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 **15801 - 15825** of **18496** in total

« First

‹ Prev

…

629

630

631

632

633

634

635

636

637

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol ▲	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
A0A0S2Z534	Metal cation symporter ZIP14 (Fragment)	SLC39A14	Homo sapiens (human)	3	0
E5RGA7	Solute carrier family 39 member 14 (Fragment)	SLC39A14	Homo sapiens (human)	1	0
E5RIP4	Solute carrier family 39 member 14 (Fragment)	SLC39A14	Homo sapiens (human)	3	0
A0A0S2Z5C8	Metal cation symporter ZIP14	SLC39A14	Homo sapiens (human)	3	0
A0A0S2Z5Z7	Metal cation symporter ZIP14 (Fragment)	SLC39A14	Homo sapiens (human)	3	0
E5RFZ8	Solute carrier family 39 member 14 (Fragment)	SLC39A14	Homo sapiens (human)	1	0
Q6P5W5	Zinc transporter ZIP4	SLC39A4 ZIP4	Homo sapiens (human)	2	1
Q6ZMH5	Zinc transporter ZIP5	SLC39A5 ZIP5	Homo sapiens (human)	6	5
Q13433	Zinc transporter ZIP6	SLC39A6 LIV1 ZIP6	Homo sapiens (human)	23	18
Q92504	Zinc transporter SLC39A7	SLC39A7 HKE4 RING5	Homo sapiens (human)	1	1
Q9C0K1	Metal cation symporter ZIP8	SLC39A8 BIGM103 ZIP8	Homo sapiens (human)	2	2	Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease achondroplasia acute chest syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood androgen insensitivity syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy astigmatism atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autonomic neuropathy bacterial sepsis breast cancer breast carcinoma cancer central nervous system disease cerebral infarction cerebrovascular disease childhood leukemia colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type IIn congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease craniosynostosis dermatitis diabetes mellitus diabetic ketoacidosis dissociated nystagmus dystonia epilepsy essential hypertension focal hand dystonia generalized dystonia hemochromatosis hydrocephalus hyperopia hypertension hypertropia idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability iron metabolism disease kwashiorkor large intestine cancer learning disability left ventricular noncompaction leukemia macrocytic anemia marasmus mechanical strabismus mitochondrial metabolism disease mitochondrial myopathy nervous system disease neuroblastoma nicotine dependence nutrition disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus protein-energy malnutrition pulmonary tuberculosis schizophrenia sensorineural hearing loss spontaneous ocular nystagmus strabismus systemic lupus erythematosus tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis visual epilepsy
Q9NUM3	Zinc transporter ZIP9	SLC39A9 ZIP9	Homo sapiens (human)	4	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
P08195	Amino acid transporter heavy chain SLC3A2	SLC3A2 MDU1	Homo sapiens (human)	5	147
A0A7P0TAN7	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
F5GZI0	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
F5GZS6	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
F5H056	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
A0A7P0TBF8	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
A0A7P0Z4A0	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
A0A7P0T8F1	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
A0A7P0Z4P5	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
A0A7P0T9F7	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
A0A7P0T8U7	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0
A0A7P0TAS6	Solute carrier family 3 member 2	SLC3A2	Homo sapiens (human)	3	0

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements