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 **113026 - 113050** of **126547** in total

« First

‹ Prev

…

4518

4519

4520

4521

4522

4523

4524

4525

4526

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P69891	Hemoglobin subunit gamma-1	HBG1	Homo sapiens (human)	0	1
P0CG48	Polyubiquitin-C	UBC	Homo sapiens (human)	0	1
P13984	General transcription factor IIF subunit 2	GTF2F2 RAP30	Homo sapiens (human)	1	1
P47934	Carnitine O-acetyltransferase	Crat	Mus musculus (house mouse)	0	1
Q9BWD1	Acetyl-CoA acetyltransferase, cytosolic	ACAT2 ACTL	Homo sapiens (human)	1	1	amyotrophic lateral sclerosis androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis beta-ketothiolase deficiency breast cancer cholecystolithiasis choledocholithiasis cholelithiasis choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease hepatitis C hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease liver cancer nutmeg liver papillary renal cell carcinoma premature menopause progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma syndromic X-linked intellectual disability type 10 ulcerative colitis
Q8TCT0	Ceramide kinase	CERK KIAA1646	Homo sapiens (human)	0	1	Kaposi's sarcoma breast cancer breast carcinoma cancer colitis gastroenteritis ileitis ileocolitis microphthalmia neuroblastoma obesity obsolete Matthew-Wood syndrome schizophrenia 10 schizophrenia
O75420	GRB10-interacting GYF protein 1	GIGYF1 CDS2 PERQ1	Homo sapiens (human)	2	1
Q4DCN7	DUF2817 domain-containing protein	Tc00.1047053506943.80	Trypanosoma cruzi strain CL Brener	0	1
Q9FMM3	Protein ESSENTIAL FOR POTEXVIRUS ACCUMULATION 1	EXA1 MUSE11 PSIG1	Arabidopsis thaliana (thale cress)	0	1
Q96LL4	Uncharacterized protein C8orf48	C8orf48	Homo sapiens (human)	3	1
Q5TBC7	Bcl-2-like protein 15	BCL2L15 C1orf178	Homo sapiens (human)	0	1
Q4D966	Uncharacterized protein	Tc00.1047053506725.10	Trypanosoma cruzi strain CL Brener	0	1
P30084	Enoyl-CoA hydratase, mitochondrial	ECHS1	Homo sapiens (human)	1	1	3-methylglutaconic aciduria Balo concentric sclerosis Hailey-Hailey disease Leigh disease Rothmund-Thomson syndrome adrenoleukodystrophy alcohol dependence alcohol use disorder anemia 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 breast cancer breast carcinoma cancer cardiomyopathy central nervous system disease childhood onset GLUT1 deficiency syndrome 2 chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy congenital nystagmus congenital ptosis cutis laxa disease of metabolism dissociated nystagmus dystonia embryoma endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy focal hand dystonia fundus albipunctatus generalized dystonia giant cell glioblastoma glioblastoma hepatitis A hepatitis hepatocellular carcinoma high grade glioma hypertrichosis hypertrophic cardiomyopathy hypertropia inherited metabolic disorder lactic acidosis leukodystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma macrocytic anemia mal de Meleda mechanical strabismus mitochondrial metabolism disease narcolepsy nervous system disease neuropathy nonpapillary renal cell carcinoma obesity ophthalmoplegia optic atrophy overnutrition papillary renal cell carcinoma pathologic nystagmus peripheral nervous system disease periventricular leukomalacia ptosis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal carcinoma renal cell carcinoma restrictive dermopathy retinitis pigmentosa sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 ventricular septal defect visual epilepsy
P36873	Serine/threonine-protein phosphatase PP1-gamma catalytic subunit	PPP1CC	Homo sapiens (human)	0	1
Q4DIR3	Protein kinase, putative	Tc00.1047053511661.100	Trypanosoma cruzi strain CL Brener	0	1
V5BD32	CCT-theta	TCDM_05987	Trypanosoma cruzi Dm28c	0	1
Q9R0H0	Peroxisomal acyl-coenzyme A oxidase 1	Acox1 Acox Paox	Mus musculus (house mouse)	0	1
Q96S44	EKC/KEOPS complex subunit TP53RK	TP53RK C20orf64 PRPK	Homo sapiens (human)	0	1
P17425	Hydroxymethylglutaryl-CoA synthase, cytoplasmic	Hmgcs1 Hmgcs	Rattus norvegicus (Norway rat)	0	1
Q8IYL9	Psychosine receptor	GPR65 TDAG8	Homo sapiens (human)	3	1
V5DBK9	Thioredoxin-like fold domain-containing protein	TCDM_06958	Trypanosoma cruzi Dm28c	0	1
V5AWG2	Uncharacterized protein	TCDM_06586	Trypanosoma cruzi Dm28c	0	1
Q15102	Platelet-activating factor acetylhydrolase IB subunit alpha1	PAFAH1B3 PAFAHG	Homo sapiens (human)	0	1	intellectual disability learning disability
Q5FW97	phosphopyruvate hydratase	EG433182 Eno1	Mus musculus (house mouse)	0	1
Q8N283	Ankyrin repeat domain-containing protein 35	ANKRD35	Homo sapiens (human)	3	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements