ACOX2 (acyl-CoA oxidase 2) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: ACOX2 (acyl-CoA oxidase 2) Homo sapiens
Analyze
Symbol: ACOX2
Name: acyl-CoA oxidase 2
RGD ID: 735528
HGNC Page HGNC:120
Description: Enables 3alpha,7alpha,12alpha-trihydroxy-5beta-cholestanoyl-CoA 24-hydroxylase activity. Involved in fatty acid beta-oxidation using acyl-CoA oxidase; positive regulation of cell death; and positive regulation of response to oxidative stress. Located in cytosol and peroxisome. Implicated in congenital bile acid synthesis defect 6.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase; 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA oxidase; acyl-CoA oxidase 2, branched chain; acyl-Coenzyme A oxidase 2, branched chain; BCOX; branched chain acyl-CoA oxidase; BRCACOX; BRCOX; CBAS6; peroxisomal acyl-coenzyme A oxidase 2; peroxisomal branched chain acyl-CoA oxidase; THCA-CoA oxidase; THCCox; trihydroxycoprostanoyl-CoA oxidase
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38358,505,136 - 58,537,190 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl358,505,136 - 58,537,283 (-)EnsemblGRCh38hg38GRCh38
GRCh37358,490,863 - 58,522,917 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36358,465,903 - 58,497,956 (-)NCBINCBI36hg18NCBI36
Build 34358,465,903 - 58,497,956NCBI
Celera358,504,526 - 58,536,479 (-)NCBI
Cytogenetic Map3p14.3NCBI
HuRef358,587,451 - 58,619,350 (-)NCBIHuRef
CHM1_1358,441,069 - 58,473,060 (-)NCBICHM1_1
T2T-CHM13v2.0358,545,514 - 58,577,544 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
1-chloro-2,4-dinitrobenzene  (EXP)
1-naphthyl isothiocyanate  (ISO)
2,3,4,7,8-Pentachlorodibenzofuran  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2-amino-2-deoxy-D-glucopyranose  (ISO)
3-methylcholanthrene  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
5-aza-2'-deoxycytidine  (EXP)
acrylamide  (ISO)
Actein  (ISO)
aflatoxin B1  (EXP)
aldehydo-D-glucosamine  (ISO)
aldehydo-D-glucose  (ISO)
amiodarone  (ISO)
ammonium chloride  (ISO)
antimycin A  (ISO)
antirheumatic drug  (EXP)
benzamides  (EXP)
benzo[a]pyrene  (EXP,ISO)
Benzo[k]fluoranthene  (ISO)
beta-D-glucosamine  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (ISO)
cadmium dichloride  (ISO)
calcitriol  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chloroprene  (ISO)
cisplatin  (EXP,ISO)
clofibric acid  (ISO)
cobalt dichloride  (ISO)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
copper(II) sulfate  (EXP)
cyclosporin A  (EXP,ISO)
D-glucose  (ISO)
dexamethasone  (ISO)
dibenz[a,h]anthracene  (ISO)
dibenzo[a,l]pyrene  (ISO)
difenoconazole  (EXP)
dimethylarsinic acid  (ISO)
doxorubicin  (EXP,ISO)
endosulfan  (ISO)
farnesol  (EXP)
fenofibrate  (ISO)
fludioxonil  (EXP)
fluoranthene  (ISO)
flutamide  (ISO)
genistein  (ISO)
glucose  (ISO)
GW 4064  (EXP)
GW 7647  (EXP)
isotretinoin  (EXP)
methapyrilene  (ISO)
methylarsonic acid  (ISO)
N-methyl-N'-nitro-N-nitrosoguanidine  (ISO)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (ISO)
N-Nitrosopyrrolidine  (EXP)
nickel atom  (EXP)
nickel sulfate  (EXP)
nitrofen  (ISO)
O-methyleugenol  (EXP)
obeticholic acid  (EXP)
okadaic acid  (ISO)
oleic acid  (EXP)
paracetamol  (EXP,ISO)
perfluorohexanesulfonic acid  (ISO)
perfluorononanoic acid  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP,ISO)
phenobarbital  (ISO)
phlorizin  (ISO)
pirinixic acid  (EXP,ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
propiconazole  (EXP,ISO)
quercetin  (EXP,ISO)
rotenone  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP,ISO)
sunitinib  (EXP)
tamoxifen  (ISO)
testosterone  (EXP)
tetrachloromethane  (ISO)
tetracycline  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trichloroethene  (ISO)
Triptolide  (ISO)
valproic acid  (EXP,ISO)
vancomycin  (ISO)
zinc atom  (ISO)
zinc(0)  (ISO)
zoledronic acid  (ISO)

References

References - curated
# Reference Title Reference Citation
1. Polski tygodnik lekarski (Warsaw, Poland : 1960) Dubiel JP and Karczmarz A, Pol Tyg Lek 1978 Aug 7;33(32):1249-51.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
4. SMPDB Annotation Import Pipeline Pipeline to import SMPDB annotations from SMPDB into RGD
5. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
7. [Prevention of sterility in heifers]. Semenchenko NA, Veterinariia. 1978 Dec;(12):83-4.
