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 **12151 - 12175** 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
Q4CW22	DNA/RNA-binding protein Alba-like domain-containing protein	Tc00.1047053504001.20	Trypanosoma cruzi strain CL Brener	0	1
Q9Z1K5	E3 ubiquitin-protein ligase ARIH1	Arih1 Ari Ubch7bp Uip77	Mus musculus (house mouse)	0	1
Q6ZQJ9	Condensin complex subunit 2 (Fragment)	Ncaph Brrn1 mKIAA0074	Mus musculus (house mouse)	0	1
P32189	Glycerol kinase	GK	Homo sapiens (human)	1	1	Aland Island eye disease Becker muscular dystrophy Duchenne muscular dystrophy Kallmann syndrome Klinefelter syndrome Laron syndrome Patau syndrome Sheehan syndrome X-linked adrenal hypoplasia congenita achondroplasia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy chromosome Xp21 deletion syndrome cone-rod dystrophy congenital muscular dystrophy coronary artery disease diabetes mellitus distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypercholesterolemia fundus albipunctatus galactokinase deficiency galactosemia glycerol kinase deficiency hypertropia hypoglycemia hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism intellectual disability isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency learning disability limb-girdle muscular dystrophy mechanical strabismus muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy ophthalmoplegia osteoporosis panhypopituitarism placental insufficiency retinitis pigmentosa rippling muscle disease 2 strabismus tuberculosis type 2 diabetes mellitus
Q94547	Regulator of gene activity	Rga Not2	Drosophila melanogaster (fruit fly)	0	1
Q12051	Geranylgeranyl pyrophosphate synthase BTS1	BTS1	Saccharomyces cerevisiae S288C	1	1
Q8WVZ7	E3 ubiquitin-protein ligase RNF133	RNF133	Homo sapiens (human)	2	1
O15726	Casein kinase I	CK1	Plasmodium falciparum Dd2	0	1
P47884	Olfactory receptor 1D4	OR1D4	Homo sapiens (human)	2	1
Q8N111	Cell cycle exit and neuronal differentiation protein 1	CEND1 BM88	Homo sapiens (human)	2	1
Q6QNY0	Biogenesis of lysosome-related organelles complex 1 subunit 3	BLOC1S3 BLOS3	Homo sapiens (human)	0	1
B9QND8	Signal peptidase	BN1205_031760	Toxoplasma gondii VEG	0	1
Q9WU65	Glycerol kinase 2	Gk2 Gk-rs2 Gkrs2	Mus musculus (house mouse)	0	1
Q4KL80	Fibronectin	Fn1	Mus musculus (house mouse)	1	1
Q96L92	Sorting nexin-27	SNX27 KIAA0488	Homo sapiens (human)	0	1
Q9Y6G5	COMM domain-containing protein 10	COMMD10	Homo sapiens (human)	0	1
O75689	Arf-GAP with dual PH domain-containing protein 1	ADAP1 CENTA1	Homo sapiens (human)	0	1
Q4DF20	short-chain 2-methylacyl-CoA dehydrogenase	Tc00.1047053507001.80	Trypanosoma cruzi strain CL Brener	0	1
Q4D3E3	Succinate dehydrogenase subunit	Tc00.1047053508397.40	Trypanosoma cruzi strain CL Brener	0	1
Q96CW9	Netrin-G2	NTNG2 KIAA1857 LMNT2	Homo sapiens (human)	5	1
Q4DPP9	Bridge-like lipid transfer protein family member 1 N-terminal domain-containing protein	Tc00.1047053506743.60	Trypanosoma cruzi strain CL Brener	0	1
P53814	Smoothelin	SMTN SMSMO	Homo sapiens (human)	6	1
Q9MAH8	Transcription factor TCP3	TCP3	Arabidopsis thaliana (thale cress)	0	1
Q9NWV4	CXXC motif containing zinc binding protein	CZIB C1orf123	Homo sapiens (human)	0	1
Q13506	NGFI-A-binding protein 1	NAB1	Homo sapiens (human)	3	1

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