GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q96RN1	Testis anion transporter 1	SLC26A8 TAT1	2	2
Q8TE54	Anion exchange transporter	SLC26A7 SUT2	2	3
Q9BXS9	Solute carrier family 26 member 6	SLC26A6	2	0
P58743	Prestin	SLC26A5 PRES	2	0
O43511	Pendrin	SLC26A4 PDS	0	1
P40879	Chloride anion exchanger	SLC26A3 DRA	3	0
P50443	Sulfate transporter	SLC26A2 DTD DTDST	3	0	Baraitser-Winter syndrome Bartter disease Clostridium difficile colitis Conn's syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Pendred Syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome achondrogenesis type IB achondroplasia adenocarcinoma adenoma arthritis arthropathy atelosteogenesis auditory system disease autosomal recessive osteopetrosis 7 benign mesothelioma branchiootic syndrome breast cancer cancer chondrodysplasia punctata cleft palate clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure cryptorchidism cystic lymphangioma diarrhea diastrophic dysplasia disease of metabolism dyshormonogenic goiter embryoma endometritis fibrosarcoma follicular adenoma inguinal hernia irritable bowel syndrome isolated cleft palate juvenile rheumatoid arthritis large intestine cancer laryngostenosis lingual-facial-buccal dyskinesia lung benign neoplasm lung cancer lung non-small cell carcinoma malignant mesothelioma mastitis microcystic adenoma movement disease mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia 4 multiple epiphyseal dysplasia neurocirculatory asthenia omphalocele orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis osteochondrodysplasia osteopetrosis osteoporosis osteosclerosis otosclerosis papillary adenoma placental insufficiency polyhydramnios primary hyperaldosteronism scoliosis sensorineural hearing loss spinal cord disease spondylolysis stomach cancer stomach carcinoma umbilical hernia
Q9H2B4	Sulfate anion transporter 1	SLC26A1 SAT1	2	0
P12236	ADP/ATP translocase 3	SLC25A6 AAC3 ANT3	1	1
Q5H9E4	Solute carrier family 25 member 53	SLC25A53 MCART6	1	1
P05141	ADP/ATP translocase 2	SLC25A5 AAC2 ANT2	0	1
Q8N5S1	Mitochondrial carrier protein SCaMC-3L	SLC25A41	1	1
P12235	ADP/ATP translocase 1	SLC25A4 AAC1 ANT1	0	1
Q6PIV7	Solute carrier family 25 member 34	SLC25A34	1	1
Q9BSK2	Solute carrier family 25 member 33	SLC25A33	0	1
Q5SVS4	Kidney mitochondrial carrier protein 1	SLC25A30 KMCP1 UCP6	1	2
Q00325	Solute carrier family 25 member 3	SLC25A3 PHC	0	1
Q6NUK1	Mitochondrial adenyl nucleotide antiporter SLC25A24	SLC25A24 APC1 MCSC1 SCAMC1	0	1
Q9BV35	Mitochondrial adenyl nucleotide antiporter SLC25A23	SLC25A23 APC2 MCSC2 SCAMC3	1	1
Q9H936	Mitochondrial glutamate carrier 1	SLC25A22 GC1	0	1
Q9HC21	Mitochondrial thiamine pyrophosphate carrier	SLC25A19 DNC MUP1	1	2
O43808	Peroxisomal membrane protein PMP34	SLC25A17 PMP34	0	1
P16260	Solute carrier family 25 member 16	SLC25A16 GDA	3	1
Q9Y619	Mitochondrial ornithine transporter 1	SLC25A15 ORC1 ORNT1	0	1
Q9UJS0	Electrogenic aspartate/glutamate antiporter SLC25A13, mitochondrial	SLC25A13	3	1

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