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 **4651 - 4675** 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
P46471	26S proteasome regulatory subunit 7	Psmc2 Mss1	Mus musculus (house mouse)	1	2
Q9Y4B4	Helicase ARIP4	RAD54L2 ARIP4 KIAA0809	Homo sapiens (human)	7	2
A8CG34	Nuclear envelope pore membrane protein POM 121C	POM121C	Homo sapiens (human)	35	2
Q96N06	Spermatogenesis-associated protein 33	SPATA33 C16orf55	Homo sapiens (human)	3	2
O60513	Beta-1,4-galactosyltransferase 4	B4GALT4	Homo sapiens (human)	4	2	prostate cancer prostate carcinoma
Q8CG79	Apoptosis-stimulating of p53 protein 2	Tp53bp2 Aspp2 Trp53bp2	Mus musculus (house mouse)	4	2
P24369	Peptidyl-prolyl cis-trans isomerase B	Ppib	Mus musculus (house mouse)	1	2
P19783	Cytochrome c oxidase subunit 4 isoform 1, mitochondrial	Cox4i1 Cox4 Cox4a Coxiv	Mus musculus (house mouse)	1	2
Q5SYD0	Unconventional myosin-Id	Myo1d	Mus musculus (house mouse)	1	2
P68033	Actin, alpha cardiac muscle 1	Actc1 Actc	Mus musculus (house mouse)	3	2
Q14683	Structural maintenance of chromosomes protein 1A	SMC1A DXS423E KIAA0178 SB1.8 SMC1 SMC1L1	Homo sapiens (human)	3	2
P09912	Interferon alpha-inducible protein 6	IFI6 G1P3	Homo sapiens (human)	1	2
Q6UX15	Layilin	LAYN	Homo sapiens (human)	4	2	arthritis arthropathy bronchus cancer bronchus carcinoma cancer chronic obstructive pulmonary disease colitis colon cancer colonic benign neoplasm colorectal cancer embryoma gastroenteritis gliosarcoma glomerulonephritis high grade glioma ileitis ileocolitis kidney disease large intestine cancer lung cancer lung carcinoma mixed glioma nephritis osteoarthritis
Q9Y5S2	Serine/threonine-protein kinase MRCK beta	CDC42BPB KIAA1124	Homo sapiens (human)	2	2
O55017	Voltage-dependent N-type calcium channel subunit alpha-1B	Cacna1b Cach5 Cacnl1a5 Cchn1a	Mus musculus (house mouse)	5	2
Q9Z1S8	GRB2-associated-binding protein 2	Gab2	Mus musculus (house mouse)	2	2
Q5RJH6	Nonsense-mediated mRNA decay factor SMG7	Smg7 Est1c Kiaa0250	Mus musculus (house mouse)	4	2
Q9EP82	tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4	Wdr4	Mus musculus (house mouse)	1	2
Q7Z6K1	THAP domain-containing protein 5	THAP5	Homo sapiens (human)	1	2
O08749	Dihydrolipoyl dehydrogenase, mitochondrial	Dld	Mus musculus (house mouse)	2	2
Q8TE56	A disintegrin and metalloproteinase with thrombospondin motifs 17	ADAMTS17	Homo sapiens (human)	7	2
Q8IY17	Patatin-like phospholipase domain-containing protein 6	PNPLA6 NTE	Homo sapiens (human)	1	2	Bardet-Biedl syndrome Boucher-Neuhauser syndrome Brooke-Spiegler syndrome Charcot-Marie-Tooth disease type 5 Henoch-Schoenlein purpura Kallmann syndrome Klinefelter syndrome Laron syndrome Laurence-Moon syndrome Leber congenital amaurosis MASA syndrome MYH-9 related disease Mast syndrome Oliver-McFarlane syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Peutz-Jeghers syndrome SPOAN syndrome Sheehan syndrome Stargardt disease Troyer syndrome achondroplasia adiposis dolorosa alopecia alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive distal hereditary motor neuronopathy 1 autosomal recessive polycystic kidney disease biliary tract disease blindness blue cone monochromacy cancer cataract cavernous hemangioma central nervous system disease cerebellar ataxia cerebellar disease chorioangioma coloboma cone-rod dystrophy congenital nystagmus craniosynostosis critical illness polyneuropathy cryptorchidism dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic neuropathy diabetic polyneuropathy dissociated nystagmus dysthymic disorder embryoma epilepsy focal epilepsy fundus albipunctatus fundus dystrophy glomus tumor gynecomastia hemangioma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia histiocytoid hemangioma hypersensitivity vasculitis hypertrophy of breast hypertropia 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 ichthyosis infant gynecomastia inflammatory and toxic neuropathy intellectual disability intramuscular hemangioma 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 keratosis follicularis kidney failure lateral sclerosis learning disability lipomatosis liver cirrhosis lymphangioma major depressive disorder mechanical strabismus melancholic depression meningoencephalitis migraine without aura mongolian spot motor neuron disease multiple symmetric lipomatosis muscular atrophy nervous system disease neuroblastoma neurodegenerative disease neuropathy neurotic disorder obesity obsolete asthenopia obsolete congenital ichthyosiform erythroderma obsolete melancholia obsolete multiple symmetrical lipomatosis obstructive jaundice ophthalmoplegia optic atrophy panhypopituitarism paraplegia partial motor epilepsy pathologic nystagmus peripheral nervous system disease placental insufficiency polycystic kidney disease 4 polydactyly polyneuropathy progressive muscular atrophy pseudoxanthoma elasticum recurrent hypersomnia retinal degeneration retinitis pigmentosa sensorineural hearing loss sick building syndrome speech disorder spontaneous ocular nystagmus steatotic liver disease strabismus type 2 diabetes mellitus viral infectious disease visual epilepsy von Hippel-Lindau disease
Q9Y2T3	Guanine deaminase	GDA KIAA1258	Homo sapiens (human)	1	2
Q9CS42	Ribose-phosphate pyrophosphokinase 2	Prps2	Mus musculus (house mouse)	1	2
Q9NRR5	Ubiquilin-4	UBQLN4 C1orf6 CIP75 UBIN	Homo sapiens (human)	2	2

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