GlyCosmos Portal

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UniProt ID	Protein Name ▼	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q02410	Amyloid-beta A4 precursor protein-binding family A member 1	APBA1 MINT1 X11	0	1
O00213	Amyloid beta precursor protein binding family B member 1	APBB1 FE65 RIR	1	1
Q06481	Amyloid beta precursor like protein 2	APLP2 APPL2	12	24
P51693	Amyloid beta precursor like protein 1	APLP1	7	3
Q86WK7	Amphoterin-induced protein 3	AMIGO3 ALI3 KIAA1851	5	2
Q86SJ2	Amphoterin-induced protein 2	AMIGO2 ALI1	9	6
Q86WK6	Amphoterin-induced protein 1	AMIGO1 ALI2 AMIGO KIAA1163	5	2
P15514	Amphiregulin	AREG AREGB SDGF	10	3
Q9UBD6	Ammonium transporter Rh type C	RHCG C15orf6 CDRC2 PDRC2 RHGK	1	0
Q9H310	Ammonium transporter Rh type B	RHBG	1	0
Q02094	Ammonium transporter Rh type A	RHAG RH50	3	1
Q6Q4G3	Aminopeptidase Q	LVRN AQPEP	8	0
Q9UQQ1	Aminopeptidase NAALADL1	NAALADL1 NAALADASEL NAALADL	7	0
P15144	Aminopeptidase N	ANPEP APN CD13 PEPN	18	199
Q9H4A4	Aminopeptidase B	RNPEP APB	2	1
Q03154	Aminoacylase-1	ACY1	0	1
Q13155	Aminoacyl tRNA synthase complex-interacting multifunctional protein 2	AIMP2 JTV1	0	1
Q12904	Aminoacyl tRNA synthase complex-interacting multifunctional protein 1	AIMP1 EMAP2 SCYE1	1	1
P08195	Amino acid transporter heavy chain SLC3A2	SLC3A2 MDU1	5	147
Q07837	Amino acid transporter heavy chain SLC3A1	SLC3A1 NBAT	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	1	0
M0QXM4	Amino acid transporter	SLC1A5	1	0
Q71UA6	Amino acid transporter	SLC1A5	1	0
P27338	Amine oxidase [flavin-containing] B	MAOB	0	1
P21397	Amine oxidase [flavin-containing] A	MAOA	1	1

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