SUOX (sulfite oxidase) - Rat Genome Database

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Gene: SUOX (sulfite oxidase) Homo sapiens
Analyze
Symbol: SUOX
Name: sulfite oxidase
RGD ID: 733312
HGNC Page HGNC
Description: Predicted to enable heme binding activity; molybdopterin cofactor binding activity; and sulfite oxidase activity. Predicted to be involved in sulfur compound metabolic process. Predicted to be located in mitochondrial matrix. Predicted to be active in mitochondrion. Implicated in inherited metabolic disorder and isolated sulfite oxidase deficiency.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: sulfite oxidase, mitochondrial
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: AC090132.1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1255,997,180 - 56,006,641 (+)EnsemblGRCh38hg38GRCh38
GRCh381255,992,547 - 56,005,525 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371256,391,060 - 56,399,309 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361254,677,310 - 54,685,576 (+)NCBINCBI36hg18NCBI36
Build 341254,681,548 - 54,685,109NCBI
Celera1256,043,727 - 56,051,993 (+)NCBI
Cytogenetic Map12q13.2NCBI
HuRef1253,429,929 - 53,438,195 (+)NCBIHuRef
CHM1_11256,358,154 - 56,366,418 (+)NCBICHM1_1
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)
(-)-epigallocatechin 3-gallate  (EXP)
1,1-dichloroethene  (ISO)
1,2-dimethylhydrazine  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-methylcholine  (EXP)
3-chloropropane-1,2-diol  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4-hydroxyphenyl retinamide  (ISO)
4-octylphenol  (EXP)
acetamide  (ISO)
aflatoxin B1  (ISO)
all-trans-retinoic acid  (EXP)
ammonium chloride  (ISO)
avobenzone  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (EXP,ISO)
cadmium dichloride  (ISO)
carbon nanotube  (ISO)
chromium(6+)  (ISO)
cisplatin  (ISO)
cobalt dichloride  (ISO)
copper(II) sulfate  (EXP)
cyclosporin A  (EXP)
dextran sulfate  (ISO)
diazinon  (EXP)
Diisodecyl phthalate  (EXP)
dioscin  (ISO)
fipronil  (ISO)
fluoranthene  (ISO)
flutamide  (ISO)
folic acid  (ISO)
furan  (ISO)
glafenine  (ISO)
hydrogen peroxide  (EXP)
ivermectin  (EXP)
ketamine  (ISO)
menadione  (EXP)
mercury dichloride  (ISO)
methapyrilene  (ISO)
N-nitrosodiethylamine  (ISO)
N-nitrosomorpholine  (ISO)
nefazodone  (ISO)
nimesulide  (ISO)
nitrofen  (ISO)
paracetamol  (EXP,ISO)
paraquat  (ISO)
perfluorododecanoic acid  (ISO)
perfluorononanoic acid  (EXP)
pirinixic acid  (ISO)
potassium chromate  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
propiconazole  (ISO)
quercetin  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (ISO)
sunitinib  (EXP)
T-2 toxin  (ISO)
tert-butyl hydroperoxide  (EXP)
tetrachloromethane  (ISO)
titanium dioxide  (ISO)
tunicamycin  (EXP)
valdecoxib  (ISO)
valproic acid  (EXP,ISO)
vancomycin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:7599189   PMID:9428520   PMID:9600976   PMID:10519592   PMID:12368985   PMID:12424234   PMID:12477932   PMID:12763039   PMID:12832761   PMID:14567685   PMID:14729666   PMID:15489334  
PMID:16140720   PMID:16229463   PMID:16344560   PMID:16475804   PMID:17366837   PMID:17940249   PMID:18177044   PMID:18198356   PMID:18529001   PMID:18959753   PMID:20063894   PMID:20491442  
PMID:20877624   PMID:21873635   PMID:21988832   PMID:22263579   PMID:22885925   PMID:22951725   PMID:22975842   PMID:23665285   PMID:24106282   PMID:24390342   PMID:24968320   PMID:25314640  
PMID:25910212   PMID:26171830   PMID:26186194   PMID:27289259   PMID:28514442   PMID:28629418   PMID:28933809   PMID:29280012   PMID:29791485   PMID:30631948   PMID:31127934   PMID:32235678  
PMID:32296183   PMID:34079125  


Genomics

Comparative Map Data
SUOX
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1255,997,180 - 56,006,641 (+)EnsemblGRCh38hg38GRCh38
GRCh381255,992,547 - 56,005,525 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371256,391,060 - 56,399,309 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361254,677,310 - 54,685,576 (+)NCBINCBI36hg18NCBI36
Build 341254,681,548 - 54,685,109NCBI
Celera1256,043,727 - 56,051,993 (+)NCBI
Cytogenetic Map12q13.2NCBI
HuRef1253,429,929 - 53,438,195 (+)NCBIHuRef
CHM1_11256,358,154 - 56,366,418 (+)NCBICHM1_1
Suox
