Hsd17b4 - hydroxysteroid (17-beta) dehydrogenase 4 Gene
Also Known as DBP; MFP2; MFE-2; MPF-2; Mfp-2; perMFE-2; 17[b]-HSD; 17-beta-HSD
Species: Mus musculus
Summary
Predicted to enable hydro-lyase activity; oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor; and protein homodimerization activity. Acts upstream of or within Sertoli cell development; fatty acid beta-oxidation; and very long-chain fatty acid metabolic process. Located in peroxisome. Is expressed in several structures, including brain; genitourinary system; hindlimb phalanx; integumental system; and jaw. Used to study D-bifunctional protein deficiency. Human ortholog(s) of this gene implicated in D-bifunctional protein deficiency; Perrault syndrome; and Stiff-Person syndrome. Orthologous to human HSD17B4 (hydroxysteroid 17-beta dehydrogenase 4). [provided by Alliance of Genome Resources, Apr 2022]
Hsd17b4 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_008292.4 | NP_032318.2 | peroxisomal multifunctional enzyme type 2 |
| Molecular Function GO Annotation | Evidence | Referencias | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32814053 | MGI |
| Biological Process GO Annotation | Evidence | Referencias | Source |
|---|---|---|---|
| acts upstream of or within Sertoli cell development |
IMP
IMP: Inferred from mutant phenotype
|
16484321 | MGI |
| acts upstream of or within fatty acid beta-oxidation |
IMP
IMP: Inferred from mutant phenotype
|
17442273 | MGI |
| acts upstream of or within very long-chain fatty acid metabolic process |
IMP
IMP: Inferred from mutant phenotype
|
16484321 | MGI |
| Cellular Component GO Annotation | Evidence | Referencias | Source |
|---|---|---|---|
| located in peroxisome |
IDA
IDA: Inferred from direct assay
|
12897163 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
peroxisomal multifunctional enzyme type 2 |
|
|