Additional References at PubMed
PMID:2079609   PMID:8387517   PMID:8943006   PMID:8993592   PMID:9070889   PMID:12477932   PMID:15489334   PMID:16756494   PMID:20178365   PMID:20379614   PMID:21343950   PMID:21873635  
PMID:26167880   PMID:26183823   PMID:27884763   PMID:28514442   PMID:29971632   PMID:32296183   PMID:33414412   PMID:33961781  


Genomics

Comparative Map Data
ACOX2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38358,505,136 - 58,537,190 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl358,505,136 - 58,537,283 (-)EnsemblGRCh38hg38GRCh38
GRCh37358,490,863 - 58,522,917 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36358,465,903 - 58,497,956 (-)NCBINCBI36hg18NCBI36
Build 34358,465,903 - 58,497,956NCBI
Celera358,504,526 - 58,536,479 (-)NCBI
Cytogenetic Map3p14.3NCBI
HuRef358,587,451 - 58,619,350 (-)NCBIHuRef
CHM1_1358,441,069 - 58,473,060 (-)NCBICHM1_1
T2T-CHM13v2.0358,545,514 - 58,577,544 (-)NCBI
Acox2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391414,210,406 - 14,244,262 (+)NCBIGRCm39mm39
GRCm39 Ensembl1414,210,420 - 14,244,262 (+)Ensembl
GRCm38148,225,511 - 8,259,019 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl148,225,511 - 8,259,353 (-)EnsemblGRCm38mm10GRCm38
MGSCv37149,058,025 - 9,091,533 (-)NCBIGRCm37mm9NCBIm37
MGSCv36147,019,267 - 7,052,692 (-)NCBImm8
Celera143,848,464 - 3,882,056 (-)NCBICelera
Cytogenetic Map14A1NCBI
Acox2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21516,660,584 - 16,692,160 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl1516,660,272 - 16,692,160 (+)Ensembl
Rnor_6.01518,449,304 - 18,481,472 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1518,451,144 - 18,481,470 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01522,418,099 - 22,449,500 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41518,645,349 - 18,677,855 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11518,645,348 - 18,677,855 (+)NCBI
Celera1516,620,632 - 16,652,578 (+)NCBICelera
Cytogenetic Map15p14NCBI
Acox2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554301,638,431 - 1,665,141 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554301,638,931 - 1,665,308 (+)NCBIChiLan1.0ChiLan1.0
ACOX2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1359,852,771 - 59,884,548 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl359,852,771 - 59,884,548 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0358,442,532 - 58,474,601 (-)NCBIMhudiblu_PPA_v0panPan3
ACOX2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12032,110,788 - 32,141,751 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2032,113,217 - 32,141,734 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2032,035,767 - 32,068,722 (+)NCBI
ROS_Cfam_1.02032,378,012 - 32,411,337 (+)NCBI
ROS_Cfam_1.0 Ensembl2032,378,302 - 32,410,072 (+)Ensembl
UMICH_Zoey_3.12031,836,223 - 31,868,139 (+)NCBI
UNSW_CanFamBas_1.02032,191,158 - 32,224,121 (+)NCBI
UU_Cfam_GSD_1.02032,363,394 - 32,396,348 (+)NCBI
Acox2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118169,355,964 - 169,386,915 (+)NCBI
SpeTri2.0NW_0049364732,494,568 - 2,525,956 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ACOX2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1340,223,010 - 40,255,967 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11340,220,952 - 40,255,967 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21344,232,258 - 44,264,976 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ACOX2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12219,805,736 - 19,838,399 (-)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl2219,804,440 - 19,838,374 (-)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666041146,983,928 - 147,016,629 (+)NCBIVero_WHO_p1.0