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3910128,505,756 - 128,509,787 (-)NCBIGRCm39mm39
GRCm39 Ensembl10128,505,763 - 128,509,942 (-)Ensembl
GRCm3810128,669,887 - 128,673,918 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl10128,669,894 - 128,674,073 (-)EnsemblGRCm38mm10GRCm38
MGSCv3710128,106,943 - 128,110,974 (-)NCBIGRCm37mm9NCBIm37
MGSCv3610128,072,843 - 128,076,810 (-)NCBImm8
Celera10131,061,992 - 131,066,023 (-)NCBICelera
Cytogenetic Map10D3NCBI
Suox
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.271,103,149 - 1,107,156 (-)NCBImRatBN7.2
mRatBN7.2 Ensembl71,103,151 - 1,107,038 (-)Ensembl
Rnor_6.073,098,228 - 3,102,179 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl73,098,245 - 3,102,142 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.073,070,928 - 3,074,829 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.471,973,471 - 1,976,040 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.171,973,472 - 1,976,040 (-)NCBI
Celera7973,358 - 975,927 (-)NCBICelera
Cytogenetic Map7q11NCBI
Suox
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554583,585,482 - 3,590,559 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554583,584,390 - 3,589,764 (+)NCBIChiLan1.0ChiLan1.0
SUOX
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11233,157,277 - 33,165,712 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1233,157,277 - 33,165,661 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01232,907,456 - 32,915,788 (-)NCBIMhudiblu_PPA_v0panPan3
SUOX
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.110327,656 - 331,826 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl10327,671 - 331,825 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha10389,623 - 393,749 (+)NCBI
ROS_Cfam_1.010334,299 - 338,424 (+)NCBI
UMICH_Zoey_3.110312,312 - 316,438 (+)NCBI
UNSW_CanFamBas_1.010554,865 - 558,990 (+)NCBI
UU_Cfam_GSD_1.010679,365 - 683,493 (+)NCBI
Suox
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494558,454,620 - 58,458,747 (-)NCBI
SpeTri2.0NW_004936646411,543 - 415,709 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SUOX
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl521,395,282 - 21,399,715 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1521,395,246 - 21,399,715 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
SUOX
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11151,935,809 - 51,943,090 (+)NCBI
ChlSab1.1 Ensembl1151,939,809 - 51,942,603 (+)Ensembl
Vero_WHO_p1.0NW_023666037194,044,119 - 194,051,273 (-)NCBI
Suox
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462480212,049,787 - 12,054,810 (-)NCBI

Position Markers
RH44785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,399,020 - 56,399,282UniSTSGRCh37
Build 361254,685,287 - 54,685,549RGDNCBI36
Celera1256,051,704 - 56,051,966RGD
Cytogenetic Map12q13.2UniSTS
HuRef1253,437,906 - 53,438,168UniSTS
GeneMap99-GB4 RH Map12245.84UniSTS
SHGC-76317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,398,639 - 56,398,778UniSTSGRCh37
Build 361254,684,906 - 54,685,045RGDNCBI36
Celera1256,051,323 - 56,051,462RGD
Cytogenetic Map12q13.2UniSTS
HuRef1253,437,525 - 53,437,664UniSTS
TNG Radiation Hybrid Map1226258.0UniSTS
GeneMap99-GB4 RH Map1696.63UniSTS
NCBI RH Map11880.4UniSTS
STS-AA026389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,399,083 - 56,399,268UniSTSGRCh37
Build 361254,685,350 - 54,685,535RGDNCBI36
Celera1256,051,767 - 56,051,952RGD
Cytogenetic Map12q13.2UniSTS
HuRef1253,437,969 - 53,438,154UniSTS
GeneMap99-GB4 RH Map12250.04UniSTS
RH71366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,398,640 - 56,398,817UniSTSGRCh37
Build 361254,684,907 - 54,685,084RGDNCBI36
Celera1256,051,324 - 56,051,501RGD
Cytogenetic Map12q13.2UniSTS
HuRef1253,437,526 - 53,437,703UniSTS
GeneMap99-GB4 RH Map12247.74UniSTS
Suox  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371256,397,571 - 56,398,521UniSTSGRCh37
Celera1256,050,255 - 56,051,205UniSTS
HuRef1253,436,457 - 53,437,407UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3924
Count of miRNA genes:976
Interacting mature miRNAs:1188
Transcripts:ENST00000266971, ENST00000356124, ENST00000394109, ENST00000394115, ENST00000546712, ENST00000546833, ENST00000547586, ENST00000548274, ENST00000550065, ENST00000550121, ENST00000550340, ENST00000550478, ENST00000551698, ENST00000551841, ENST00000552258, ENST00000552363, ENST00000552813
