GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **9476 - 9500** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
346157	zinc finger protein 391	ZNF391
346517	olfactory receptor family 6 subfamily V member 1	OR6V1
346525	olfactory receptor family 2 subfamily A member 12	OR2A12
346528	olfactory receptor family 2 subfamily A member 1	OR2A1
346562	G protein subunit alpha transducin 3	GNAT3
346606	monoacylglycerol O-acyltransferase 3	MOGAT3 DC7 DGAT2L2 MGAT3	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 Pick's disease Reye syndrome cerebral degeneration steatotic liver disease
346673	stimulated by retinoic acid 8	STRA8
346689	killer cell lectin like receptor G2	KLRG2 C-type lectin domain family 15, member B CLEC15B FLJ44186	prostate cancer prostate carcinoma
347051	solute carrier family 10 member 5	SLC10A5
347168	olfactory receptor family 1 subfamily J member 1	OR1J1
347169	olfactory receptor family 1 subfamily B member 1	OR1B1
347252	insulin like growth factor binding protein like 1	IGFBPL1
347365	inter-alpha-trypsin inhibitor heavy chain family member 6	ITIH6
347404	LanC like family member 3	LANCL3
347468	olfactory receptor family 13 subfamily H member 1	OR13H1
347487	chromosome X open reading frame 66	CXorf66
347516	diacylglycerol O-acyltransferase 2 like 6	DGAT2L6
347527	arylsulfatase family member H	ARSH	Marfan syndrome Richter's syndrome X-linked chondrodysplasia punctata 1 acquired immunodeficiency syndrome acrodermatitis alcoholic liver cirrhosis autosomal dominant chondrodysplasia punctata cancer childhood leukemia chondrodysplasia punctata chronic lymphocytic leukemia dermatitis dyschromatosis symmetrica hereditaria essential thrombocythemia gallbladder disease hepatitis human immunodeficiency virus infectious disease leukemia liver cirrhosis liver disease microphthalmia mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis myelodysplastic syndrome neuroblastoma obsolete Matthew-Wood syndrome oculocerebrorenal syndrome rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 situs inversus tuberous sclerosis ventricular septal defect
347730	leucine rich repeat transmembrane neuronal 1	LRRTM1
347731	leucine rich repeat transmembrane neuronal 3	LRRTM3
347733	tubulin beta 2B class IIb	TUBB2B
347734	solute carrier family 35 member B2	SLC35B2 UGTrel4	B-cell lymphoma Hodgkin's granuloma Hodgkin's lymphoma, mixed cellularity Langerhans cell sarcoma Langerhans-cell histiocytosis Richter's syndrome adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer central nervous system lymphoma childhood lymphoma chronic lymphocytic leukemia/small lymphocytic lymphoma chronic lymphocytic leukemia dendritic cell sarcoma dilated cardiomyopathy 1A dilated cardiomyopathy follicular dendritic cell sarcoma follicular lymphoma hereditary multiple exostoses hypomyelinating leukodystrophy 26 interdigitating dendritic cell sarcoma invasive ductal carcinoma lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia mantle cell lymphoma non-Hodgkin lymphoma obesity obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma reticulosarcoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood
347862	glutamine amidotransferase class 1 domain containing 1	GATD1
347902	adhesion molecule with Ig like domain 2	AMIGO2
348158	acyl-CoA synthetase medium chain family member 2B	ACSM2B HXMA HYST1046 xenobiotic/medium chain fatty acid:CoA ligase

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