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HSD17B10

HSD17B10

Protein-coding gene in the species Homo sapiens

dehydrogenase type-2 is a mitochondrial enzyme that in humans is encoded by the HSD17B10 (hydroxysteroid (17β) dehydrogenase 10) gene. Several alternatively spliced

HSD17B10

17β-Hydroxysteroid dehydrogenase

Class of enzymes

retinoid metabolism. Mutations are associated with fundus albipunctatus. HSD17B10: Also known as 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD). Substrates

17β-Hydroxysteroid dehydrogenase

17β-Hydroxysteroid_dehydrogenase

Short-chain dehydrogenase

Protein family

DHRS8; DHRS9; DHRSX; FASN; FVT1; HADH2; HPGD; HSD11B1; HSD11B2; HSD17B1; HSD17B10; HSD17B12; HSD17B13; HSD17B2; HSD17B3; HSD17B4; HSD17B6; HSD17B7; HSD17B7P2;

Short-chain dehydrogenase

Short-chain_dehydrogenase

3-hydroxyacyl-CoA dehydrogenase

Enzyme

3-hydroxyacyl-CoA dehydrogenase activity: HADH – Hydroxyacyl-Coenzyme A dehydrogenase HSD17B10 – 3-Hydroxyacyl-CoA dehydrogenase type-2 EHHADH – Peroxisomal bifunctional

3-hydroxyacyl-CoA dehydrogenase

3-hydroxyacyl-CoA_dehydrogenase

Amyloid-beta precursor protein

Mammalian protein found in humans

APBB1, APPBP1, APPBP2, BCAP31, BLMH CLSTN1, CAV1, COL25A1, Fibulin-1, GSN, HSD17B10, and SHC-transforming protein 1. APP interacts with reelin, a protein implicated

Amyloid-beta precursor protein

Amyloid-beta_precursor_protein

Androgen backdoor pathway

Series of interconnected biochemical reactions

that has 3α-hydroxysteroid oxidase activity, such as AKR1C2, HSD17B6, HSD17B10, RDH16, RDH5, and DHRS9. This oxidation is not required in the classical

Androgen backdoor pathway

Androgen_backdoor_pathway

Ribonuclease P

Class of enzymes

is a trimeric protein and does not contain RNA. It consists of TRMT10C, HSD17B10, and the catalytic PRORP. Its structure has been solved. The PPR domain

Ribonuclease P

Ribonuclease_P

List of OMIM disorder codes

202110; CYP17A1 17-beta-hydroxysteroid dehydrogenase X deficiency; 300438; HSD17B10 2-methylbutyrylglycinuria; 610006; ACADSB 3-hydroxyacyl-coa dehydrogenase

List of OMIM disorder codes

List_of_OMIM_disorder_codes

List of human protein-coding genes 4

HGNC:23316; O14756 7292 HSD17B7 HGNC:5215; P56937 7293 HSD17B8 HGNC:3554 7294 HSD17B10 HGNC:4800; Q99714 7295 HSD17B11 HGNC:22960; Q8NBQ5 7296 HSD17B12 HGNC:18646;

List of human protein-coding genes 4

List_of_human_protein-coding_genes_4

Xp11.2 duplication

Genetic disorder

2008). "Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation"

Xp11.2 duplication