Prediction methods:Microtar, Miranda, Rnahybrid
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 pharyngeal arch
High
Medium 2218 1688 1648 578 749 427 2766 1449 2145 367 1119 1363 159 1 1032 1736 4 2
Low 221 1292 78 46 1188 38 1591 748 1589 52 341 250 15 172 1052 2
Below cutoff 11 14

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_008136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_000456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001032386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001032387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC034102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AU121557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AU126450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY056018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC065193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF583487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM013717 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L31573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000266971   ⟹   ENSP00000266971
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,276 - 56,005,525 (+)Ensembl
RefSeq Acc Id: ENST00000356124   ⟹   ENSP00000348440
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,180 - 56,005,525 (+)Ensembl
RefSeq Acc Id: ENST00000394109   ⟹   ENSP00000377668
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,001,498 - 56,005,525 (+)Ensembl
RefSeq Acc Id: ENST00000394115   ⟹   ENSP00000377674
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,288 - 56,005,486 (+)Ensembl
RefSeq Acc Id: ENST00000546712
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,001,739 - 56,003,734 (+)Ensembl
RefSeq Acc Id: ENST00000546833   ⟹   ENSP00000449872
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,330 - 56,003,874 (+)Ensembl
RefSeq Acc Id: ENST00000547586   ⟹   ENSP00000448637
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,289 - 56,002,620 (+)Ensembl
RefSeq Acc Id: ENST00000548274   ⟹   ENSP00000450245
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,298 - 56,005,525 (+)Ensembl
RefSeq Acc Id: ENST00000550065   ⟹   ENSP00000450264
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1256,002,214 - 56,006,641 (+)Ensembl
RefSeq Acc Id: ENST00000550121
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,259 - 56,001,905 (+)Ensembl
RefSeq Acc Id: ENST00000550340
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,287 - 56,004,067 (+)Ensembl
RefSeq Acc Id: ENST00000550478
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,319 - 56,003,923 (+)Ensembl
RefSeq Acc Id: ENST00000551698
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,259 - 56,003,965 (+)Ensembl
RefSeq Acc Id: ENST00000551841   ⟹   ENSP00000449443
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,615 - 56,004,673 (+)Ensembl
RefSeq Acc Id: ENST00000552258   ⟹   ENSP00000450049
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,296 - 56,003,752 (+)Ensembl
RefSeq Acc Id: ENST00000552363
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,259 - 56,003,813 (+)Ensembl
RefSeq Acc Id: ENST00000552813
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1255,997,318 - 56,003,054 (+)Ensembl
RefSeq Acc Id: NM_000456   ⟹   NP_000447
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381255,997,276 - 56,005,525 (+)NCBI
GRCh371256,391,043 - 56,399,309 (+)ENTREZGENE
Build 361254,677,310 - 54,685,576 (+)NCBI Archive
HuRef1253,429,929 - 53,438,195 (+)ENTREZGENE
CHM1_11256,358,154 - 56,366,418 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001032386   ⟹   NP_001027558
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381255,997,276 - 56,005,525 (+)NCBI
GRCh371256,391,043 - 56,399,309 (+)ENTREZGENE
Build 361254,677,310 - 54,685,576 (+)NCBI Archive
HuRef1253,429,929 - 53,438,195 (+)ENTREZGENE
CHM1_11256,358,154 - 56,366,418 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001032387   ⟹   NP_001027559
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381255,997,276 - 56,005,525 (+)NCBI
GRCh371256,391,043 - 56,399,309 (+)ENTREZGENE
Build 361254,677,310 - 54,685,576 (+)NCBI Archive
HuRef1253,429,929 - 53,438,195 (+)ENTREZGENE
