GlyCosmos Portal

Displaying entries **1501 - 1525** of **18496** in total

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NY65	Tubulin alpha-8 chain	TUBA8 TUBAL2	0	1
Q9NY64	Solute carrier family 2, facilitated glucose transporter member 8	SLC2A8 GLUT8 GLUTX1	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
Q9NY61	Protein AATF	AATF CHE1 DED	4	1
Q9NY47	Voltage-dependent calcium channel subunit alpha-2/delta-2	CACNA2D2 KIAA0558	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
Q9NY46	Sodium channel protein type 3 subunit alpha	SCN3A KIAA1356 NAC3	8	1
Q9NY37	Acid-sensing ion channel 5	ASIC5 ACCN5 HINAC	2	1
Q9NY35	Claudin domain-containing protein 1	CLDND1 C3orf4	2	7
Q9NY33	Dipeptidyl peptidase 3	DPP3	2	2
Q9NY28	Probable polypeptide N-acetylgalactosaminyltransferase 8	GALNT8	3	0	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C
Q9NY27	Serine/threonine-protein phosphatase 4 regulatory subunit 2	PPP4R2	1	1
Q9NY25	C-type lectin domain family 5 member A	CLEC5A CLECSF5 MDL1	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
Q9NY15	Stabilin-1	STAB1 FEEL1 KIAA0246	29	62
Q9NY12	H/ACA ribonucleoprotein complex subunit 1	GAR1 NOLA1	0	1
Q9NXZ6	BMP and activin membrane-bound inhibitor homolog	nma	1	0
Q9NXZ2	Probable ATP-dependent RNA helicase DDX43	DDX43 HAGE	0	1
Q9NXX6	Non-structural maintenance of chromosomes element 4 homolog A	NSMCE4A C10orf86	1	1
Q9NXV6	CDKN2A-interacting protein	CDKN2AIP CARF	40	4
Q9NXV2	BTB/POZ domain-containing protein KCTD5	KCTD5	0	1
Q9NXR8	Inhibitor of growth protein 3	ING3	1	1
Q9NXR1	Nuclear distribution protein nudE homolog 1	NDE1 NUDE	0	1
Q9NXL6	SID1 transmembrane family member 1	SIDT1	8	0
Q9NXH9	tRNA (guanine(26)-N(2))-dimethyltransferase	TRMT1	0	1
Q9NXH8	Torsin-4A	TOR4A C9orf167	1	9
Q9NXG6	Transmembrane prolyl 4-hydroxylase	P4HTM PH4	6	10
Q9NXG2	THUMP domain-containing protein 1	THUMPD1	2	1

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