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Human Gene AKR1C4 (ENST00000380448.5) from GENCODE V49
  Description: Cytosolic aldo-keto reductase that catalyzes the NADH and NADPH-dependent reduction of ketosteroids to hydroxysteroids. Liver specific enzyme that acts as an NAD(P)(H)-dependent 3-, 17- and 20- ketosteroid reductase on the steroid nucleus and side chain (PubMed:14672942, PubMed:10998348, PubMed:7650035, PubMed:1530633, PubMed:11158055, PubMed:10634139, PubMed:19218247). Displays the ability to catalyze both oxidation and reduction in vitro, but most probably acts as a reductase in vivo since the oxidase activity measured in vitro is inhibited by physiological concentration of NADPH (PubMed:14672942). Acts preferentially as a 3-alpha-hydroxysteroid dehydrogenase (HSD) with a subsidiary 3-beta-HSD activity (PubMed:14672942). Catalyzes efficiently the transformation of the potent androgen 5-alpha-dihydrotestosterone (5alpha-DHT or 17beta- hydroxy-5alpha-androstan-3-one) into the less active form, 5-alpha- androstan-3-alpha,17-beta-diol (3-alpha-diol) (PubMed:11158055, PubMed:10998348, PubMed:14672942). Catalyzes the reduction of estrone into 17beta-estradiol but with low efficiency (PubMed:14672942). Metabolizes a broad spectrum of natural and synthetic therapeutic steroid and plays an important role in metabolism of androgens, estrogens, progestereone and conjugated steroids (PubMed:10998348, PubMed:14672942, PubMed:19218247). Catalyzes the biotransformation of the pesticide chlordecone (kepone) to its corresponding alcohol leading to increased biliary excretion of the pesticide and concomitant reduction of its neurotoxicity since bile is the major excretory route (PubMed:2427522). (from UniProt P17516)
Gencode Transcript: ENST00000380448.5
Gencode Gene: ENSG00000198610.12
Transcript (Including UTRs)
   Position: hg38 chr10:5,195,463-5,218,949 Size: 23,487 Total Exon Count: 11 Strand: +
Coding Region
   Position: hg38 chr10:5,196,868-5,218,760 Size: 21,893 Coding Exon Count: 9 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesMethods
Data last updated at UCSC: 2025-09-17 13:57:07

-  Comments and Description Text from UniProtKB
  ID: AK1C4_HUMAN
DESCRIPTION: RecName: Full=Aldo-keto reductase family 1 member C4; EC=1.1.1.-; AltName: Full=3-alpha-HSD1; AltName: Full=3-alpha-hydroxysteroid dehydrogenase type I; EC=1.1.1.50; AltName: Full=Chlordecone reductase; Short=CDR; EC=1.1.1.225; AltName: Full=Dihydrodiol dehydrogenase 4; Short=DD-4; Short=DD4; AltName: Full=HAKRA;
FUNCTION: Catalyzes the transformation of the potent androgen dihydrotestosterone (DHT) into the less active form, 5-alpha- androstan-3-alpha,17-beta-diol (3-alpha-diol). Also has some 20- alpha-hydroxysteroid dehydrogenase activity. The biotransformation of the pesticide chlordecone (kepone) to its corresponding alcohol leads to increased biliary excretion of the pesticide and concomitant reduction of its neurotoxicity since bile is the major excretory route.
CATALYTIC ACTIVITY: Chlordecone alcohol + NADP(+) = chlordecone + NADPH.
CATALYTIC ACTIVITY: Androsterone + NAD(P)(+) = 5-alpha-androstane- 3,17-dione + NAD(P)H.
SUBUNIT: Monomer.
SUBCELLULAR LOCATION: Cytoplasm.
TISSUE SPECIFICITY: Liver specific.
PTM: The N-terminus is blocked.
POLYMORPHISM: The allele with Cys-145/Val-311 shows a three- to five-fold decrease in catalytic efficiency for xenobiotic and steroidal substrates compared to the Ser-145/Leu-311 allele.
DISEASE: Defects in AKR1C4 are a cause of 46,XY sex reversal type 8 (SRXY8) [MIM:614279]. A disorder of sex development. Affected individuals have a 46,XY karyotype but present as phenotypically normal females. Note=AKR1C4 mutations may act as modifier of disease severity in SRXY8 patients. A splicing mutation resulting in loss of exon 2 has been found in affected individuals also carrying mutation Val-79 in AKR1C2 (PubMed:21802064).
SIMILARITY: Belongs to the aldo/keto reductase family.
SEQUENCE CAUTION: Sequence=AAA35658.1; Type=Erroneous initiation; Note=Translation N-terminally extended;

