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 **3051 - 3075** 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
H0YCG2	Lysosomal associated membrane protein 2 (Fragment)	LAMP2	Homo sapiens (human)	2	0
Q9NQC8	Intraflagellar transport protein 46 homolog	IFT46 C11orf2 C11orf60	Homo sapiens (human)	0	1
Q92542	Nicastrin	NCSTN KIAA0253	Homo sapiens (human)	28	31
Q96R05	Retinoid-binding protein 7	RBP7	Homo sapiens (human)	0	1
I6NWJ8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P02771	Alpha-fetoprotein	AFP HPAFP	Homo sapiens (human)	4	50
Q5HYI7	Metaxin-3	MTX3	Homo sapiens (human)	2	1
Q07837	Amino acid transporter heavy chain SLC3A1	SLC3A1 NBAT	Homo sapiens (human)	6	37	IgA glomerulonephritis Marfan syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy breast cancer breast carcinoma bulimia nervosa calcinosis calcium metabolism disease cancer chronic kidney disease colon carcinoma colorectal cancer congenital myasthenic syndrome 22 congenital ptosis coronary thrombosis cystinuria diabetes mellitus diabetic ketoacidosis distal myopathy epilepsy essential hypertension facioscapulohumeral muscular dystrophy galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease high grade glioma hypercalcemia hypertension hypoglycemia hypogonadism hypotonia-cystinuria syndrome interstitial nephritis kidney failure lactic acidosis limb-girdle muscular dystrophy muscular dystrophy myocardial infarction nephrocalcinosis nephrolithiasis nephrosclerosis obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy panic disorder phosphorus metabolism disease primary pulmonary hypertension prostate cancer prostate carcinoma ptosis pyelitis pyelonephritis renal hypertension renal infectious disease silent myocardial infarction situs inversus synovial sarcoma tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis urinary tract obstruction vesicoureteral reflux visual epilepsy
Q13938	Calcyphosin	CAPS	Homo sapiens (human)	2	1
Q9H488	GDP-fucose protein O-fucosyltransferase 1	POFUT1 FUT12 KIAA0180	Homo sapiens (human)	2	17	Dowling-Degos disease acrodermatitis actinic keratosis acute myocardial infarction bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery anomaly coronary thrombosis dermatitis gallbladder disease hepatocellular carcinoma invasive ductal carcinoma large intestine cancer liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcephaly myeloproliferative neoplasm myocardial infarction reticulate acropigmentation of Kitamura schizophrenia seborrheic keratosis silent myocardial infarction skin disease
Q96T88	E3 ubiquitin-protein ligase UHRF1	UHRF1 ICBP90 NP95 RNF106	Homo sapiens (human)	0	1
P18825	Alpha-2C adrenergic receptor	ADRA2C ADRA2L2 ADRA2RL2	Homo sapiens (human)	2	0
Q658U4	peptidylprolyl isomerase	DKFZp666D193	Homo sapiens (human)	2	0
Q92828	Coronin-2A	CORO2A IR10 WDR2	Homo sapiens (human)	0	1
Q9BZ71	Membrane-associated phosphatidylinositol transfer protein 3	PITPNM3 NIR1	Homo sapiens (human)	3	1
G1EMQ7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9Y6N5	Sulfide:quinone oxidoreductase, mitochondrial	SQOR SQRDL	Homo sapiens (human)	1	2
G3D6E4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
F1AQQ6	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P18621	Large ribosomal subunit protein uL22	RPL17	Homo sapiens (human)	0	1
Q8N9W5	Dynein axonemal assembly factor 3	DNAAF3 C19orf51	Homo sapiens (human)	1	1
O60437	Periplakin	PPL KIAA0568	Homo sapiens (human)	1	1
A0A5Q2WUN2	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q8IYX1	TBC1 domain family member 21	TBC1D21 MGCRABGAP	Homo sapiens (human)	0	1
Q75NT9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0

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