GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **10076 - 10100** of **10109** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
64064	3-oxoacid CoA-transferase 2	OXCT2 FKSG25 FLJ00030 SCOT-T
5019	3-oxoacid CoA-transferase 1	OXCT1 SCOT Succinyl-CoA:3-ketoacid-CoA transferase
2531	3-ketodihydrosphingosine reductase	KDSR 3-dehydrosphinganine reductase DHSR SDR35C1 short chain dehydrogenase/reductase family 35C, member 1	erythrokeratodermia variabilis et progressiva 4 follicular lymphoma
26275	3-hydroxyisobutyryl-CoA hydrolase	HIBCH	3-hydroxyisobutryl-CoA hydrolase deficiency
11112	3-hydroxyisobutyrate dehydrogenase	HIBADH
56898	3-hydroxybutyrate dehydrogenase 2	BDH2 FLJ13261 PRO20933 SDR15C1 UCPA-OR UNQ6308 short chain dehydrogenase/reductase family 15C, member 1
622	3-hydroxybutyrate dehydrogenase 1	BDH1 SDR9C1 short chain dehydrogenase/reductase family 9C, member 1
401494	3-hydroxyacyl-CoA dehydratase 4	HACD4 Em:AL662879.1 OTTHUMG00000021016 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4
51495	3-hydroxyacyl-CoA dehydratase 3	HACD3 B-ind1 HSPC121 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 3
201562	3-hydroxyacyl-CoA dehydratase 2	HACD2 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2
9200	3-hydroxyacyl-CoA dehydratase 1	HACD1 CAP Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1 cementum attachment protein	congenital myopathy
3158	3-hydroxy-3-methylglutaryl-CoA synthase 2	HMGCS2	HMG-CoA synthase 2 deficiency
3157	3-hydroxy-3-methylglutaryl-CoA synthase 1	HMGCS1 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase
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
54511	3-hydroxy-3-methylglutaryl-CoA lyase like 1	HMGCLL1 DKFZP434G1411 bA418P12.1
3155	3-hydroxy-3-methylglutaryl-CoA lyase	HMGCL HL hydroxymethylglutaricaciduria hydroxymethylglutaryl-CoA lyase	3-hydroxy-3-methylglutaryl-CoA lyase deficiency amino acid metabolic disorder
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
9061	3'-phosphoadenosine 5'-phosphosulfate synthase 1	PAPSS1 ATPSK1 PAPSS adenylyl-sulfate kinase sulfate adenylyltransferase
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
10380	3'(2'), 5'-bisphosphate nucleotidase 1	BPNT1
1718	24-dehydrocholesterol reductase	DHCR24 Delta(24)-sterol reductase KIAA0018 seladin-1	lipid metabolism disorder
92370	2-phosphoxylose phosphatase 1	PXYLP1 FLJ23751
79701	2-oxoglutarate and iron dependent oxygenase domain containing 3	OGFOD3
26061	2-hydroxyacyl-CoA lyase 1	HACL1
26063	2,4-dienoyl-CoA reductase 2	DECR2

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