Acox2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248225,536,421 - 5,561,781 (-)EnsemblHetGla_female_1.0hetGla2
HetGla 1.0NW_0046248225,535,086 - 5,561,867 (-)NCBIHetGla_female_1.0hetGla2

Position Markers
SHGC-33100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37358,490,881 - 58,491,005UniSTSGRCh37
Build 36358,465,921 - 58,466,045RGDNCBI36
Celera358,504,544 - 58,504,668RGD
Cytogenetic Map3p14.3UniSTS
HuRef358,587,469 - 58,587,593UniSTS
TNG Radiation Hybrid Map335966.0UniSTS
GeneMap99-G3 RH Map32627.0UniSTS
RH71302  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p14.3UniSTS
GeneMap99-GB4 RH Map3198.02UniSTS
NCBI RH Map3594.2UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2354
Count of miRNA genes:944
Interacting mature miRNAs:1155
Transcripts:ENST00000302819, ENST00000459701, ENST00000459888, ENST00000460921, ENST00000466689, ENST00000466810, ENST00000467738, ENST00000474098, ENST00000475143, ENST00000480791, ENST00000481527, ENST00000489472, ENST00000492530
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 1865 1763 1468 462 172 405 2089 1120 804 210 1100 976 58 961 1350
Low 527 835 243 154 751 49 2216 1042 2851 157 274 505 105 243 1437 2
Below cutoff 28 377 7 6 507 9 42 17 42 37 55 83 6 1 1 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_052668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005265505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006713340 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024453786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449042 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC116036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ001541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC033517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG698950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI490007 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HB873093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HB882955 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HB894284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HC930502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HC940364 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HC951693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X95190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000302819   ⟹   ENSP00000307697
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,505,136 - 58,537,190 (-)Ensembl
RefSeq Acc Id: ENST00000459701   ⟹   ENSP00000418562
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,505,136 - 58,537,283 (-)Ensembl
RefSeq Acc Id: ENST00000459888
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,526,505 - 58,529,206 (-)Ensembl
RefSeq Acc Id: ENST00000460921   ⟹   ENSP00000417877
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,505,138 - 58,517,387 (-)Ensembl
RefSeq Acc Id: ENST00000466689
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,534,118 - 58,537,175 (-)Ensembl
RefSeq Acc Id: ENST00000466810
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,531,310 - 58,533,825 (-)Ensembl
RefSeq Acc Id: ENST00000467738
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,505,136 - 58,526,749 (-)Ensembl
RefSeq Acc Id: ENST00000474098   ⟹   ENSP00000419927
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,533,514 - 58,537,178 (-)Ensembl
RefSeq Acc Id: ENST00000475143
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,534,058 - 58,537,172 (-)Ensembl
RefSeq Acc Id: ENST00000480791
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,534,577 - 58,537,147 (-)Ensembl
RefSeq Acc Id: ENST00000481527
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,505,136 - 58,522,987 (-)Ensembl
RefSeq Acc Id: ENST00000489472   ⟹   ENSP00000418515
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,524,462 - 58,533,553 (-)Ensembl
