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 **4226 - 4250** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
Q7L592	Protein arginine methyltransferase NDUFAF7, mitochondrial	NDUFAF7 C2orf56	Homo sapiens (human)	3	1
A0A7D9C126	MHC Class I chain-related protein	MICA	Homo sapiens (human)	3	0
P01137	Transforming growth factor beta-1 proprotein	TGFB1 TGFB	Homo sapiens (human)	3	10
Q19T08	Endothelial cell-specific chemotaxis regulator	ECSCR ECSM2	Homo sapiens (human)	3	3
Q7Z388	Probable C-mannosyltransferase DPY19L4	DPY19L4	Homo sapiens (human)	3	10
P23526	Adenosylhomocysteinase	AHCY SAHH	Homo sapiens (human)	3	2
A0A7D9C101	MHC Class I chain-related protein	MICA	Homo sapiens (human)	3	0
Q9NX78	Protein O-mannosyl-transferase TMEM260	TMEM260 C14orf101	Homo sapiens (human)	3	2	B-cell lymphoma Langerhans-cell histiocytosis acute myeloid leukemia alcohol dependence alcohol use disorder cancer double outlet right ventricle embryoma kidney failure lymphoma non-Hodgkin lymphoma obsolete ymphosarcoma reticulosarcoma ventricular septal defect
Q15256	Receptor-type tyrosine-protein phosphatase R	PTPRR ECPTP PTPRQ	Homo sapiens (human)	3	1
Q16625	Occludin	OCLN	Homo sapiens (human)	3	1
Q8N684	Cleavage and polyadenylation specificity factor subunit 7	CPSF7	Homo sapiens (human)	3	1
P16662	UDP-glucuronosyltransferase 2B7	UGT2B7 UGTB2B9	Homo sapiens (human)	3	52	agnosia bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardia cancer cardiovascular system disease clear cell renal cell carcinoma colorectal cancer colorectal carcinoma congestive heart failure diarrhea embryoma endometrial cancer endometrial carcinoma epilepsy gallbladder disease heart disease hepatitis hepatocellular carcinoma kidney cancer large intestine cancer leukopenia liver cancer liver carcinoma liver disease renal carcinoma renal cell carcinoma sarcomatoid carcinoma sickle cell anemia transitional cell carcinoma tuberculosis urinary bladder cancer uterine corpus cancer visual epilepsy
Q9NUI1	Peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing]	DECR2 PDCR SDR17C1	Homo sapiens (human)	3	2
Q14678	KN motif and ankyrin repeat domain-containing protein 1	KANK1 ANKRD15 KANK KIAA0172	Homo sapiens (human)	3	1
P59922	Putative olfactory receptor 2B8	OR2B8P OR2B8	Homo sapiens (human)	3	0
P02794	Ferritin heavy chain	FTH1 FTH FTHL6	Homo sapiens (human)	3	3
Q8IZL2	Mastermind-like protein 2	MAML2 KIAA1819	Homo sapiens (human)	3	1
Q86W42	THO complex subunit 6 homolog	THOC6 WDR58	Homo sapiens (human)	3	1
Q13467	Frizzled-5	FZD5 C2orf31	Homo sapiens (human)	3	2
Q8WWF5	E3 ubiquitin-protein ligase ZNRF4	ZNRF4 RNF204	Homo sapiens (human)	3	0
Q9Y6W8	Inducible T-cell costimulator	ICOS AILIM	Homo sapiens (human)	3	0
C8C064	Bone morphogenetic protein 2	BMP2	Homo sapiens (human)	3	0
Q53H54	tRNA wybutosine-synthesizing protein 2 homolog	TRMT12 TRM12 TYW2	Homo sapiens (human)	3	1
P52803	Ephrin-A5	EFNA5 EPLG7 LERK7	Homo sapiens (human)	3	11	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Ambras type hypertrichosis universalis congenita IGSF1 deficiency syndrome Norum disease Pick's disease Reye syndrome Tangier disease abdominal aortic aneurysm abetalipoproteinemia acquired immunodeficiency syndrome acute lymphoblastic leukemia acute myeloid leukemia adult medulloblastoma amyotrophic lateral sclerosis anencephaly arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness breast cancer breast carcinoma bulimia nervosa cancer cardiovascular system disease cataract cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood medulloblastoma chondrosarcoma choreaacanthocytosis colitis conduct disorder congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 coronary artery disease cystic fibrosis diffuse large B-cell lymphoma embryoma enophthalmos familial hypobetalipoproteinemia 1 gastric ulcer gastroenteritis heart disease hemiplegia hepatocellular carcinoma human immunodeficiency virus infectious disease hypobetalipoproteinemia hypolipoproteinemia hypothyroidism ileitis ileocolitis infertility inflammatory bowel disease 1 inflammatory bowel disease liver cancer lymphoblastic lymphoma medulloblastoma medullomyoblastoma melanotic medulloblastoma myxedema nicotine dependence nutmeg liver obsessive-compulsive disorder obsolete exophthalmos orbital disease peripheral vascular disease progressive muscular atrophy prostate cancer prostate carcinoma schizophrenia sclerocornea senile cataract spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia ulcerative colitis
Q99707	Methionine synthase	MTR	Homo sapiens (human)	3	2

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