-  Primer design for this transcript
 

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-  MalaCards Disease Associations
  MalaCards Gene Search: AKR1C4
Diseases sorted by gene-association score: 46xy sex reversal 8* (424)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene
  • C076588 benzo(a)pyrene-7,8-dione
  • C019106 tetralol
  • C025205 1,10-phenanthroline
  • C055238 1-chloro-4-(2,2-dichloro-1-(4-chlorophenyl)ethenyl)-3-(methylsulfonyl)benzene
  • C016515 1-indanol
  • D004092 20-alpha-Dihydroprogesterone
  • C018156 3',3'',5',5''-tetrabromophenolphthalein
  • C016583 4-(N-methyl-N-nitrosamino)-1-(3-pyridyl)-1-butanone
  • D043582 5-alpha-Dihydroprogesterone
  • C045993 5-dihydrocortisone
          more ... click here to view the complete list

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 96.37 RPKM in Liver
Total median expression: 97.63 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
 
Expression ratio colors:

GNF Expression Atlas 2 Data from U133A and GNF1H Chips

      
      
      
     
    
     
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -42.00253-0.166 Picture PostScript Text
3' UTR -43.60189-0.231 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR001395 - Aldo/ket_red
IPR018170 - Aldo/ket_reductase_CS
IPR020471 - Aldo/keto_reductase_subgr
IPR023210 - NADP_OxRdtase_dom

Pfam Domains:
PF00248 - Aldo/keto reductase family

Protein Data Bank (PDB) 3-D Structure
MuPIT help
2FVL - X-ray MuPIT


ModBase Predicted Comparative 3D Structure on P17516
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-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
      
      
      
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0001758 retinal dehydrogenase activity
GO:0004033 aldo-keto reductase (NADP) activity
GO:0009055 electron carrier activity
GO:0015125 bile acid transmembrane transporter activity
GO:0016491 oxidoreductase activity
GO:0016655 oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor
GO:0047023 androsterone dehydrogenase activity
GO:0047743 chlordecone reductase activity

Biological Process:
GO:0001523 retinoid metabolic process
GO:0006699 bile acid biosynthetic process
GO:0008202 steroid metabolic process
GO:0008209 androgen metabolic process
GO:0015721 bile acid and bile salt transport
GO:0022900 electron transport chain
GO:0044597 daunorubicin metabolic process
GO:0044598 doxorubicin metabolic process
GO:0055114 oxidation-reduction process
GO:0071395 cellular response to jasmonic acid stimulus

Cellular Component:
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0070062 extracellular exosome


