# Hydroxysteroid 17-beta dehydrogenase 10

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21116211](https://www.wikidata.org/wiki/Q21116211)  
**Source**: https://4ort.xyz/entity/hydroxysteroid-17-beta-dehydrogenase-10-q21116211


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q99714)
3. [Swiss-Prot](http://www.uniprot.org/uniprot/Q99714.txt?version=178)
4. Q20641742
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q99714&geneProductId=UniProtKB:Q99714)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
7. [The MRPP1/MRPP2 complex is a tRNA-maturation platform in human mitochondria](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
8. [A Map of Human Mitochondrial Protein Interactions Linked to Neurodegeneration Reveals New Mechanisms of Redox Homeostasis and NF-κB Signaling](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
9. [RNase P without RNA: Identification and Functional Reconstitution of the Human Mitochondrial tRNA Processing Enzyme](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
10. [An intracellular protein that binds amyloid-β peptide and mediates neurotoxicity in Alzheimer's disease](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
11. [A subcomplex of human mitochondrial RNase P is a bifunctional methyltransferase—extensive moonlighting in mitochondrial tRNA biogenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
12. [The mRNA-Bound Proteome and Its Global Occupancy Profile on Protein-Coding Transcripts](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q99714&geneProductId=UniProtKB:Q99714)
13. [Novel patient missense mutations in the HSD17B10 gene affect dehydrogenase and mitochondrial tRNA modification functions of the encoded protein](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q99714&geneProductId=UniProtKB:Q99714)
14. [Molecular insights into HSD10 disease: impact of SDR5C1 mutations on the human mitochondrial RNase P complex](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q99714&geneProductId=UniProtKB:Q99714)
15. [A subcomplex of human mitochondrial RNase P is a bifunctional methyltransferase—extensive moonlighting in mitochondrial tRNA biogenesis](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q99714&geneProductId=UniProtKB:Q99714)
16. [2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 gene.](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q99714&geneProductId=UniProtKB:Q99714)
17. [The mRNA-Bound Proteome and Its Global Occupancy Profile on Protein-Coding Transcripts](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
18. [Novel patient missense mutations in the HSD17B10 gene affect dehydrogenase and mitochondrial tRNA modification functions of the encoded protein](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
19. [Molecular insights into HSD10 disease: impact of SDR5C1 mutations on the human mitochondrial RNase P complex](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
20. [A non‐enzymatic function of 17β‐hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
21. [Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired processing of mitochondrial heavy strand transcripts](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99714)
22. Ensembl Release 99