RefSeq Acc Id: ENST00000492530   ⟹   ENSP00000419133
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl358,531,321 - 58,534,979 (-)Ensembl
RefSeq Acc Id: NM_003500   ⟹   NP_003491
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38358,505,136 - 58,537,190 (-)NCBI
GRCh37358,490,863 - 58,522,929 (-)RGD
Build 36358,465,903 - 58,497,956 (-)NCBI Archive
Celera358,504,526 - 58,536,479 (-)RGD
HuRef358,587,451 - 58,619,350 (-)ENTREZGENE
CHM1_1358,441,069 - 58,473,060 (-)NCBI
T2T-CHM13v2.0358,545,514 - 58,577,544 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005265505   ⟹   XP_005265562
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38358,505,136 - 58,537,190 (-)NCBI
GRCh37358,490,863 - 58,522,929 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006713340   ⟹   XP_006713403
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38358,505,136 - 58,535,029 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047449042   ⟹   XP_047304998
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38358,505,136 - 58,537,190 (-)NCBI
Reference Sequences
RefSeq Acc Id: NP_003491   ⟸   NM_003500
- UniProtKB: Q99424 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005265562   ⟸   XM_005265505
- Peptide Label: isoform X2
- UniProtKB: Q99424 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006713403   ⟸   XM_006713340
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000419133   ⟸   ENST00000492530
RefSeq Acc Id: ENSP00000418562   ⟸   ENST00000459701
RefSeq Acc Id: ENSP00000307697   ⟸   ENST00000302819
RefSeq Acc Id: ENSP00000419927   ⟸   ENST00000474098
RefSeq Acc Id: ENSP00000417877   ⟸   ENST00000460921
RefSeq Acc Id: ENSP00000418515   ⟸   ENST00000489472
RefSeq Acc Id: XP_047304998   ⟸   XM_047449042
- Peptide Label: isoform X1
Protein Domains
ACOX   Acyl-CoA_dh_M   Acyl-CoA_ox_N

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q99424-F1-model_v2 AlphaFold Q99424 1-681 view protein structure

Promoters
RGD ID:6864880
Promoter ID:EPDNEW_H5583
Type:initiation region
Name:ACOX2_1
Description:acyl-CoA oxidase 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H5584  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38358,537,190 - 58,537,250EPDNEW
RGD ID:6864838
Promoter ID:EPDNEW_H5584
Type:initiation region
Name:ACOX2_2
Description:acyl-CoA oxidase 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H5583  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38358,537,366 - 58,537,426EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3p14.3-14.2(chr3:58532827-60193441)x3 copy number gain See cases [RCV000051469] Chr3:58532827..60193441 [GRCh38]
Chr3:58518554..60179169 [GRCh37]
Chr3:58493594..60154209 [NCBI36]
Chr3:3p14.3-14.2
uncertain significance
GRCh38/hg38 3p21.1-14.1(chr3:54045018-66060461)x1 copy number loss See cases [RCV000051081] Chr3:54045018..66060461 [GRCh38]
Chr3:54079045..66046136 [GRCh37]
Chr3:54054085..66021176 [NCBI36]
Chr3:3p21.1-14.1
pathogenic
NM_001128214.1(KCTD6):c.611C>T (p.Thr204Met) single nucleotide variant Malignant melanoma [RCV000060853] Chr3:58501529 [GRCh38]
Chr3:58487256 [GRCh37]
Chr3:58462296 [NCBI36]
Chr3:3p14.3
not provided
GRCh38/hg38 3p14.3-14.1(chr3:57430538-64884522)x1 copy number loss See cases [RCV000139570] Chr3:57430538..64884522 [GRCh38]
Chr3:57416265..64870197 [GRCh37]
Chr3:57391305..64845237 [NCBI36]
Chr3:3p14.3-14.1
pathogenic
GRCh38/hg38 3p14.3-11.1(chr3:57140424-90259960)x1 copy number loss See cases [RCV000139626] Chr3:57140424..90259960 [GRCh38]
Chr3:57174452..90309110 [GRCh37]
Chr3:57149492..90391800 [NCBI36]
Chr3:3p14.3-11.1
pathogenic
GRCh38/hg38 3p14.3-14.2(chr3:58498793-60217173)x3 copy number gain See cases [RCV000142126] Chr3:58498793..60217173 [GRCh38]
Chr3:58484520..60202901 [GRCh37]
Chr3:58459560..60177941 [NCBI36]