CHM1_11256,358,154 - 56,366,418 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019905   ⟹   XP_016875394
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381255,992,547 - 56,005,525 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019906   ⟹   XP_016875395
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,000,636 - 56,005,525 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019907   ⟹   XP_016875396
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381255,992,547 - 56,005,525 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019908   ⟹   XP_016875397
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381256,000,632 - 56,005,525 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024449167   ⟹   XP_024304935
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381255,992,547 - 56,005,525 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_000447   ⟸   NM_000456
- UniProtKB: P51687 (UniProtKB/Swiss-Prot),   A0A024RB79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001027558   ⟸   NM_001032386
- UniProtKB: P51687 (UniProtKB/Swiss-Prot),   A0A024RB79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001027559   ⟸   NM_001032387
- UniProtKB: P51687 (UniProtKB/Swiss-Prot),   A0A024RB79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016875396   ⟸   XM_017019907
- Peptide Label: isoform X2
- UniProtKB: P51687 (UniProtKB/Swiss-Prot),   A0A024RB79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016875394   ⟸   XM_017019905
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016875397   ⟸   XM_017019908
- Peptide Label: isoform X2
- UniProtKB: P51687 (UniProtKB/Swiss-Prot),   A0A024RB79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016875395   ⟸   XM_017019906
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024304935   ⟸   XM_024449167
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000266971   ⟸   ENST00000266971
RefSeq Acc Id: ENSP00000449872   ⟸   ENST00000546833
RefSeq Acc Id: ENSP00000448637   ⟸   ENST00000547586
RefSeq Acc Id: ENSP00000450245   ⟸   ENST00000548274
RefSeq Acc Id: ENSP00000450264   ⟸   ENST00000550065
RefSeq Acc Id: ENSP00000377668   ⟸   ENST00000394109
RefSeq Acc Id: ENSP00000377674   ⟸   ENST00000394115
RefSeq Acc Id: ENSP00000449443   ⟸   ENST00000551841
RefSeq Acc Id: ENSP00000450049   ⟸   ENST00000552258
RefSeq Acc Id: ENSP00000348440   ⟸   ENST00000356124
Protein Domains
Cytochrome b5 heme-binding

Promoters
RGD ID:6790524
Promoter ID:HG_KWN:15872
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_000456,   NM_001032386,   NM_001032387,   UC009ZOH.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361254,676,436 - 54,677,547 (+)MPROMDB
RGD ID:7224351
Promoter ID:EPDNEW_H17921
Type:single initiation site
Name:SUOX_2
Description:sulfite oxidase
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H17922  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381255,996,914 - 55,996,974EPDNEW
RGD ID:7224353
Promoter ID:EPDNEW_H17922
Type:initiation region
Name:SUOX_1
Description:sulfite oxidase
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H17921  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381255,997,286 - 55,997,346EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001032386.2(SUOX):c.650G>A (p.Arg217Gln) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000698394] Chr12:56004039 [GRCh38]
Chr12:56397823 [GRCh37]
Chr12:12q13.2
pathogenic|likely pathogenic
NM_001032386.2(SUOX):c.794C>A (p.Ala265Asp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000758700] Chr12:56004183 [GRCh38]
Chr12:56397967 [GRCh37]
Chr12:12q13.2
pathogenic
S370Y single nucleotide variant Isolated sulfite oxidase deficiency [RCV000004026] Chr12 pathogenic
NM_001032386.2(SUOX):c.1589G>A (p.Gly530Asp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000758702] Chr12:56004978 [GRCh38]
Chr12:56398762 [GRCh37]
Chr12:12q13.2
pathogenic
SUOX, 1-BP DEL, 1244G deletion Isolated sulfite oxidase deficiency [RCV000004028] Chr12 pathogenic
NM_001032386.2(SUOX):c.193G>A (p.Gly65Ser) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001302560] Chr12:56002685 [GRCh38]
Chr12:56396469 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1281G>C (p.Ser427=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000363638]|not specified [RCV000118423] Chr12:56004670 [GRCh38]
