GlyCosmos Portal

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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 **118526 - 118550** 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
Q9NY12	H/ACA ribonucleoprotein complex subunit 1	GAR1 NOLA1	Homo sapiens (human)	0	1
Q9NY15	Stabilin-1	STAB1 FEEL1 KIAA0246	Homo sapiens (human)	29	62
Q9NY25	C-type lectin domain family 5 member A	CLEC5A CLECSF5 MDL1	Homo sapiens (human)	4	0	Japanese encephalitis Mycoplasma pneumoniae pneumonia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis bone osteosarcoma brain glioblastoma multiforme central nervous system cancer cholesteatoma dengue disease dengue hemorrhagic fever giant cell glioblastoma glioblastoma gliosarcoma high grade glioma mixed glioma osteoarthritis osteosarcoma polyp of middle ear viral infectious disease yellow fever
Q9NY27	Serine/threonine-protein phosphatase 4 regulatory subunit 2	PPP4R2	Homo sapiens (human)	1	1
Q9NY28	Probable polypeptide N-acetylgalactosaminyltransferase 8	GALNT8	Homo sapiens (human)	3	0	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C
Q9NY33	Dipeptidyl peptidase 3	DPP3	Homo sapiens (human)	2	2
Q9NY35	Claudin domain-containing protein 1	CLDND1 C3orf4	Homo sapiens (human)	2	7
Q9NY37	Acid-sensing ion channel 5	ASIC5 ACCN5 HINAC	Homo sapiens (human)	2	1
Q9NY46	Sodium channel protein type 3 subunit alpha	SCN3A KIAA1356 NAC3	Homo sapiens (human)	8	1
Q9NY47	Voltage-dependent calcium channel subunit alpha-2/delta-2	CACNA2D2 KIAA0558	Homo sapiens (human)	11	6	absence epilepsy agnosia alternating hemiplegia of childhood autonomic neuropathy bipolar I disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebellar ataxia cerebellar disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 21 dissociated nystagmus embryoma epilepsy hypertropia idiopathic generalized epilepsy large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maple syrup urine disease mechanical strabismus nasopharynx carcinoma nervous system disease ophthalmoplegia pathologic nystagmus primary cutaneous amyloidosis prostate cancer prostate carcinoma sensorineural hearing loss sick sinus syndrome spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability type 10
Q9NY61	Protein AATF	AATF CHE1 DED	Homo sapiens (human)	4	1
Q9NY64	Solute carrier family 2, facilitated glucose transporter member 8	SLC2A8 GLUT8 GLUTX1	Homo sapiens (human)	1	0	cancer congenital hypothyroidism diabetic ketoacidosis hypothyroidism multiple myeloma myxedema obsolete type 1 diabetes mellitus 9 steatotic liver disease type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
Q9NY65	Tubulin alpha-8 chain	TUBA8 TUBAL2	Homo sapiens (human)	0	1
Q9NY72	Sodium channel regulatory subunit beta-3	SCN3B KIAA1158	Homo sapiens (human)	4	0
Q9NY74	Ewing's tumor-associated antigen 1	ETAA1 ETAA16	Homo sapiens (human)	1	1
Q9NY91	Probable glucose sensor protein SLC5A4	SLC5A4 SAAT1 SGLT3	Homo sapiens (human)	1	0
Q9NY97	N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2	B3GNT2 B3GALT7 B3GNT1	Homo sapiens (human)	8	21	Graves' disease Walker-Warburg syndrome acute myocardial infarction cancer congenital muscular dystrophy-dystroglycanopathy type A1 coronary thrombosis hyperthyroidism myocardial infarction parapsoriasis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole schizophrenia silent myocardial infarction thyrotoxicosis transitional cell carcinoma
Q9NY99	Gamma-2-syntrophin	SNTG2	Homo sapiens (human)	1	2
Q9NYA4	Myotubularin-related protein 4	MTMR4 KIAA0647 ZFYVE11	Homo sapiens (human)	1	1	anterior horn cell disease benign mesothelioma herpes simplex malignant mesothelioma muscular atrophy
Q9NYB0	Telomeric repeat-binding factor 2-interacting protein 1	TERF2IP DRIP5 RAP1	Homo sapiens (human)	2	1
Q9NYB5	Solute carrier organic anion transporter family member 1C1	SLCO1C1 OATP14 OATP1C1 OATPF SLC21A14	Homo sapiens (human)	5	1
Q9NYB9	Abl interactor 2	ABI2 ARGBPIA	Homo sapiens (human)	5	1
Q9NYC9	Dynein axonemal heavy chain 9	DNAH9 DNAH17L DNEL1 KIAA0357	Homo sapiens (human)	1	1
Q9NYD6	Homeobox protein Hox-C10	HOXC10 HOX3I	Homo sapiens (human)	3	1
Q9NYF0	Dapper homolog 1	DACT1 DPR1 HNG3	Homo sapiens (human)	1	1

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