Chr3:3p14.3-14.2
uncertain significance
GRCh38/hg38 3p14.3-14.2(chr3:58534847-60199939)x3 copy number gain See cases [RCV000142665] Chr3:58534847..60199939 [GRCh38]
Chr3:58520574..60185667 [GRCh37]
Chr3:58495614..60160707 [NCBI36]
Chr3:3p14.3-14.2
uncertain significance
GRCh37/hg19 3p14.3-14.2(chr3:58494677-60076736)x3 copy number gain See cases [RCV000240101] Chr3:58494677..60076736 [GRCh37]
Chr3:3p14.3-14.2
uncertain significance
GRCh37/hg19 3p21.2-14.2(chr3:52086599-59689209)x1 copy number loss See cases [RCV000239886] Chr3:52086599..59689209 [GRCh37]
Chr3:3p21.2-14.2
pathogenic
NM_003500.4(ACOX2):c.207T>A (p.Tyr69Ter) single nucleotide variant Congenital bile acid synthesis defect 6 [RCV000416307] Chr3:58534476 [GRCh38]
Chr3:58520203 [GRCh37]
Chr3:3p14.3
pathogenic
NM_003500.4(ACOX2):c.149G>A (p.Arg50His) single nucleotide variant Congenital bile acid synthesis defect 6 [RCV000681659] Chr3:58534958 [GRCh38]
Chr3:58520685 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.673C>T (p.Arg225Trp) single nucleotide variant Congenital bile acid synthesis defect 6 [RCV000417194]|not provided [RCV001865316] Chr3:58531723 [GRCh38]
Chr3:58517450 [GRCh37]
Chr3:3p14.3
pathogenic|likely pathogenic|uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3 copy number gain See cases [RCV000511055] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p14.3-14.2(chr3:58498676-60210851)x3 copy number gain not provided [RCV000682261] Chr3:58498676..60210851 [GRCh37]
Chr3:3p14.3-14.2
uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3 copy number gain not provided [RCV000742138] Chr3:61495..197838262 [GRCh37]
Chr3:3p26.3-q29
pathogenic
NM_003500.4(ACOX2):c.-26T>C single nucleotide variant Congenital bile acid synthesis defect 6 [RCV001548953] Chr3:58535132 [GRCh38]
Chr3:58520859 [GRCh37]
Chr3:3p14.3
benign
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3 copy number gain not provided [RCV000742133] Chr3:60174..197948027 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p14.3-14.2(chr3:58089516-58799748)x3 copy number gain not provided [RCV000742425] Chr3:58089516..58799748 [GRCh37]
Chr3:3p14.3-14.2
benign
NM_003500.4(ACOX2):c.339C>T (p.Asp113=) single nucleotide variant not provided [RCV000926612] Chr3:58534130 [GRCh38]
Chr3:58519857 [GRCh37]
Chr3:3p14.3
likely benign
GRCh37/hg19 3p14.3-14.2(chr3:58490107-60210773)x3 copy number gain not provided [RCV000848569] Chr3:58490107..60210773 [GRCh37]
Chr3:3p14.3-14.2
uncertain significance
GRCh37/hg19 3p14.3-14.2(chr3:58490107-60210773)x3 copy number gain not provided [RCV000848572] Chr3:58490107..60210773 [GRCh37]
Chr3:3p14.3-14.2
uncertain significance
NM_003500.4(ACOX2):c.867C>T (p.Asn289=) single nucleotide variant not provided [RCV000895937] Chr3:58530591 [GRCh38]
Chr3:58516318 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.103C>T (p.Arg35Trp) single nucleotide variant not provided [RCV000960838] Chr3:58535004 [GRCh38]
Chr3:58520731 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.28T>C (p.Leu10=) single nucleotide variant not provided [RCV000891969] Chr3:58535079 [GRCh38]
Chr3:58520806 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.161-57C>G single nucleotide variant Congenital bile acid synthesis defect 6 [RCV001548952] Chr3:58534579 [GRCh38]
Chr3:58520306 [GRCh37]
Chr3:3p14.3
benign
GRCh37/hg19 3p14.3-14.2(chr3:58490107-60210773)x3 copy number gain not provided [RCV000846903] Chr3:58490107..60210773 [GRCh37]
Chr3:3p14.3-14.2
uncertain significance
GRCh37/hg19 3p14.3-14.1(chr3:57076136-65716956)x1 copy number loss not provided [RCV000846379] Chr3:57076136..65716956 [GRCh37]
Chr3:3p14.3-14.1
pathogenic
NM_003500.4(ACOX2):c.450G>A (p.Thr150=) single nucleotide variant not provided [RCV000907101] Chr3:58534019 [GRCh38]
