GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **4501 - 4525** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
26290	polypeptide N-acetylgalactosaminyltransferase 8	GALNT8 GALNAC-T8 polypeptide GalNAc transferase 8	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C
26286	ARF GTPase activating protein 3	ARFGAP3
26280	interleukin 1 receptor accessory protein like 2	IL1RAPL2 IL-1R9 IL1R9 IL1RAPL-2 TIGIRR-1	autism spectrum disorder autistic disorder breast cancer childhood type dermatomyositis dermatomyositis hepatitis C myositis
26279	phospholipase A2 group IID	PLA2G2D sPLA2S	Down syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascending cholangitis atherosclerosis breast cancer cancer cholangitis chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease embryoma large intestine cancer primary sclerosing cholangitis sclerosing cholangitis suppurative cholangitis
26278	sacsin molecular chaperone	SACS
26276	VPS33B late endosome and lysosome associated	VPS33B
26275	3-hydroxyisobutyryl-CoA hydrolase	HIBCH	Leigh disease Unverricht-Lundborg syndrome West syndrome agnosia arthritis arthropathy blepharospasm brain disease cancer colorectal cancer colorectal carcinoma congenital nystagmus cryptorchidism developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy epilepsy focal hand dystonia generalized dystonia hydrocephalus hypertropia inherited metabolic disorder lactic acidosis large intestine cancer mechanical strabismus neurodegenerative disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus spontaneous ocular nystagmus strabismus tetralogy of Fallot visual epilepsy
26271	F-box protein 5	FBXO5
26262	tetraspanin 17	TSPAN17
26256	calcium binding tyrosine phosphorylation regulated	CABYR
26254	opticin	OPTC
26253	C-type lectin domain family 4 member E	CLEC4E MINCLE Macrophage-inducible C-type lectin	acute myocardial infarction allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis coronary thrombosis depressive disorder dysthymic disorder intrinsic asthma keratitis keratoconjunctivitis major depressive disorder melancholic depression multiple sclerosis mycotic corneal ulcer myocardial infarction neurotic disorder obsolete melancholia pulmonary tuberculosis rheumatoid arthritis silent myocardial infarction tuberculosis tuberculous pneumothorax
26248	olfactory receptor family 2 subfamily K member 2	OR2K2
26246	olfactory receptor family 2 subfamily L member 2	OR2L2
26245	olfactory receptor family 2 subfamily M member 4	OR2M4
26235	F-box and leucine rich repeat protein 4	FBXL4
26233	F-box and leucine rich repeat protein 6	FBXL6
26232	F-box protein 2	FBXO2 FBX2 Fbg1 Fbs1 Nfb42	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome cerebral degeneration hyperglycemia rheumatoid arthritis stomach cancer stomach carcinoma
26230	TIAM Rac1 associated GEF 2	TIAM2
26229	beta-1,3-glucuronyltransferase 3	B3GAT3 GlcAT-I galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 glucuronosyltransferase I	Hailey-Hailey disease Laron syndrome Larsen-like syndrome B3GAT3 type Marfan syndrome Rothmund-Thomson syndrome achondroplasia amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease buphthalmos cancer cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital heart disease craniosynostosis cutis laxa esotropia geroderma osteodysplasticum glaucoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hydrophthalmos hyperopia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis isolated cleft palate juvenile glaucoma liver cancer liver carcinoma mal de Meleda mitral valve insufficiency mitral valve prolapse monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia obstructive hydrocephalus osteochondrodysplasia osteoporosis patent foramen ovale postinflammatory pulmonary fibrosis postural orthostatic tachycardia syndrome pulmonary fibrosis radioulnar synostosis refractive error restrictive dermopathy scoliosis senile degeneration of brain situs inversus strabismic amblyopia thoracic aortic aneurysm tuberous sclerosis
26227	phosphoglycerate dehydrogenase	PHGDH
26219	olfactory receptor family 1 subfamily J member 4	OR1J4
26212	olfactory receptor family 2 subfamily B member 6	OR2B6
26211	olfactory receptor family 2 subfamily F member 1	OR2F1
26205	glucocorticoid modulatory element binding protein 2	GMEB2

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