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
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Displaying entries **9626 - 9650** 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
Q9H6K4	Optic atrophy 3 protein	OPA3	Homo sapiens (human)	1	1
Q9H6K1	Protein ILRUN	ILRUN C6orf106	Homo sapiens (human)	2	1
Q9H6H4	Receptor expression-enhancing protein 4	REEP4 C8orf20	Homo sapiens (human)	1	1
Q9H6F5	Coiled-coil domain-containing protein 86	CCDC86 CYCLON	Homo sapiens (human)	0	1
Q9H6E4	Coiled-coil domain-containing protein 134	CCDC134	Homo sapiens (human)	6	2
Q9H6D8	Fibronectin type III domain-containing protein 4	FNDC4 FRCP1	Homo sapiens (human)	3	1
Q9H6B4	CXADR-like membrane protein	CLMP ACAM ASAM	Homo sapiens (human)	2	4
Q9H6B1	Zinc finger protein 385D	ZNF385D ZNF659	Homo sapiens (human)	1	1
Q9H6A9	Pecanex-like protein 3	PCNX3 PCNXL3	Homo sapiens (human)	2	0
Q9H694	Protein bicaudal C homolog 1	BICC1	Homo sapiens (human)	2	1
Q9H693	Uncharacterized protein C16orf95	C16orf95	Homo sapiens (human)	1	1
Q9H609	Zinc finger protein 576	ZNF576	Homo sapiens (human)	0	1
Q9H5Z1	Probable ATP-dependent RNA helicase DHX35	DHX35 C20orf15 DDX35	Homo sapiens (human)	1	2
Q9H5Y7	SLIT and NTRK-like protein 6	SLITRK6	Homo sapiens (human)	4	1
Q9H5V9	STING ER exit protein	STEEP1 CXorf56	Homo sapiens (human)	0	1
Q9H5V8	CUB domain-containing protein 1	CDCP1 TRASK	Homo sapiens (human)	11	39
Q9H5Q4	Dimethyladenosine transferase 2, mitochondrial	TFB2M NS5ATP5	Homo sapiens (human)	0	1
Q9H5P4	PDZ domain-containing protein 7	PDZD7 PDZK7	Homo sapiens (human)	1	1
Q9H5N1	Rab GTPase-binding effector protein 2	RABEP2 RABPT5B	Homo sapiens (human)	0	1
Q9H5L6	DNA transposase THAP9	THAP9	Homo sapiens (human)	0	1
Q9H5K3	Protein O-mannose kinase	POMK SGK196	Homo sapiens (human)	5	9	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia 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 bilateral optic nerve hypoplasia blindness cardiomyopathy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopia 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
Q9H5J4	Very long chain fatty acid elongase 6	ELOVL6 FACE LCE	Homo sapiens (human)	2	2	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
Q9H5I5	Piezo-type mechanosensitive ion channel component 2	PIEZO2 C18orf30 C18orf58 FAM38B	Homo sapiens (human)	7	4
Q9H5I1	Histone-lysine N-methyltransferase SUV39H2	SUV39H2 KMT1B	Homo sapiens (human)	0	1
Q9H598	Vesicular inhibitory amino acid transporter	SLC32A1 VGAT VIAAT	Homo sapiens (human)	1	1

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