Chr12:56398454 [GRCh37]
Chr12:12q13.2
benign|likely benign|conflicting interpretations of pathogenicity
NM_001032386.2(SUOX):c.475G>T (p.Glu159Ter) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001293327] Chr12:56003864 [GRCh38]
Chr12:56397648 [GRCh37]
Chr12:12q13.2
likely pathogenic
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33
pathogenic
GRCh38/hg38 12q13.13-13.3(chr12:53420606-56202942)x3 copy number gain See cases [RCV000141435] Chr12:53420606..56202942 [GRCh38]
Chr12:53814390..56596726 [GRCh37]
Chr12:52100657..54882993 [NCBI36]
Chr12:12q13.13-13.3
pathogenic
NM_001032386.2(SUOX):c.1358G>A (p.Gly453Asp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000383805]|not specified [RCV000194521] Chr12:56004747 [GRCh38]
Chr12:56398531 [GRCh37]
Chr12:12q13.2
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001032386.2(SUOX):c.332T>A (p.Val111Asp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000184031] Chr12:56003721 [GRCh38]
Chr12:56397505 [GRCh37]
Chr12:12q13.2
likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic|likely pathogenic
NM_001032386.2(SUOX):c.842_843del (p.Leu281fs) deletion Inborn genetic diseases [RCV001267499]|not provided [RCV000756731] Chr12:56004231..56004232 [GRCh38]
Chr12:56398015..56398016 [GRCh37]
Chr12:12q13.2
pathogenic|likely pathogenic
NM_001032386.2(SUOX):c.739C>A (p.Leu247Met) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001248746]|not provided [RCV000756732] Chr12:56004128 [GRCh38]
Chr12:56397912 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1335C>T (p.Ile445=) single nucleotide variant not provided [RCV000756733] Chr12:56004724 [GRCh38]
Chr12:56398508 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.1298G>A (p.Arg433Gln) single nucleotide variant not provided [RCV000380532] Chr12:56004687 [GRCh38]
Chr12:56398471 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_000456.2(SUOX):c.-322C>T single nucleotide variant Isolated sulfite oxidase deficiency [RCV000319885] Chr12:55997263 [GRCh38]
Chr12:56391047 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.-32C>T single nucleotide variant Isolated sulfite oxidase deficiency [RCV000321062] Chr12:55997702 [GRCh38]
Chr12:56391486 [GRCh37]
Chr12:12q13.2
benign|likely benign
NM_001032386.2(SUOX):c.1247C>T (p.Ser416Phe) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000322978] Chr12:56004636 [GRCh38]
Chr12:56398420 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.-11+1613C>T single nucleotide variant Isolated sulfite oxidase deficiency [RCV000326707] Chr12:55999336 [GRCh38]
Chr12:56393120 [GRCh37]
Chr12:12q13.2
likely benign|uncertain significance
NM_001032386.2(SUOX):c.1282G>A (p.Ala428Thr) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000328752] Chr12:56004671 [GRCh38]
Chr12:56398455 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.*26C>G single nucleotide variant Isolated sulfite oxidase deficiency [RCV000330432] Chr12:56005053 [GRCh38]
Chr12:56398837 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.*355T>C single nucleotide variant Isolated sulfite oxidase deficiency [RCV000336067] Chr12:56005382 [GRCh38]
Chr12:56399166 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.23T>C (p.Val8Ala) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000349790] Chr12:56002244 [GRCh38]
Chr12:56396028 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.228G>T (p.Arg76Ser) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000351081] Chr12:56002720 [GRCh38]
Chr12:56396504 [GRCh37]
Chr12:12q13.2
benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001032386.2(SUOX):c.983C>T (p.Thr328Ile) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000357593] Chr12:56004372 [GRCh38]
Chr12:56398156 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.-85G>A single nucleotide variant Isolated sulfite oxidase deficiency [RCV000356050] Chr12:55997649 [GRCh38]
Chr12:56391433 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.507C>T (p.Thr169=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000356881] Chr12:56003896 [GRCh38]
Chr12:56397680 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_000456.2(SUOX):c.-326A>T single nucleotide variant Isolated sulfite oxidase deficiency [RCV000260145] Chr12:55997259 [GRCh38]
Chr12:56391043 [GRCh37]
Chr12:12q13.2
