GlyCosmos Portal

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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 **113001 - 113025** 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
Q5S003	Sperm-associated antigen 17	Spag17	Mus musculus (house mouse)	2	1
Q96KW2	POM121-like protein 2	POM121L2 POM121L	Homo sapiens (human)	2	1
Q9NW81	Distal membrane-arm assembly complex protein 2	DMAC2 ATP5SL	Homo sapiens (human)	0	1
P11464	Pregnancy-specific beta-1-glycoprotein 1	PSG1 B1G1 PSBG1 PSGGA	Homo sapiens (human)	8	1
Q4DST7	60S ribosomal protein L32, putative	Tc00.1047053510769.90	Trypanosoma cruzi strain CL Brener	0	1
Q4DE88	poly(A)-specific ribonuclease	Tc00.1047053510535.60	Trypanosoma cruzi strain CL Brener	0	1
Q15583	Homeobox protein TGIF1	TGIF1 TGIF	Homo sapiens (human)	0	1
Q9UBV8	Peflin	PEF1 ABP32	Homo sapiens (human)	0	1
B2RPU2	Pleckstrin homology domain-containing family D member 1	Plekhd1	Mus musculus (house mouse)	0	1
Q4DPH9	Proteasome activator complex subunit 4 C-terminal domain-containing protein (Fragment)	Tc00.1047053510861.14	Trypanosoma cruzi strain CL Brener	0	1
A0A0H2UHQ9	Synaptopodin	Synpo Myoz3	Rattus norvegicus (Norway rat)	0	1
P53999	Activated RNA polymerase II transcriptional coactivator p15	SUB1 PC4 RPO2TC1	Homo sapiens (human)	3	1
Q64433	10 kDa heat shock protein, mitochondrial	Hspe1	Mus musculus (house mouse)	0	1
O70194	Eukaryotic translation initiation factor 3 subunit D	Eif3d Eif3s7	Mus musculus (house mouse)	0	1
K2N0W4	60S ribosomal protein L4, putative	MOQ_003083	Trypanosoma cruzi marinkellei	0	1
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

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