Chr3:58519746 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.12A>C (p.Pro4=) single nucleotide variant not provided [RCV000909711] Chr3:58535095 [GRCh38]
Chr3:58520822 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.324-4A>G single nucleotide variant not provided [RCV000979304] Chr3:58534149 [GRCh38]
Chr3:58519876 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.850G>A (p.Gly284Ser) single nucleotide variant not provided [RCV000903730] Chr3:58530608 [GRCh38]
Chr3:58516335 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.461_464del (p.Thr154fs) microsatellite Congenital bile acid synthesis defect 6 [RCV001784474]|not provided [RCV000882237] Chr3:58534005..58534008 [GRCh38]
Chr3:58519732..58519735 [GRCh37]
Chr3:3p14.3
likely pathogenic|benign
NM_003500.4(ACOX2):c.1983+7G>C single nucleotide variant not provided [RCV000895110] Chr3:58508886 [GRCh38]
Chr3:58494613 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.1485C>T (p.Cys495=) single nucleotide variant not provided [RCV000948651] Chr3:58524467 [GRCh38]
Chr3:58510194 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.713T>C (p.Ile238Thr) single nucleotide variant not provided [RCV000973341] Chr3:58531357 [GRCh38]
Chr3:58517084 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.1186A>G (p.Met396Val) single nucleotide variant not provided [RCV000912432] Chr3:58526626 [GRCh38]
Chr3:58512353 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.1992T>G (p.Pro664=) single nucleotide variant not provided [RCV000913910] Chr3:58505278 [GRCh38]
Chr3:58491005 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.1346+8C>G single nucleotide variant not provided [RCV000934276] Chr3:58526458 [GRCh38]
Chr3:58512185 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.97G>A (p.Val33Met) single nucleotide variant not provided [RCV000911827] Chr3:58535010 [GRCh38]
Chr3:58520737 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.380G>A (p.Arg127Lys) single nucleotide variant Congenital bile acid synthesis defect 6 [RCV001336582] Chr3:58534089 [GRCh38]
Chr3:58519816 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.182C>T (p.Pro61Leu) single nucleotide variant Congenital bile acid synthesis defect 6 [RCV001733601] Chr3:58534501 [GRCh38]
Chr3:58520228 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.1693G>C (p.Glu565Gln) single nucleotide variant not provided [RCV001815924] Chr3:58517363 [GRCh38]
Chr3:58503090 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1327C>T (p.Leu443Phe) single nucleotide variant not provided [RCV001949842] Chr3:58526485 [GRCh38]
Chr3:58512212 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.589C>T (p.Arg197Trp) single nucleotide variant not provided [RCV001947680] Chr3:58531807 [GRCh38]
Chr3:58517534 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.952C>T (p.Arg318Cys) single nucleotide variant not provided [RCV001892579] Chr3:58530506 [GRCh38]
Chr3:58516233 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1156-3C>G single nucleotide variant not provided [RCV001947923] Chr3:58526659 [GRCh38]
Chr3:58512386 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1087A>T (p.Ser363Cys) single nucleotide variant not provided [RCV001912285] Chr3:58528862 [GRCh38]
Chr3:58514589 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1474G>A (p.Asp492Asn) single nucleotide variant not provided [RCV002003650] Chr3:58524478 [GRCh38]
Chr3:58510205 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1633-2A>G single nucleotide variant not provided [RCV002001216] Chr3:58517425 [GRCh38]
Chr3:58503152 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1528C>T (p.Leu510Phe) single nucleotide variant not provided [RCV001943287] Chr3:58522600 [GRCh38]
Chr3:58508327 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1226G>A (p.Arg409His) single nucleotide variant not provided [RCV001940828] Chr3:58526586 [GRCh38]