likely benign|uncertain significance
NM_001032386.2(SUOX):c.-25G>C single nucleotide variant Isolated sulfite oxidase deficiency [RCV000380161] Chr12:55997709 [GRCh38]
Chr12:56391493 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.-11+1672T>A single nucleotide variant Isolated sulfite oxidase deficiency [RCV000381379] Chr12:55999395 [GRCh38]
Chr12:56393179 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.-58C>A single nucleotide variant Isolated sulfite oxidase deficiency [RCV000266006] Chr12:55997676 [GRCh38]
Chr12:56391460 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1050T>C (p.Tyr350=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000267934] Chr12:56004439 [GRCh38]
Chr12:56398223 [GRCh37]
Chr12:12q13.2
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001032386.2(SUOX):c.1281G>T (p.Ser427=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000268966] Chr12:56004670 [GRCh38]
Chr12:56398454 [GRCh37]
Chr12:12q13.2
benign|likely benign
NM_001032386.2(SUOX):c.*155C>T single nucleotide variant Isolated sulfite oxidase deficiency [RCV000389617] Chr12:56005182 [GRCh38]
Chr12:56398966 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.279C>T (p.His93=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000392392] Chr12:56003668 [GRCh38]
Chr12:56397452 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.50+9G>A single nucleotide variant Isolated sulfite oxidase deficiency [RCV000392410] Chr12:56002280 [GRCh38]
Chr12:56396064 [GRCh37]
Chr12:12q13.2
likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001032386.2(SUOX):c.*496T>C single nucleotide variant Isolated sulfite oxidase deficiency [RCV000401231] Chr12:56005523 [GRCh38]
Chr12:56399307 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.629C>T (p.Pro210Leu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000403618] Chr12:56004018 [GRCh38]
Chr12:56397802 [GRCh37]
Chr12:12q13.2
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001032386.2(SUOX):c.-11+1604T>G single nucleotide variant Isolated sulfite oxidase deficiency [RCV000285737] Chr12:55999327 [GRCh38]
Chr12:56393111 [GRCh37]
Chr12:12q13.2
likely benign|uncertain significance
NM_001032386.2(SUOX):c.-11+1723G>A single nucleotide variant Isolated sulfite oxidase deficiency [RCV000290183] Chr12:55999446 [GRCh38]
Chr12:56393230 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1586G>A (p.Arg529Gln) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000294067] Chr12:56004975 [GRCh38]
Chr12:56398759 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.*187G>T single nucleotide variant Isolated sulfite oxidase deficiency [RCV000295081] Chr12:56005214 [GRCh38]
Chr12:56398998 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.192C>T (p.Leu64=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000295988] Chr12:56002684 [GRCh38]
Chr12:56396468 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.364C>G (p.Pro122Ala) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000297402] Chr12:56003753 [GRCh38]
Chr12:56397537 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.889C>T (p.Arg297Trp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000302757] Chr12:56004278 [GRCh38]
Chr12:56398062 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.968C>T (p.Ser323Leu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000797734]|not provided [RCV000732664] Chr12:56004357 [GRCh38]
Chr12:56398141 [GRCh37]
Chr12:12q13.2
uncertain significance
GRCh37/hg19 12q13.2(chr12:55975308-56593032)x3 copy number gain See cases [RCV000446219] Chr12:55975308..56593032 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1306G>A (p.Glu436Lys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000800617]|not provided [RCV000423314] Chr12:56004695 [GRCh38]
Chr12:56398479 [GRCh37]
Chr12:12q13.2
uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
NM_001032386.2(SUOX):c.98del (p.Asn33fs) deletion Isolated sulfite oxidase deficiency [RCV000634925] Chr12:56002588 [GRCh38]
Chr12:56396372 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.363dup (p.Pro122fs) duplication Isolated sulfite oxidase deficiency [RCV000634924] Chr12:56003746..56003747 [GRCh38]
Chr12:56397530..56397531 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.931G>A (p.Glu311Lys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000698858] Chr12:56004320 [GRCh38]
