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 **16201 - 16225** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
O14646	Chromodomain-helicase-DNA-binding protein 1	CHD1	Homo sapiens (human)	1	2
Q9BRQ6	MICOS complex subunit MIC25	CHCHD6 CHCM1 MIC25	Homo sapiens (human)	0	1
Q8N4Q1	Mitochondrial intermembrane space import and assembly protein 40	CHCHD4 MIA40	Homo sapiens (human)	0	1
Q9NX63	MICOS complex subunit MIC19	CHCHD3 MIC19 MINOS3	Homo sapiens (human)	1	1
Q5T1J5	Putative coiled-coil-helix-coiled-coil-helix domain-containing protein CHCHD2P9, mitochondrial	CHCHD2P9 C9orf49 CHCHD9	Homo sapiens (human)	3	1
Q96BP2	Small ribosomal subunit protein mS37	CHCHD1 C10orf34 MRPS37	Homo sapiens (human)	0	1
P28329	Choline O-acetyltransferase	CHAT	Homo sapiens (human)	3	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balo concentric sclerosis Down syndrome Gilles de la Tourette syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lambert-Eaton myasthenic syndrome Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Rett syndrome Reye syndrome X-linked adrenal hypoplasia congenita acute myocardial infarction adrenoleukodystrophy agnosia allergic asthma amnestic disorder amyloidosis angle-closure glaucoma arthritis arthropathy aspiration pneumonia aspiration pneumonitis asthma atrial fibrillation autism spectrum disorder autistic disorder beriberi bronchus cancer bronchus carcinoma bulbar polio cancer cannabis abuse cannabis dependence central nervous system disease central sleep apnea centronuclear myopathy cerebral degeneration cerebral infarction cerebrovascular disease chronic closed-angle glaucoma chronic fatigue syndrome clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital myasthenic syndrome 21 congenital myasthenic syndrome 6 congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy coronary thrombosis critical illness polyneuropathy dementia depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis differentiating neuroblastoma disease of mental health dissociated nystagmus dry beriberi dysthymic disorder encephalitis encephalomyelitis epilepsy esophagitis esotropia focal epilepsy gastroesophageal reflux disease gastroparesis giant cell glioblastoma glioblastoma hypertropia hypoglycemia idiopathic interstitial pneumonia intellectual disability intrinsic asthma kernicterus due to isoimmunization kernicterus lactic acidosis large intestine cancer learning disability lung benign neoplasm lung cancer lung carcinoma lymphocytic choriomeningitis major depressive disorder mechanical strabismus melancholic depression middle cerebral artery infarction monocular esotropia mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple sclerosis myelitis myocardial infarction narcolepsy nervous system disease neuroblastoma neurodegenerative disease neuromuscular disease neurotic disorder nicotine dependence obsolete constipation obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea olivopontocerebellar atrophy ophthalmoplegia osteoarthritis partial motor epilepsy pathologic nystagmus pellagra peptic esophagitis poliomyelitis polyhydramnios polyneuropathy postinflammatory pulmonary fibrosis primary angle-closure glaucoma progressive bulbar palsy psychotic disorder ptosis pulmonary fibrosis red-green color blindness retinal disease retinitis retrograde amnesia rheumatoid arthritis schizophrenia scoliosis secondary Parkinson disease sensorineural hearing loss silent myocardial infarction situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus sudden infant death syndrome tendinitis thiamine deficiency disease tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus vascular dementia visual epilepsy
Q96JM3	Chromosome alignment-maintaining phosphoprotein 1	CHAMP1 C13orf8 CAMP CHAMP KIAA1802 ZNF828	Homo sapiens (human)	8	2
Q13112	Chromatin assembly factor 1 subunit B	CHAF1B CAF1A CAF1P60 MPHOSPH7 MPP7	Homo sapiens (human)	0	1
Q13111	Chromatin assembly factor 1 subunit A	CHAF1A CAF CAF1P150	Homo sapiens (human)	1	2
Q6NUI6	Chondroadherin-like protein	CHADL SLRR4B	Homo sapiens (human)	2	0
O15335	Chondroadherin	CHAD SLRR4A	Homo sapiens (human)	1	0
Q8WUX2	Glutathione-specific gamma-glutamylcyclotransferase 2	CHAC2	Homo sapiens (human)	0	1
O95992	Cholesterol 25-hydroxylase	CH25H	Homo sapiens (human)	3	0	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balo concentric sclerosis Marfan syndrome Pick's disease Reye syndrome Zika fever adrenoleukodystrophy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis bacterial infectious disease central nervous system disease cerebral degeneration childhood leukemia chronic fatigue syndrome chronic obstructive pulmonary disease colitis coronary artery disease encephalitis encephalomyelitis familial hypercholesterolemia gastroenteritis giant cell glioblastoma glioblastoma hepatitis C high grade glioma ileitis ileocolitis leukemia melanoma microcephaly multiple sclerosis myelitis narcolepsy nervous system disease neuromyelitis optica osteoarthritis plasmacytoma polycythemia vera polycythemia pulmonary emphysema rabies situs inversus skin melanoma tuberous sclerosis type 2 diabetes mellitus
Q99674	Cell growth regulator with EF hand domain protein 1	CGREF1 CGR11	Homo sapiens (human)	9	3
Q0VF96	Cingulin-like protein 1	CGNL1 JACOP KIAA1749	Homo sapiens (human)	1	4
Q9UFW8	CGG triplet repeat-binding protein 1	CGGBP1 CGGBP	Homo sapiens (human)	0	1
P0DN87	Choriogonadotropin subunit beta 7	CGB7	Homo sapiens (human)	6	0
A0A0F7RQF0	Chorionic gonadotropin beta subunit 5	CGB5	Homo sapiens (human)	1	0
P0DN86	Choriogonadotropin subunit beta 3	CGB3 CGB5 CGB8 CGB	Homo sapiens (human)	8	43
A0A0F7RQP8	Chorionic gonadotropin beta subunit 3	CGB3 CGB4	Homo sapiens (human)	1	0
A0A0F7RPU2	Chorionic gonadotropin beta subunit 2	CGB2	Homo sapiens (human)	1	0
M0R0E6	Chorionic gonadotropin subunit beta 2 (Fragment)	CGB2	Homo sapiens (human)	1	0
Q6NT52	Choriogonadotropin subunit beta variant 2	CGB2	Homo sapiens (human)	2	0
A6NKQ9	Choriogonadotropin subunit beta variant 1	CGB1	Homo sapiens (human)	2	1

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