Mus musculus Gene: Hsd17b10
Summary
InnateDB Gene IDBG-179843.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Hsd17b10
Gene Name hydroxysteroid (17-beta) dehydrogenase 10
Synonyms 17bHSD10; Ads9; ERAB; Hadh2
Species Mus musculus
Ensembl Gene ENSMUSG00000025260
Encoded Proteins
hydroxysteroid (17-beta) dehydrogenase 10
hydroxysteroid (17-beta) dehydrogenase 10
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000072506:
This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids, alcohols, and steroids. The protein has been implicated in the development of Alzheimer's disease, and mutations in the gene are the cause of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBD). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008]
This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids and steroids, and is a subunit of mitochondrial ribonuclease P, which is involved in tRNA maturation. The protein has been implicated in the development of Alzheimer disease, and mutations in the gene are the cause of 17beta-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency. Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Aug 2014]
Gene Information
Type Protein coding
Genomic Location Chromosome X:152001845-152004442
Strand Forward strand
Band F3
Transcripts
ENSMUST00000026289 ENSMUSP00000026289
ENSMUST00000112617 ENSMUSP00000108236
ENSMUST00000151200
ENSMUST00000140804
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 20 interaction(s) predicted by orthology.
Predicted by orthology
Total 20 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003857 3-hydroxyacyl-CoA dehydrogenase activity
GO:0005515 protein binding
GO:0016491 oxidoreductase activity
GO:0044822 poly(A) RNA binding
Biological Process
GO:0008152 metabolic process
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0005783 endoplasmic reticulum
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
KEGG
Valine, leucine and isoleucine degradation pathway
Alzheimer's disease pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Branched-chain amino acid catabolism pathway
Metabolism of amino acids and derivatives pathway
Metabolism pathway
Metabolism of amino acids and derivatives pathway
Branched-chain amino acid catabolism pathway
Metabolism pathway
KEGG
Valine, leucine and isoleucine degradation pathway
Alzheimer's disease pathway
INOH
Tryptophan degradation pathway
Butanoate metabolism pathway
Valine Leucine Isoleucine degradation pathway
PID NCI
Cross-References
SwissProt
TrEMBL A2AFQ2 Q99N15
UniProt Splice Variant
Entrez Gene 15108
UniGene Mm.400760
RefSeq NM_016763
OMIM
CCDS CCDS30471
HPRD
IMGT
MGI ID MGI:1333871
MGI Symbol Hsd17b10
EMBL AF233685 AK077735 AK088685 AL672180 BC027517
GenPept AAH27517 AAK15008 BAC36987 BAC40505
RNA Seq Atlas 15108