-  Descriptions from all associated GenBank mRNAs
  S68290 - chlordecone reductase homolog {clone HAKRc} [human, liver, mRNA, 1158 nt].
AK314988 - Homo sapiens cDNA, FLJ95910.
LP747419 - Sequence 6 from Patent WO2018009939.
BC020744 - Homo sapiens aldo-keto reductase family 1, member C4 (chlordecone reductase; 3-alpha hydroxysteroid dehydrogenase, type I; dihydrodiol dehydrogenase 4), mRNA (cDNA clone MGC:22581 IMAGE:4734943), complete cds.
S68287 - chlordecone reductase {clone HAKRa} [human, liver, mRNA, 1167 nt].
CU676682 - Synthetic construct Homo sapiens gateway clone IMAGE:100022237 5' read AKR1C4 mRNA.
KJ896595 - Synthetic construct Homo sapiens clone ccsbBroadEn_05989 AKR1C4 gene, encodes complete protein.
KR711253 - Synthetic construct Homo sapiens clone CCSBHm_00021501 AKR1C4 (AKR1C4) mRNA, encodes complete protein.
DQ894598 - Synthetic construct Homo sapiens clone IMAGE:100009058; FLH176796.01L; RZPDo839H06121D aldo-keto reductase family 1, member C4 (chlordecone reductase; 3-alpha hydroxysteroid dehydrogenase, type I; dihydrodiol dehy> (AKR1C4) gene, encodes complete protein.
AB031085 - Homo sapiens mRNA for dihydrodiol dehydrogenase 4, complete cds.
DQ891424 - Synthetic construct clone IMAGE:100004054; FLH176800.01X; RZPDo839H06122D aldo-keto reductase family 1, member C4 (chlordecone reductase; 3-alpha hydroxysteroid dehydrogenase, type I; dihydrodiol dehy> (AKR1C4) gene, encodes complete protein.
AB045829 - Homo sapiens mRNA for 3alpha-hydroxysteroid dehydrogenase variant, complete cds.
M33375 - Human chlordecone reductase mRNA, complete cds.
D26125 - Homo sapiens mRNA for 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase DD4, partial cds.
JD136992 - Sequence 118016 from Patent EP1572962.
JD496865 - Sequence 477889 from Patent EP1572962.
MB486559 - JP 2019531699-A/6: METHODS FOR DIAGNOSING AND TREATING CANCER.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa00120 - Primary bile acid biosynthesis
hsa00140 - Steroid hormone biosynthesis
hsa00980 - Metabolism of xenobiotics by cytochrome P450
hsa01100 - Metabolic pathways

Reactome (by CSHL, EBI, and GO)

Protein P17516 (Reactome details) participates in the following event(s):

R-HSA-2855252 AKRs reduce RBP2:atRAL to RBP2:atROL
R-HSA-192036 5Beta-cholesten-7alpha, 12alpha-diol-3-one is reduced to 5beta-cholestan-3alpha, 7alpha, 12alpha-triol
R-HSA-192160 5beta-cholestan-7alpha-ol-3-one is reduced to 5beta-cholestan-3alpha, 7alpha-diol
R-HSA-193758 5beta-cholestan-7alpha,24(S)-diol-3-one is reduced to 5beta-cholestan-3alpha,7alpha,24(S)-triol
R-HSA-193781 5Beta-cholestan-7alpha,12alpha,24(S)-triol-3-one is reduced to 5beta-cholestan-3alpha,7alpha,12alpha,24(S)-tetrol
R-HSA-193800 5Beta-cholestan-7alpha,12alpha,27-triol-3-one is reduced to 5beta-cholestan-3alpha,7alpha,12alpha,27-tetrol
R-HSA-193841 5beta-cholestan-7alpha,27-diol-3-one is reduced to 5beta-cholestan-3alpha,7alpha,27-triol
R-HSA-975634 Retinoid metabolism and transport
R-HSA-193368 Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
R-HSA-193775 Synthesis of bile acids and bile salts via 24-hydroxycholesterol
R-HSA-193807 Synthesis of bile acids and bile salts via 27-hydroxycholesterol
R-HSA-2187338 Visual phototransduction
R-HSA-6806667 Metabolism of fat-soluble vitamins
R-HSA-192105 Synthesis of bile acids and bile salts
R-HSA-418594 G alpha (i) signalling events
R-HSA-196854 Metabolism of vitamins and cofactors
R-HSA-194068 Bile acid and bile salt metabolism
R-HSA-388396 GPCR downstream signalling
R-HSA-1430728 Metabolism
R-HSA-8957322 Metabolism of steroids
R-HSA-372790 Signaling by GPCR
R-HSA-556833 Metabolism of lipids
R-HSA-162582 Signal Transduction

-  Other Names for This Gene
  Alternate Gene Symbols: AK1C4_HUMAN, BC020744, CHDR, ENST00000380448.1, ENST00000380448.2, ENST00000380448.3, ENST00000380448.4, P17516, Q5T6A3, Q8WW84, Q9NS54, uc057rjf.1
UCSC ID: ENST00000380448.5
RefSeq Accession: NM_001818.5
Protein: P17516 (aka AK1C4_HUMAN or AKC4_HUMAN)
CCDS: CCDS7064.1

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  Click here for details on how this gene model was made and data restrictions if any.