|Institutional Source||Beutler Lab|
|Gene Name||hydroxysteroid (17-beta) dehydrogenase 4|
|Synonyms||D-bifunctional protein, MFP2, multifunctional protein 2, 17[b]-HSD, Mfp-2, perMFE-2, MFE-2|
|Is this an essential gene?||Possibly non essential (E-score: 0.373)|
|Stock #||R2197 (G1)|
|Chromosomal Location||50128201-50196269 bp(+) (GRCm38)|
|Type of Mutation||splice site (5 bp from exon)|
|DNA Base Change (assembly)||G to A at 50183302 bp|
|Amino Acid Change|
|Ref Sequence||ENSEMBL: ENSMUSP00000025385 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000025385]|
|Predicted Effect||probably null
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]
PHENOTYPE: Mice homozygous for disruptions in this gene have abnormalities in fatty acid metabolism, retarded growth, abnormal bile salt composition, impaired coordination, demyelination and premature death. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Hsd17b4||
(F):5'- CACTTCTGGGGCATATTTCGC -3'
(R):5'- CGCCAGCACATTACTTACATGG -3'
(F):5'- CTGGGGCATATTTCGCTAATAAG -3'
(R):5'- CATTACTTACATGGAATGTAGGCAGG -3'