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 **13701 - 13725** 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
P48547	Potassium voltage-gated channel subfamily C member 1	KCNC1	Homo sapiens (human)	2	0
Q99456	Keratin, type I cytoskeletal 12	KRT12	Homo sapiens (human)	0	1
Q7LGC8	Carbohydrate sulfotransferase 3	CHST3	Homo sapiens (human)	6	4	Bannayan-Riley-Ruvalcaba syndrome Bartter disease Conn's syndrome Cowden syndrome Desbuquois dysplasia Hailey-Hailey disease Laron syndrome Larsen syndrome Larsen-like syndrome B3GAT3 type Ollier disease Rothmund-Thomson syndrome SOST-related sclerosing bone dysplasia Schwartz-Jampel syndrome 1 Silverman-Handmaker type dyssegmental dysplasia Sjogren's syndrome Waterhouse-Friderichsen syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia acute promyelocytic leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma agnosia alcoholic hepatitis alcoholic liver cirrhosis amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atrophy of testis autoimmune hepatitis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease blastomycosis breast cancer breast carcinoma buphthalmos cancer cardiomyopathy cardiovascular system disease choriocarcinoma cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital adrenal hyperplasia coronary artery disease craniosynostosis cutis laxa cystadenoma dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis diastrophic dysplasia embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis enterocele esotropia essential hypertension fibrosarcoma follicular adenoma heart disease hepatitis hereditary multiple exostoses humeroradial synostosis hydrocephalus hydrophthalmos hyperopia hypertension hypertrophic cardiomyopathy hypogonadotropic hypogonadism 23 with or without anosmia inclusion body myositis intrahepatic cholestasis isolated cleft palate juvenile glaucoma keratoconjunctivitis sicca leiomyoma liver cirrhosis lung small cell carcinoma mal de Meleda microcystic adenoma mitral valve insufficiency mitral valve prolapse mitral valve stenosis monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia myofibroma neurogenic arthropathy obesity obsolete type 1 diabetes mellitus 9 obstructive hydrocephalus osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma ovarian hyperstimulation syndrome papillary adenoma paracoccidioidomycosis patent foramen ovale placenta cancer polycystic ovary syndrome postural orthostatic tachycardia syndrome primary hyperaldosteronism primary pulmonary hypertension progressive familial intrahepatic cholestasis progressive pseudorheumatoid arthropathy of childhood pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss spondyloepiphyseal dysplasia congenita spondyloepiphyseal dysplasia with congenital joint dislocations strabismic amblyopia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency tricuspid valve stenosis 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 type 2 diabetes mellitus uterine corpus cancer uterine fibroid varicose veins ventricular septal defect
Q8TF74	WAS/WASL-interacting protein family member 2	WIPF2 WICH WIRE	Homo sapiens (human)	7	2
P15391	B-lymphocyte antigen CD19	CD19	Homo sapiens (human)	5	0
Q8IY18	Structural maintenance of chromosomes protein 5	SMC5 KIAA0594 SMC5L1	Homo sapiens (human)	1	2
Q9MY53	Leucocyte antigen B (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q8NHU6	Tudor domain-containing protein 7	TDRD7 PCTAIRE2BP	Homo sapiens (human)	2	1
P42025	Beta-centractin	ACTR1B CTRN2	Homo sapiens (human)	1	1
Q7Z3Z9	L1 cell adhesion molecule (Fragment)	L1CAM	Homo sapiens (human)	2	0
Q99677	Lysophosphatidic acid receptor 4	LPAR4 GPR23 LPA4 P2RY9	Homo sapiens (human)	4	0
Q96BQ5	Coiled-coil domain-containing protein 127	CCDC127	Homo sapiens (human)	1	2
Q9UQ72	Pregnancy-specific beta-1-glycoprotein 11	PSG11 PSG13 PSG14	Homo sapiens (human)	4	1
E3Q1J1	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9H074	Polyadenylate-binding protein-interacting protein 1	PAIP1	Homo sapiens (human)	1	1
P25788	Proteasome subunit alpha type-3	PSMA3 HC8 PSC8	Homo sapiens (human)	1	2
Q9H1J1	Regulator of nonsense transcripts 3A	UPF3A RENT3A UPF3	Homo sapiens (human)	0	1
G3V150	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3GAT3	Homo sapiens (human)	1	0
Q92888	Rho guanine nucleotide exchange factor 1	ARHGEF1	Homo sapiens (human)	0	1
Q6V4Z4	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q10588	ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2	BST1	Homo sapiens (human)	4	25	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 Burkitt lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome acute monocytic leukemia acute myeloid leukemia allergic asthma asthma autism spectrum disorder autistic disorder benign mesothelioma benign pleural mesothelioma bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic lymphocytic leukemia depressive disorder dysthymic disorder embryoma essential hypertension hypertension inflammatory and toxic neuropathy intrinsic asthma lung benign neoplasm lung cancer lung carcinoma lung disease major depressive disorder malignant mesothelioma malignant pleural mesothelioma melancholic depression neurotic disorder obsolete melancholia ovarian cancer ovarian carcinoma paroxysmal nocturnal hemoglobinuria pleural tuberculosis pneumonia prion disease prostate cancer prostate carcinoma tuberculosis
E1XUD0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q13131	5'-AMP-activated protein kinase catalytic subunit alpha-1	PRKAA1 AMPK1	Homo sapiens (human)	0	1
Q14314	Fibroleukin	FGL2	Homo sapiens (human)	7	126
O15178	T-box transcription factor T	TBXT T	Homo sapiens (human)	4	1

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