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 **3526 - 3550** 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
P04920	Anion exchange protein 2	SLC4A2 AE2 EPB3L1 HKB3 MPB3L	Homo sapiens (human)	3	4
Q7Z2Y8	Interferon-induced very large GTPase 1	GVINP1 GVIN1 VLIG1	Homo sapiens (human)	3	1
C0LU32	MHC class I-related chain A (Fragment)	MICA	Homo sapiens (human)	3	0
Q9Y5F7	Protocadherin gamma-C4	PCDHGC4	Homo sapiens (human)	3	0
P14207	Folate receptor beta	FOLR2	Homo sapiens (human)	3	0	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 Ebola hemorrhagic fever Fleck corneal dystrophy Lyme disease Pick's disease Rett syndrome Reye syndrome Stevens-Johnson syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome benign mesothelioma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration cerebral folate receptor alpha deficiency childhood osteosarcoma chronic fatigue syndrome chronic myeloid leukemia colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis diverticulitis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma enthesopathy erythema multiforme fibromyalgia gestational diabetes granular cell carcinoma head and neck squamous cell carcinoma hematologic cancer hemolytic anemia hepatocellular carcinoma hyperhomocysteinemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease interstitial lung disease large intestine cancer lingual-facial-buccal dyskinesia liver cancer liver carcinoma localized scleroderma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma malignant mesothelioma malignant pleural mesothelioma maturity-onset diabetes of the young measles melanoma mitochondrial metabolism disease mitochondrial myopathy movement disease multiple myeloma multiple sclerosis myelitis myelomeningocele myocardial infarction neurodegenerative disease osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma postinflammatory pulmonary fibrosis pulmonary fibrosis rheumatoid arthritis scleroderma silent myocardial infarction skin melanoma spina bifida squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovitis systemic scleroderma temporal arteritis tenosynovitis tethered spinal cord syndrome tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uterine corpus cancer vascular disease
Q9H0V9	VIP36-like protein	LMAN2L VIPL	Homo sapiens (human)	3	10	agnosia attention deficit hyperactivity disorder bipolar disorder borderline personality disorder cerebral degeneration choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy intermittent explosive disorder lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary adenocarcinoma papillary renal cell carcinoma partial motor epilepsy pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 thyroid gland papillary carcinoma visual epilepsy
Q9P2C4	Transmembrane protein 181	TMEM181 GPR178 KIAA1423	Homo sapiens (human)	3	3
P30405	Peptidyl-prolyl cis-trans isomerase F, mitochondrial	PPIF CYP3	Homo sapiens (human)	3	9
O76082	Organic cation/carnitine transporter 2	SLC22A5 OCTN2	Homo sapiens (human)	3	6
P23280	Carbonic anhydrase 6	CA6	Homo sapiens (human)	3	13
P30559	Oxytocin receptor	OXTR	Homo sapiens (human)	3	1
P50416	Carnitine O-palmitoyltransferase 1, liver isoform	CPT1A CPT1	Homo sapiens (human)	3	1	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 D-bifunctional protein deficiency Niemann-Pick disease type C1 Niemann-Pick disease Pearson syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction alcoholic hepatitis alveolar rhabdomyosarcoma amnestic disorder beta thalassemia breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency cataract 4 multiple types cerebral degeneration chronic fatigue syndrome chronic kidney disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential thrombocythemia familial hyperlipidemia familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease isolated elevated serum creatine phosphokinase levels large intestine cancer liver cancer liver carcinoma liver cirrhosis lymphangioleiomyomatosis major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia osteoporosis placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis renal tubular acidosis retrograde amnesia sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction skin melanoma speech disorder steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency visual epilepsy
P02679	Fibrinogen gamma chain	FGG	Homo sapiens (human)	3	107
C0LZS2	MHC class I polypeptide-related sequence A (Fragment)	MICA	Homo sapiens (human)	3	0
Q6IS24	Polypeptide N-acetylgalactosaminyltransferase 17	GALNT17 WBSCR17	Homo sapiens (human)	3	0	allergic asthma asthma autism spectrum disorder autistic disorder intrinsic asthma
P45452	Collagenase 3	MMP13	Homo sapiens (human)	3	1
P32239	Gastrin/cholecystokinin type B receptor	CCKBR CCKRB	Homo sapiens (human)	3	0
P56937	3-keto-steroid reductase/17-beta-hydroxysteroid dehydrogenase 7	HSD17B7 17HSD7 SDR37C1	Homo sapiens (human)	3	0	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Zellweger syndrome adenocarcinoma adenoma adrenal gland cancer androgen insensitivity syndrome basal cell carcinoma breast cancer breast carcinoma breast ductal carcinoma cancer carcinoma cerebral degeneration choriocarcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis disorder of sexual development duodenum cancer duodenum disease embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis esophageal disease follicular adenoma gallbladder cancer gallbladder carcinoma glaucoma goiter heart cancer hereditary breast ovarian cancer syndrome hermaphroditism hyperandrogenism hypogonadotropic hypogonadism 23 with or without anosmia hypospadias invasive ductal carcinoma large intestine cancer leiomyoma microcystic adenoma multiple sclerosis myofibroma nodular prostate ovarian cancer ovarian carcinoma papillary adenoma peroxisomal disease peroxisome biogenesis disorder 1A pheochromocytoma placenta cancer polycystic ovary syndrome primary immunodeficiency disease prolactinoma prostate cancer prostate carcinoma prostatic adenoma pseudohermaphroditism sebaceous carcinoma small intestine cancer sporadic breast cancer steatotic liver disease stomach cancer stomach carcinoma stomach disease sweat gland cancer thymic carcinoma thymoma thyroid gland disease type 2 diabetes mellitus uterine corpus cancer uterine fibroid
Q9BZ71	Membrane-associated phosphatidylinositol transfer protein 3	PITPNM3 NIR1	Homo sapiens (human)	3	1
Q9BRK3	Matrix remodeling-associated protein 8	MXRA8	Homo sapiens (human)	3	2
Q9H8M5	Metal transporter CNNM2	CNNM2 ACDP2	Homo sapiens (human)	3	9
A0A0J9YWQ3	Alpha-2-antiplasmin (Fragment)	SERPINF2	Homo sapiens (human)	3	0
P47870	Gamma-aminobutyric acid receptor subunit beta-2	GABRB2	Homo sapiens (human)	3	0
O94875	Sorbin and SH3 domain-containing protein 2	SORBS2 ARGBP2 KIAA0777	Homo sapiens (human)	3	3
Q14865	AT-rich interactive domain-containing protein 5B	ARID5B DESRT MRF2	Homo sapiens (human)	3	1

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