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 **121801 - 121825** 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
Q19676	Amino acid transporter transmembrane domain-containing protein	CELE_F21D12.3	Caenorhabditis elegans	2	0
Q22397	Amino acid transporter protein 6	aat-6	Caenorhabditis elegans	2	0
Q7YQK3	Amino acid transporter heavy chain SLC3A2	SLC3A2	Oryctolagus cuniculus (rabbit)	3	0
P10852	Amino acid transporter heavy chain SLC3A2	Slc3a2 Mdu1	Mus musculus (house mouse)	8	12
Q794F9	Amino acid transporter heavy chain SLC3A2	Slc3a2	Rattus norvegicus (Norway rat)	8	12
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
Q91WV7	Amino acid transporter heavy chain SLC3A1	Slc3a1 Nbat	Mus musculus (house mouse)	7	14
Q64319	Amino acid transporter heavy chain SLC3A1	Slc3a1 Nbat	Rattus norvegicus (Norway rat)	7	0
M0QX44	Amino acid transporter (Fragment)	SLC1A5	Homo sapiens (human)	1	0
A2APL7	Amino acid transporter	Slc1a2	Mus musculus (house mouse)	2	0
Q3UYK6	Amino acid transporter	Slc1a2	Mus musculus (house mouse)	2	0
M0QXM4	Amino acid transporter	SLC1A5	Homo sapiens (human)	1	0
Q8C3T7	Amino acid transporter	Slc1a3	Mus musculus (house mouse)	2	0
Q71UA6	Amino acid transporter	SLC1A5	Homo sapiens (human)	1	0
Q543U3	Amino acid transporter	Slc1a3	Mus musculus (house mouse)	2	0
Q3UTP8	Amino acid transporter	Slc1a4	Mus musculus (house mouse)	2	0
Q9ESU8	Amino acid transporter	Slc1a4	Mus musculus (house mouse)	2	0
Q5SSP3	Amino acid transporter	Slc1a4	Mus musculus (house mouse)	2	0
Q8BXT5	Amino acid transporter	Slc1a4	Mus musculus (house mouse)	2	0
Q3US35	Amino acid transporter	Slc1a4	Mus musculus (house mouse)	2	0
A2APL5	Amino acid transporter	Slc1a2	Mus musculus (house mouse)	2	0
Q8C7W8	Amino acid transporter	Slc1a3	Mus musculus (house mouse)	2	0
Q3USU5	Amino acid transporter	Slc1a2	Mus musculus (house mouse)	2	0
X2D841	Amino acid transporter	Slc1a2	Mus musculus (house mouse)	2	0

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