Chr12:56398104 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.186A>T (p.Leu62Phe) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000688935] Chr12:56002678 [GRCh38]
Chr12:56396462 [GRCh37]
Chr12:12q13.2
uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
NM_001032386.2(SUOX):c.596C>T (p.Pro199Leu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000914385] Chr12:56003985 [GRCh38]
Chr12:56397769 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.1388C>T (p.Ser463Phe) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000761535] Chr12:56004777 [GRCh38]
Chr12:56398561 [GRCh37]
Chr12:12q13.2
pathogenic|likely pathogenic
NM_001032386.2(SUOX):c.1280_1281delinsAC (p.Ser427Tyr) indel Isolated sulfite oxidase deficiency [RCV000761554] Chr12:56004669..56004670 [GRCh38]
Chr12:56398453..56398454 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.796G>A (p.Gly266Ser) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000988862]|not specified [RCV001175544] Chr12:56004185 [GRCh38]
Chr12:56397969 [GRCh37]
Chr12:12q13.2
likely pathogenic|uncertain significance
NM_001032386.2(SUOX):c.1126C>T (p.Arg376Cys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000988863] Chr12:56004515 [GRCh38]
Chr12:56398299 [GRCh37]
Chr12:12q13.2
likely pathogenic
NM_001032386.2(SUOX):c.-107C>T single nucleotide variant Isolated sulfite oxidase deficiency [RCV001114422] Chr12:55997627 [GRCh38]
Chr12:56391411 [GRCh37]
Chr12:12q13.2
benign
NM_001032386.2(SUOX):c.1636T>A (p.Ter546Arg) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001509709]|not provided [RCV000904609] Chr12:56005025 [GRCh38]
Chr12:56398809 [GRCh37]
Chr12:12q13.2
benign
NM_001032386.2(SUOX):c.177G>C (p.Gly59=) single nucleotide variant not provided [RCV000975983] Chr12:56002669 [GRCh38]
Chr12:56396453 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.19G>A (p.Ala7Thr) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001470153]|not provided [RCV000902979] Chr12:56002240 [GRCh38]
Chr12:56396024 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.977C>A (p.Thr326Asn) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000897728] Chr12:56004366 [GRCh38]
Chr12:56398150 [GRCh37]
Chr12:12q13.2
benign
NM_001032386.2(SUOX):c.199G>C (p.Val67Leu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001037373] Chr12:56002691 [GRCh38]
Chr12:56396475 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1200C>G (p.Tyr400Ter) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000758701] Chr12:56004589 [GRCh38]
Chr12:56398373 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.1035G>A (p.Glu345=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001475108]|not provided [RCV000930331] Chr12:56004424 [GRCh38]
Chr12:56398208 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.520del (p.Asp174fs) deletion Isolated sulfite oxidase deficiency [RCV000758699] Chr12:56003909 [GRCh38]
Chr12:56397693 [GRCh37]
Chr12:12q13.2
pathogenic|likely pathogenic
NM_001032386.2(SUOX):c.1333A>G (p.Ile445Val) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000806533] Chr12:56004722 [GRCh38]
Chr12:56398506 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1390_1391del (p.Leu464fs) microsatellite Isolated sulfite oxidase deficiency [RCV000805760] Chr12:56004776..56004777 [GRCh38]
Chr12:56398560..56398561 [GRCh37]
Chr12:12q13.2
conflicting interpretations of pathogenicity|uncertain significance
NM_001032386.2(SUOX):c.1376G>A (p.Arg459Gln) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000791011] Chr12:56004765 [GRCh38]
Chr12:56398549 [GRCh37]
Chr12:12q13.2
likely pathogenic
NM_001032386.2(SUOX):c.1137A>G (p.Lys379=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001114506] Chr12:56004526 [GRCh38]
Chr12:56398310 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.119G>A (p.Arg40His) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000799285] Chr12:56002611 [GRCh38]
Chr12:56396395 [GRCh37]
Chr12:12q13.2
conflicting interpretations of pathogenicity|uncertain significance
NM_001032386.2(SUOX):c.228+1G>A single nucleotide variant Isolated sulfite oxidase deficiency [RCV001061722] Chr12:56002721 [GRCh38]
Chr12:56396505 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1040T>C (p.Leu347Pro) single nucleotide variant not specified [RCV001175543] Chr12:56004429 [GRCh38]
