephritis granular cell carcinoma gray platelet syndrome heart disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy 1 intellectual disability kidney disease kidney failure learning disability lipoid nephrosis liver cirrhosis lysosomal storage disease malignant pleural mesothelioma microcystic adenoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma myelodysplastic syndrome nephritis nephrosis neuroblastoma neurodegenerative disease oculocerebrorenal syndrome oculocutaneous albinism type IA osteochondrodysplasia otitis media panic disorder papillary adenoma parapsoriasis platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 progressive familial intrahepatic cholestasis 1 progressive myoclonus epilepsy prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole pyoureter qualitative platelet defect renal osteodystrophy retinitis pigmentosa retrograde amnesia sensorineural hearing loss spondyloepimetaphyseal dysplasia, Sponastrime type stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 trigonitis tubular adenocarcinoma type 2 diabetes mellitus viral infectious disease visual epilepsy
Q92823	Neuronal cell adhesion molecule	NRCAM KIAA0343	Homo sapiens (human)	22	72
Q62635	Mucin-2 (Fragment)	Muc2	Rattus norvegicus (Norway rat)	18	73
O95497	Pantetheinase	VNN1	Homo sapiens (human)	7	73	B-cell lymphoma Evans' syndrome Fanconi syndrome allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis autoimmune thrombocytopenic purpura cancer cardiovascular system disease celiac disease chronic kidney disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease cystinosis disease of metabolism embryoma essential hypertension gastroenteritis heart disease hydronephrosis hypertension ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma large intestine cancer malaria obsolete ymphosarcoma obstructive nephropathy parapsoriasis psoriasis pustulosis of palm and sole renal osteodystrophy spondyloepimetaphyseal dysplasia, Sponastrime type steatotic liver disease ulcerative colitis ureteral obstruction
P12273	Prolactin-inducible protein	PIP GCDFP15 GPIP4	Homo sapiens (human)	1	74
P25391	Laminin subunit alpha-1	LAMA1 LAMA	Homo sapiens (human)	22	74
O60635	Tetraspanin-1	TSPAN1	Homo sapiens (human)	4	74
Q86VB7	Scavenger receptor cysteine-rich type 1 protein M130	CD163 M130	Homo sapiens (human)	11	74
P01012	Ovalbumin	SERPINB14	Gallus gallus (chicken)	1	74

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