GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
A0A6Q8PHD1	Alpha-galactosidase	GLA	2	0
A0A6Q8PFA9	Alpha-galactosidase	GLA	2	0
V9GYN5	Alpha-galactosidase	GLA	1	0
Q53Y83	Alpha-galactosidase	GLA	2	0
A0A6Q8PHM8	Alpha-galactosidase	GLA	2	0
A0A3B3IRU3	Alpha-galactosidase	GLA	1	0
Q5VSY0	G kinase-anchoring protein 1	GKAP1 GKAP42	2	1
P32189	Glycerol kinase	GK	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
Q5T442	Gap junction gamma-2 protein	GJC2 GJA12	1	1
P17302	Gap junction alpha-1 protein	GJA1 GJAL	0	1
Q14161	ARF GTPase-activating protein GIT2	GIT2 KIAA0148	10	3
Q9Y2X7	ARF GTPase-activating protein GIT1	GIT1	4	2
P48546	Gastric inhibitory polypeptide receptor	GIPR	2	0
Q8TF65	PDZ domain-containing protein GIPC2	GIPC2	0	1
O14908	PDZ domain-containing protein GIPC1	GIPC1 C19orf3 GIPC RGS19IP1	0	1
Q9BRT9	DNA replication complex GINS protein SLD5	GINS4 SLD5	0	1
Q9BRX5	DNA replication complex GINS protein PSF3	GINS3 PSF3	0	1
Q9Y248	DNA replication complex GINS protein PSF2	GINS2 PSF2	0	1
Q14691	DNA replication complex GINS protein PSF1	GINS1 KIAA0186 PSF1	0	1
Q9NU53	Glycoprotein integral membrane protein 1	GINM1 C6orf72	14	9
P0DJR0	GTPase IMAP family member GIMD1	GIMD1	0	1
Q8ND71	GTPase IMAP family member 8	GIMAP8 IAN9 IANT	0	1
Q8NHV1	GTPase IMAP family member 7	GIMAP7 IAN7	1	2
Q6Y7W6	GRB10-interacting GYF protein 2	GIGYF2 KIAA0642 PERQ2 TNRC15	8	2
O75420	GRB10-interacting GYF protein 1	GIGYF1 CDS2 PERQ1	2	1

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