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 **17701 - 17725** 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
Q02410	Amyloid-beta A4 precursor protein-binding family A member 1	APBA1 MINT1 X11	Homo sapiens (human)	0	1
O00213	Amyloid beta precursor protein binding family B member 1	APBB1 FE65 RIR	Homo sapiens (human)	1	1
Q06481	Amyloid beta precursor like protein 2	APLP2 APPL2	Homo sapiens (human)	12	24
P51693	Amyloid beta precursor like protein 1	APLP1	Homo sapiens (human)	7	3
Q86WK7	Amphoterin-induced protein 3	AMIGO3 ALI3 KIAA1851	Homo sapiens (human)	5	2
Q86SJ2	Amphoterin-induced protein 2	AMIGO2 ALI1	Homo sapiens (human)	9	6
Q86WK6	Amphoterin-induced protein 1	AMIGO1 ALI2 AMIGO KIAA1163	Homo sapiens (human)	5	2
P15514	Amphiregulin	AREG AREGB SDGF	Homo sapiens (human)	10	3
Q9UBD6	Ammonium transporter Rh type C	RHCG C15orf6 CDRC2 PDRC2 RHGK	Homo sapiens (human)	1	0
Q9H310	Ammonium transporter Rh type B	RHBG	Homo sapiens (human)	1	0
Q02094	Ammonium transporter Rh type A	RHAG RH50	Homo sapiens (human)	3	1
Q6Q4G3	Aminopeptidase Q	LVRN AQPEP	Homo sapiens (human)	8	0
Q9UQQ1	Aminopeptidase NAALADL1	NAALADL1 NAALADASEL NAALADL	Homo sapiens (human)	7	0
P15144	Aminopeptidase N	ANPEP APN CD13 PEPN	Homo sapiens (human)	18	199
Q9H4A4	Aminopeptidase B	RNPEP APB	Homo sapiens (human)	2	1
Q03154	Aminoacylase-1	ACY1	Homo sapiens (human)	0	1
Q13155	Aminoacyl tRNA synthase complex-interacting multifunctional protein 2	AIMP2 JTV1	Homo sapiens (human)	0	1
Q12904	Aminoacyl tRNA synthase complex-interacting multifunctional protein 1	AIMP1 EMAP2 SCYE1	Homo sapiens (human)	1	1
P08195	Amino acid transporter heavy chain SLC3A2	SLC3A2 MDU1	Homo sapiens (human)	5	147
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
M0QX44	Amino acid transporter (Fragment)	SLC1A5	Homo sapiens (human)	1	0
M0QXM4	Amino acid transporter	SLC1A5	Homo sapiens (human)	1	0
Q71UA6	Amino acid transporter	SLC1A5	Homo sapiens (human)	1	0
P27338	Amine oxidase [flavin-containing] B	MAOB	Homo sapiens (human)	0	1
P21397	Amine oxidase [flavin-containing] A	MAOA	Homo sapiens (human)	1	1

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