GlyCosmos Portal

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GlyConnect	April 19, 2023
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **121576 - 121600** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9BR11	Zinc finger SWIM domain-containing protein 1	ZSWIM1 C20orf162	Homo sapiens (human)	1
Q15119	[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial	PDK2 PDHK2	Homo sapiens (human)	1
Q5JVG2	Zinc finger protein 484	ZNF484	Homo sapiens (human)	1
Q5NCE8	Magnesium transporter MRS2 homolog, mitochondrial	Mrs2 Gm902 Mrs2l	Mus musculus (house mouse)	1
P60764	Ras-related C3 botulinum toxin substrate 3	Rac3	Mus musculus (house mouse)	1
Q9ET78	Junctophilin-2	Jph2 Jp2	Mus musculus (house mouse)	1
Q15738	Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating	NSDHL H105E3	Homo sapiens (human)	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)	1
P0CG48	Polyubiquitin-C	UBC	Homo sapiens (human)	1
P47934	Carnitine O-acetyltransferase	Crat	Mus musculus (house mouse)	1
Q8TCT0	Ceramide kinase	CERK KIAA1646	Homo sapiens (human)	1	Kaposi's sarcoma breast cancer breast carcinoma cancer colitis gastroenteritis ileitis ileocolitis microphthalmia neuroblastoma obesity obsolete Matthew-Wood syndrome schizophrenia 10 schizophrenia
Q4DCN7	DUF2817 domain-containing protein	Tc00.1047053506943.80	Trypanosoma cruzi strain CL Brener	1
Q9FMM3	Protein ESSENTIAL FOR POTEXVIRUS ACCUMULATION 1	EXA1 MUSE11 PSIG1	Arabidopsis thaliana (thale cress)	1
Q5TBC7	Bcl-2-like protein 15	BCL2L15 C1orf178	Homo sapiens (human)	1
Q4D966	Uncharacterized protein	Tc00.1047053506725.10	Trypanosoma cruzi strain CL Brener	1
P36873	Serine/threonine-protein phosphatase PP1-gamma catalytic subunit	PPP1CC	Homo sapiens (human)	1
Q4DIR3	Protein kinase, putative	Tc00.1047053511661.100	Trypanosoma cruzi strain CL Brener	1
V5BD32	CCT-theta	TCDM_05987	Trypanosoma cruzi Dm28c	1
Q9R0H0	Peroxisomal acyl-coenzyme A oxidase 1	Acox1 Acox Paox	Mus musculus (house mouse)	1
Q96S44	EKC/KEOPS complex subunit TP53RK	TP53RK C20orf64 PRPK	Homo sapiens (human)	1
P17425	Hydroxymethylglutaryl-CoA synthase, cytoplasmic	Hmgcs1 Hmgcs	Rattus norvegicus (Norway rat)	1
V5DBK9	Thioredoxin-like fold domain-containing protein	TCDM_06958	Trypanosoma cruzi Dm28c	1
V5AWG2	Uncharacterized protein	TCDM_06586	Trypanosoma cruzi Dm28c	1
Q15102	Platelet-activating factor acetylhydrolase IB subunit alpha1	PAFAH1B3 PAFAHG	Homo sapiens (human)	1	intellectual disability learning disability
Q5FW97	phosphopyruvate hydratase	EG433182 Eno1	Mus musculus (house mouse)	1

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