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 **13876 - 13900** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q8CGY8	UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit	Ogt	Mus musculus (house mouse)	8	1
Q9BR11	Zinc finger SWIM domain-containing protein 1	ZSWIM1 C20orf162	Homo sapiens (human)	0	1
O15553	Pyrin	MEFV MEF TRIM20	Homo sapiens (human)	2	1
Q8IUN9	C-type lectin domain family 10 member A	CLEC10A CLECSF13 CLECSF14 HML	Homo sapiens (human)	3	1	B-cell lymphoma Crohn's colitis Crohn's disease Ebola hemorrhagic fever acquired immunodeficiency syndrome acrodermatitis adenosquamous carcinoma adult lymphoma allergic asthma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease asthma atopic dermatitis autosomal recessive distal hereditary motor neuronopathy 1 bipolar disorder breast cancer breast carcinoma cancer celiac disease central nervous system lymphoma centronuclear myopathy cervical adenocarcinoma cervical cancer cervix carcinoma childhood lymphoma cholesteatoma cholinergic urticaria congenital structural myopathy coronary artery disease dermatitis embryoma embryonal cancer germ cell and embryonal cancer germ cell cancer germinoma hepatocellular carcinoma human immunodeficiency virus infectious disease hypereosinophilic syndrome inflammatory bowel disease 1 inflammatory bowel disease influenza intrinsic asthma lateral sclerosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma melanoma motor neuron disease neurodegenerative disease obsolete malignant histiocytosis obsolete ymphosarcoma ovarian cancer ovarian carcinoma peripheral T-cell lymphoma polyp of middle ear progressive muscular atrophy prostate cancer prostate carcinoma rheumatoid arthritis schizophrenia skin melanoma squamous cell carcinoma teratocarcinoma tongue squamous cell carcinoma transient myeloproliferative syndrome tubular aggregate myopathy 1 ulcerative colitis viral infectious disease
Q15119	[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial	PDK2 PDHK2	Homo sapiens (human)	0	1
Q5JVG2	Zinc finger protein 484	ZNF484	Homo sapiens (human)	0	1
Q5NCE8	Magnesium transporter MRS2 homolog, mitochondrial	Mrs2 Gm902 Mrs2l	Mus musculus (house mouse)	0	1
P60764	Ras-related C3 botulinum toxin substrate 3	Rac3	Mus musculus (house mouse)	0	1
Q9ET78	Junctophilin-2	Jph2 Jp2	Mus musculus (house mouse)	0	1
Q15738	Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating	NSDHL H105E3	Homo sapiens (human)	0	1	Bloch-Sulzberger syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
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

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