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
2632	1,4-alpha-glucan branching enzyme 1	GBE1 Andersen disease glycogen branching enzyme glycogen storage disease type IV	glycogen storage disease IV pulmonary tuberculosis
10554	1-acylglycerol-3-phosphate O-acyltransferase 1	AGPAT1 1-acyl-sn-glycerol-3-phosphate acyltransferase alpha LPAAT-alpha LPLAT1 lysophosphatidic acid acyltransferase, alpha lysophospholipid acyltransferase l
10555	1-acylglycerol-3-phosphate O-acyltransferase 2	AGPAT2 1-acyl-sn-glycerol-3-phosphate acyltransferase beta LPAAT-beta LPLAT2 lysophosphatidic acid acyltransferase-beta lysophospholipid acyltransferase 2	congenital generalized lipodystrophy type 1 lipodystrophy
56894	1-acylglycerol-3-phosphate O-acyltransferase 3	AGPAT3 1-acyl-sn-glycerol-3-phosphate acyltransferase gamma LPAAT-gamma LPAAT3 LPLAT3 lysophosphatidic acid acyltransferase gamma lysophospholipid acyltransferase 3
56895	1-acylglycerol-3-phosphate O-acyltransferase 4	AGPAT4 1-acyl-sn-glycerol-3-phosphate acyltransferase delta LPAAT-delta LPAAT4 LPLAT4 dJ473J16.2 lysophosphatidic acid acyltransferase, delta lysophospholipid acyltransferase 4
55326	1-acylglycerol-3-phosphate O-acyltransferase 5	AGPAT5 1-acyl-sn-glycerol-3-phosphate acyltransferase epsilon FLJ11210 LPAAT-e LPAAT-epsilon LPLAT5 lysophosphatidic acid acyltransferase, epsilon lysophospholipid acyltransferase 5
4938	2'-5'-oligoadenylate synthetase 1	OAS1	primary immunodeficiency disease
4940	2'-5'-oligoadenylate synthetase 3	OAS3
10591	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	DNPH1 dJ330M21.3 rcl
26063	2,4-dienoyl-CoA reductase 2	DECR2
26061	2-hydroxyacyl-CoA lyase 1	HACL1
79701	2-oxoglutarate and iron dependent oxygenase domain containing 3	OGFOD3
92370	2-phosphoxylose phosphatase 1	PXYLP1 FLJ23751
1718	24-dehydrocholesterol reductase	DHCR24 Delta(24)-sterol reductase KIAA0018 seladin-1	lipid metabolism disorder
10380	3'(2'), 5'-bisphosphate nucleotidase 1	BPNT1
54928	3'(2'), 5'-bisphosphate nucleotidase 2	BPNT2 FLJ20421 Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase IMPA3 gPAPP golgi-resident nucleotide phosphatase	chondrodysplasia with joint dislocations gPAPP type
9061	3'-phosphoadenosine 5'-phosphosulfate synthase 1	PAPSS1 ATPSK1 PAPSS adenylyl-sulfate kinase sulfate adenylyltransferase
9060	3'-phosphoadenosine 5'-phosphosulfate synthase 2	PAPSS2 ATPSK2 PAPS synthase 2 adenosine 5'-phosphosulfate kinase bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2	spondyloepimetaphyseal dysplasia, Pakistani type
3155	3-hydroxy-3-methylglutaryl-CoA lyase	HMGCL HL hydroxymethylglutaricaciduria hydroxymethylglutaryl-CoA lyase	3-hydroxy-3-methylglutaryl-CoA lyase deficiency amino acid metabolic disorder
54511	3-hydroxy-3-methylglutaryl-CoA lyase like 1	HMGCLL1 DKFZP434G1411 bA418P12.1
3156	3-hydroxy-3-methylglutaryl-CoA reductase	HMGCR	Alzheimer's disease Parkinson's disease asthma attention deficit hyperactivity disorder autosomal recessive limb-girdle muscular dystrophy coronary artery disease dementia diabetes mellitus intermediate coronary syndrome muscular disease type 2 diabetes mellitus
3157	3-hydroxy-3-methylglutaryl-CoA synthase 1	HMGCS1 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase
3158	3-hydroxy-3-methylglutaryl-CoA synthase 2	HMGCS2	HMG-CoA synthase 2 deficiency
9200	3-hydroxyacyl-CoA dehydratase 1	HACD1 CAP Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1 cementum attachment protein	congenital myopathy
201562	3-hydroxyacyl-CoA dehydratase 2	HACD2 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2

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