GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (10109) Glycans (5831) Glycoproteins (15834) Lectins (297) Pathways (2074)

Displaying entries **1 - 25** of **10109** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
1	alpha-1-B glycoprotein	A1BG
2	alpha-2-macroglobulin	A2M	Alzheimer's disease COVID-19 Parkinson's disease background diabetic retinopathy multiple sclerosis obstructive lung disease
10	N-acetyltransferase 2	NAT2	Behcet's disease Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia allergic contact dermatitis asthma atopic dermatitis cholangiocarcinoma chronic obstructive pulmonary disease diabetes mellitus laryngeal squamous cell carcinoma leukemia lung cancer lung disease malignant mesothelioma occupational dermatitis oral mucosa leukoplakia pancreatic cancer progressive supranuclear palsy prostate cancer psoriasis pulmonary tuberculosis senile cataract systemic lupus erythematosus systemic scleroderma transitional cell carcinoma urinary bladder cancer
12	serpin family A member 3	SERPINA3	chronic obstructive pulmonary disease cystic fibrosis vasculitis
13	arylacetamide deacetylase	AADAC CES5A1 DAC
16	alanyl-tRNA synthetase 1	AARS1	Charcot-Marie-Tooth disease axonal type 2N developmental and epileptic encephalopathy 29 leukodystrophy trichothiodystrophy
18	4-aminobutyrate aminotransferase	ABAT 4-aminobutyrate transaminase GABA transaminase GABA-T GABAT gamma-aminobutyrate aminotransferase	Alzheimer's disease GABA aminotransferase deficiency Huntington's disease
19	ATP binding cassette subfamily A member 1	ABCA1	Alzheimer's disease Tangier disease coronary artery disease hypolipoproteinemia obesity primary hypoalphalipoproteinemia 1 type 2 diabetes mellitus
20	ATP binding cassette subfamily A member 2	ABCA2
21	ATP binding cassette subfamily A member 3	ABCA3	pulmonary alveolar proteinosis
22	ATP binding cassette subfamily B member 7	ABCB7	X-linked sideroblastic anemia with ataxia
24	ATP binding cassette subfamily A member 4	ABCA4	age related macular degeneration 2 cone-rod dystrophy 3 fundus dystrophy macular degeneration retinal degeneration retinitis pigmentosa 19 retinitis pigmentosa
25	ABL proto-oncogene 1, non-receptor tyrosine kinase	ABL1	B-lymphoblastic leukemia/lymphoma acute myeloid leukemia chronic myeloid leukemia colorectal cancer esophagus adenocarcinoma oral squamous cell carcinoma
26	amine oxidase copper containing 1	AOC1
27	ABL proto-oncogene 2, non-receptor tyrosine kinase	ABL2
28	ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase	ABO A3GALNT A3GALT1	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
29	ABR activator of RhoGEF and GTPase	ABR
30	acetyl-CoA acyltransferase 1	ACAA1 Lnc-Myd88 peroxisomal 3-oxoacyl-Coenzyme A thiolase
31	acetyl-CoA carboxylase alpha	ACACA ACACalpha ACC-alpha ACC1 ACCA ACCalpha Acac1 acetyl-CoA carboxylase 1 hACC1
32	acetyl-CoA carboxylase beta	ACACB ACACbeta ACC-beta ACC2 ACCB ACCbeta HACC275 acetyl-CoA carboxylase 2
33	acyl-CoA dehydrogenase long chain	ACADL ACAD4 LCAD long-chain acyl-CoA dehydrogenase
34	acyl-CoA dehydrogenase medium chain	ACADM ACAD1 MCAD MCADH medium-chain acyl-CoA dehydrogenase	medium chain acyl-CoA dehydrogenase deficiency
35	acyl-CoA dehydrogenase short chain	ACADS ACAD3 SCAD	alcohol use disorder short chain acyl-CoA dehydrogenase deficiency
36	acyl-CoA dehydrogenase short/branched chain	ACADSB ACAD7 SBCAD
37	acyl-CoA dehydrogenase very long chain	ACADVL ACAD6 LCACD VLCAD	very long chain acyl-CoA dehydrogenase deficiency

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