GlyCosmos Portal

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Displaying entries **109501 - 109525** 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
Q8IXQ9	Electron transfer flavoprotein beta subunit lysine methyltransferase	ETFBKMT C12orf72 METTL20	Homo sapiens (human)	0	1
Q8IXS0	Protein FAM217A	FAM217A C6orf146	Homo sapiens (human)	0	1
Q8IXS8	Hyccin 2	HYCC2 FAM126B	Homo sapiens (human)	2	1
Q8IXT1	DNA damage-induced apoptosis suppressor protein	DDIAS C11orf82 NOXIN	Homo sapiens (human)	0	1
Q8IXT5	RNA-binding protein 12B	RBM12B	Homo sapiens (human)	2	2
Q8IXV7	Kelch domain-containing protein 8B	KLHDC8B	Homo sapiens (human)	0	1
Q8IXW0	Lamin tail domain-containing protein 2	LMNTD2 C11orf35	Homo sapiens (human)	1	1
Q8IXW5	Putative RNA polymerase II subunit B1 CTD phosphatase RPAP2	RPAP2 C1orf82	Homo sapiens (human)	4	2
Q8IXZ2	Zinc finger CCCH domain-containing protein 3	ZC3H3 KIAA0150 SMICL ZC3HDC3	Homo sapiens (human)	3	1
Q8IXZ3	Transcription factor Sp8	SP8	Homo sapiens (human)	0	1
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
Q8IY18	Structural maintenance of chromosomes protein 5	SMC5 KIAA0594 SMC5L1	Homo sapiens (human)	1	2
Q8IY21	Probable ATP-dependent RNA helicase DDX60	DDX60	Homo sapiens (human)	0	1
Q8IY22	C-Maf-inducing protein	CMIP KIAA1694 TCMIP	Homo sapiens (human)	1	1
Q8IY33	MICAL-like protein 2	MICALL2 JRAB	Homo sapiens (human)	14	2
Q8IY34	Solute carrier family 15 member 3	SLC15A3 OCTP PHT2 PTR3	Homo sapiens (human)	6	0
Q8IY37	Probable ATP-dependent RNA helicase DHX37	DHX37 DDX37 KIAA1517	Homo sapiens (human)	1	1
Q8IY42	Uncharacterized protein C4orf19	C4orf19	Homo sapiens (human)	1	1
Q8IY47	Kelch repeat and BTB domain-containing protein 2	KBTBD2 BKLHD1 KIAA1489	Homo sapiens (human)	1	1
Q8IY51	Tigger transposable element-derived protein 4	TIGD4	Homo sapiens (human)	1	1
Q8IY57	YY1-associated factor 2	YAF2	Homo sapiens (human)	2	1
Q8IY67	Ribonucleoprotein PTB-binding 1	RAVER1 KIAA1978	Homo sapiens (human)	0	1
Q8IY81	pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ3	FTSJ3	Homo sapiens (human)	2	1
Q8IY82	Dynein regulatory complex subunit 7	DRC7 C16orf50 CCDC135	Homo sapiens (human)	0	1
Q8IY84	Serine/threonine-protein kinase NIM1	NIM1K NIM1	Homo sapiens (human)	0	1

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