GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5451 - 5475** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
26123	tectonic family member 3	TCTN3
26130	GTPase activating protein and VPS9 domains 1	GAPVD1
26135	SERPINE1 mRNA binding protein 1	SERBP1
26137	zinc finger and BTB domain containing 20	ZBTB20
26140	tubulin tyrosine ligase like 3	TTLL3
26145	interferon regulatory factor 2 binding protein 1	IRF2BP1
26146	TRAF3 interacting protein 1	TRAF3IP1
26154	ATP binding cassette subfamily A member 12	ABCA12
26155	NOC2 like nucleolar associated transcriptional repressor	NOC2L
26156	ribosomal L1 domain containing 1	RSL1D1
26167	protocadherin beta 5	PCDHB5
26173	integrator complex subunit 1	INTS1
26189	olfactory receptor family 1 subfamily A member 2	OR1A2
26205	glucocorticoid modulatory element binding protein 2	GMEB2
26211	olfactory receptor family 2 subfamily F member 1	OR2F1
26212	olfactory receptor family 2 subfamily B member 6	OR2B6
26219	olfactory receptor family 1 subfamily J member 4	OR1J4
26227	phosphoglycerate dehydrogenase	PHGDH
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
26230	TIAM Rac1 associated GEF 2	TIAM2
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
26233	F-box and leucine rich repeat protein 6	FBXL6
26235	F-box and leucine rich repeat protein 4	FBXL4
26245	olfactory receptor family 2 subfamily M member 4	OR2M4
26246	olfactory receptor family 2 subfamily L member 2	OR2L2

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