Chr3:58512313 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.967C>T (p.Arg323Cys) single nucleotide variant not provided [RCV001971866] Chr3:58530491 [GRCh38]
Chr3:58516218 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.964A>G (p.Ile322Val) single nucleotide variant not provided [RCV002010129] Chr3:58530494 [GRCh38]
Chr3:58516221 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.704-3A>C single nucleotide variant not provided [RCV001904583] Chr3:58531369 [GRCh38]
Chr3:58517096 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.953G>A (p.Arg318His) single nucleotide variant not provided [RCV002027046] Chr3:58530505 [GRCh38]
Chr3:58516232 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.781C>T (p.Arg261Trp) single nucleotide variant not provided [RCV001907346] Chr3:58531289 [GRCh38]
Chr3:58517016 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.160+5G>A single nucleotide variant not provided [RCV001924840] Chr3:58534942 [GRCh38]
Chr3:58520669 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1582C>G (p.Gln528Glu) single nucleotide variant not provided [RCV001921445] Chr3:58522546 [GRCh38]
Chr3:58508273 [GRCh37]
Chr3:3p14.3
uncertain significance
NM_003500.4(ACOX2):c.1851-4C>T single nucleotide variant not provided [RCV002106084] Chr3:58509029 [GRCh38]
Chr3:58494756 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.820-18C>T single nucleotide variant not provided [RCV002189264] Chr3:58530656 [GRCh38]
Chr3:58516383 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.583+19C>G single nucleotide variant not provided [RCV002127273] Chr3:58533426 [GRCh38]
Chr3:58519153 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.1984-9T>C single nucleotide variant not provided [RCV002089662] Chr3:58505295 [GRCh38]
Chr3:58491022 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.1164A>G (p.Ala388=) single nucleotide variant not provided [RCV002205839] Chr3:58526648 [GRCh38]
Chr3:58512375 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.992+13C>T single nucleotide variant not provided [RCV002196057] Chr3:58530453 [GRCh38]
Chr3:58516180 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.946G>A (p.Ala316Thr) single nucleotide variant not provided [RCV002125919] Chr3:58530512 [GRCh38]
Chr3:58516239 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.1293G>A (p.Ser431=) single nucleotide variant not provided [RCV002109110] Chr3:58526519 [GRCh38]
Chr3:58512246 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.180C>T (p.Tyr60=) single nucleotide variant not provided [RCV002188327] Chr3:58534503 [GRCh38]
Chr3:58520230 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.324-15A>C single nucleotide variant not provided [RCV002148514] Chr3:58534160 [GRCh38]
Chr3:58519887 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.1156-14C>T single nucleotide variant not provided [RCV002152793] Chr3:58526670 [GRCh38]
Chr3:58512397 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.603T>C (p.His201=) single nucleotide variant not provided [RCV002174223] Chr3:58531793 [GRCh38]
Chr3:58517520 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.475+18C>T single nucleotide variant not provided [RCV002079703] Chr3:58533976 [GRCh38]
Chr3:58519703 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.1302T>C (p.Cys434=) single nucleotide variant not provided [RCV002117953] Chr3:58526510 [GRCh38]
Chr3:58512237 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.1156-16del deletion not provided [RCV002122653] Chr3:58526672 [GRCh38]
Chr3:58512399 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.1764G>A (p.Ser588=) single nucleotide variant not provided [RCV002217446] Chr3:58517292 [GRCh38]
