MGP Database

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MGP001405

Ontology/Pathway Information

Entrez Gene ID3028
Gene Namehydroxysteroid (17-beta) dehydrogenase 10
Gene Symbol HSD17B10
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005737 TAS:ProtIncCcytoplasm
GO:0005783 IEA:EnsemblCendoplasmic reticulum
GO:0005743 IEA:EnsemblCmitochondrial inner membrane
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 ISS:UniProtKBCmitochondrion
GO:0005886 TAS:ProtIncCplasma membrane
GO:0047015 IEA:UniProtKB-ECF3-hydroxy-2-methylbutyryl-CoA dehydrogenase activity
GO:0003857 EXP:ReactomeF3-hydroxyacyl-CoA dehydrogenase activity
GO:0008709 TAS:ProtIncFcholate 7-alpha-dehydrogenase activity
GO:0044822 IDA:UniProtKBFpoly(A) RNA binding
GO:0030283 IEA:UniProtKB-ECFtestosterone dehydrogenase [NAD(P)] activity
GO:0009083 TAS:ReactomePbranched-chain amino acid catabolic process
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0006629 TAS:ProtIncPlipid metabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0008033 IEA:UniProtKB-KWPtRNA processing
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_197Branched-chain amino acid catabolism
REACT_111217Metabolism
REACT_13Metabolism of amino acids and derivatives
SMP Pathway Links
SMP IDDescription
SMP001372-Methyl-3-Hydroxybutryl CoA Dehydrogenase Deficiency
SMP001383-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
SMP005213-hydroxyisobutyric acid dehydrogenase deficiency
SMP005223-hydroxyisobutyric aciduria
SMP002373-Methylcrotonyl Coa Carboxylase Deficiency Type I
SMP001393-Methylglutaconic Aciduria Type I
SMP001403-Methylglutaconic Aciduria Type III
SMP001413-Methylglutaconic Aciduria Type IV
SMP00173Beta-Ketothiolase Deficiency
SMP00054Fatty Acid Elongation In Mitochondria
SMP00523Isobutyryl-coa dehydrogenase deficiency
SMP00524Isovaleric acidemia
SMP00238Isovaleric Aciduria
SMP00544Long-chain-3-hydroxyacyl-coa dehydrogenase deficiency (LCHAD)
SMP00199Maple Syrup Urine Disease
SMP00384Methylmalonate Semialdehyde Dehydrogenase Deficiency
SMP00200Methylmalonic Aciduria
SMP00480Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids
SMP00236Propionic Acidemia
SMP00568Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (SCHAD)
SMP00032Valine, Leucine and Isoleucine Degradation
SMP00635Valproic Acid Metabolism Pathway
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