Chr3:58503019 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.108C>T (p.Leu36=) single nucleotide variant not provided [RCV002081584] Chr3:58534999 [GRCh38]
Chr3:58520726 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.475+19G>A single nucleotide variant not provided [RCV002102255] Chr3:58533975 [GRCh38]
Chr3:58519702 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.1254A>G (p.Ser418=) single nucleotide variant not provided [RCV002117949] Chr3:58526558 [GRCh38]
Chr3:58512285 [GRCh37]
Chr3:3p14.3
benign
NM_003500.4(ACOX2):c.1346+7T>C single nucleotide variant not provided [RCV002141012] Chr3:58526459 [GRCh38]
Chr3:58512186 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.1341G>A (p.Val447=) single nucleotide variant not provided [RCV002160021] Chr3:58526471 [GRCh38]
Chr3:58512198 [GRCh37]
Chr3:3p14.3
likely benign
NM_003500.4(ACOX2):c.323+2T>C single nucleotide variant Congenital bile acid synthesis defect 6 [RCV002250944] Chr3:58534358 [GRCh38]
Chr3:58520085 [GRCh37]
Chr3:3p14.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:120 AgrOrtholog
COSMIC ACOX2 COSMIC
Ensembl Genes ENSG00000168306 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000307697 ENTREZGENE
  ENSP00000307697.5 UniProtKB/Swiss-Prot
  ENSP00000417877.1 UniProtKB/TrEMBL
  ENSP00000418515.1 UniProtKB/TrEMBL
  ENSP00000418562.2 UniProtKB/TrEMBL
  ENSP00000419133.1 UniProtKB/TrEMBL
  ENSP00000419927.1 UniProtKB/TrEMBL
Ensembl Transcript ENST00000302819 ENTREZGENE
  ENST00000302819.10 UniProtKB/Swiss-Prot
  ENST00000459701.6 UniProtKB/TrEMBL
  ENST00000460921.1 UniProtKB/TrEMBL
  ENST00000474098.1 UniProtKB/TrEMBL
  ENST00000489472.1 UniProtKB/TrEMBL
  ENST00000492530.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.540.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.40.110.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000168306 GTEx
HGNC ID HGNC:120 ENTREZGENE
Human Proteome Map ACOX2 Human Proteome Map
InterPro Acyl-CoA_ox_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Acyl-CoA_Oxase/DH_cen-dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Acyl-CoA_Oxase/DH_mid-dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Acyl-CoA_oxidase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Acyl-CoA_oxidase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AcylCo_DH-like_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AcylCoA_DH/ox_N_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AcylCoA_DH/oxidase_NM_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8309 UniProtKB/Swiss-Prot
NCBI Gene 8309 ENTREZGENE
OMIM 601641 OMIM
  617308 OMIM
PANTHER PTHR10909 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam ACOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Acyl-CoA_dh_M UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Acyl-CoA_ox_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA24444 PharmGKB
PIRSF Acyl-CoA_oxidase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47203 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF56645 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt ACOX2_HUMAN UniProtKB/Swiss-Prot
  C9J0G0_HUMAN UniProtKB/TrEMBL
  C9JY29_HUMAN UniProtKB/TrEMBL
  H7C4Q2_HUMAN UniProtKB/TrEMBL
  H7C4Y2_HUMAN UniProtKB/TrEMBL
  H7C573_HUMAN UniProtKB/TrEMBL
  Q99424 ENTREZGENE
UniProt Secondary A6NF16 UniProtKB/Swiss-Prot
  B2R8U5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-07 ACOX2  acyl-CoA oxidase 2    acyl-CoA oxidase 2, branched chain  Symbol and/or name change 5135510 APPROVED
2011-09-01 ACOX2  acyl-CoA oxidase 2, branched chain  ACOX2  acyl-CoA oxidase 2, branched chain  Symbol and/or name change 5135510 APPROVED
2011-07-27 ACOX2  acyl-CoA oxidase 2, branched chain  ACOX2  acyl-Coenzyme A oxidase 2, branched chain  Symbol and/or name change 5135510 APPROVED