Chr12:56398213 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1313_1316del (p.Val438fs) deletion Isolated sulfite oxidase deficiency [RCV001208096] Chr12:56004702..56004705 [GRCh38]
Chr12:56398486..56398489 [GRCh37]
Chr12:12q13.2
likely pathogenic
NM_001032386.2(SUOX):c.599C>T (p.Pro200Leu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001196618] Chr12:56003988 [GRCh38]
Chr12:56397772 [GRCh37]
Chr12:12q13.2
likely pathogenic
NM_001032386.2(SUOX):c.1534G>T (p.Asp512Tyr) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000988864] Chr12:56004923 [GRCh38]
Chr12:56398707 [GRCh37]
Chr12:12q13.2
likely pathogenic|conflicting interpretations of pathogenicity
NM_001032386.2(SUOX):c.1612C>T (p.Arg538Cys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001110469] Chr12:56005001 [GRCh38]
Chr12:56398785 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.*47A>C single nucleotide variant Isolated sulfite oxidase deficiency [RCV001110470] Chr12:56005074 [GRCh38]
Chr12:56398858 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.89G>C (p.Cys30Ser) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001111124] Chr12:56002581 [GRCh38]
Chr12:56396365 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.*369G>A single nucleotide variant Isolated sulfite oxidase deficiency [RCV001111225] Chr12:56005396 [GRCh38]
Chr12:56399180 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.*479T>C single nucleotide variant Isolated sulfite oxidase deficiency [RCV001111226] Chr12:56005506 [GRCh38]
Chr12:56399290 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1297C>T (p.Arg433Trp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000972279] Chr12:56004686 [GRCh38]
Chr12:56398470 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.485C>T (p.Pro162Leu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001230901] Chr12:56003874 [GRCh38]
Chr12:56397658 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.713C>T (p.Pro238Leu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001113128] Chr12:56004102 [GRCh38]
Chr12:56397886 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1527G>A (p.Lys509=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001065821] Chr12:56004916 [GRCh38]
Chr12:56398700 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.574C>T (p.Arg192Trp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV000912733] Chr12:56003963 [GRCh38]
Chr12:56397747 [GRCh37]
Chr12:12q13.2
likely benign|conflicting interpretations of pathogenicity
NM_001032386.2(SUOX):c.1243G>A (p.Asp415Asn) single nucleotide variant not provided [RCV001092485] Chr12:56004632 [GRCh38]
Chr12:56398416 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.*311A>G single nucleotide variant Isolated sulfite oxidase deficiency [RCV001110471] Chr12:56005338 [GRCh38]
Chr12:56399122 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.51-14G>A single nucleotide variant Isolated sulfite oxidase deficiency [RCV001111123] Chr12:56002529 [GRCh38]
Chr12:56396313 [GRCh37]
Chr12:12q13.2
uncertain significance
NC_000012.12:g.56005531G>C single nucleotide variant Isolated sulfite oxidase deficiency [RCV001111227] Chr12:56005531 [GRCh38]
Chr12:56399315 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.890G>A (p.Arg297Gln) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001069660] Chr12:56004279 [GRCh38]
Chr12:56398063 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.621C>T (p.Tyr207=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001113127] Chr12:56004010 [GRCh38]
Chr12:56397794 [GRCh37]
Chr12:12q13.2
conflicting interpretations of pathogenicity|uncertain significance
NM_001032386.2(SUOX):c.769G>A (p.Glu257Lys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001230902] Chr12:56004158 [GRCh38]
Chr12:56397942 [GRCh37]
Chr12:12q13.2
uncertain significance
GRCh37/hg19 12q13.2-14.1(chr12:55552371-62126304)x3 copy number gain not provided [RCV001006505] Chr12:55552371..62126304 [GRCh37]
Chr12:12q13.2-14.1
pathogenic
NM_001032386.2(SUOX):c.-129A>G single nucleotide variant Isolated sulfite oxidase deficiency [RCV001114421] Chr12:55997330 [GRCh38]
Chr12:56391114 [GRCh37]
Chr12:12q13.2
uncertain significance
GRCh37/hg19 12q13.2(chr12:56333246-56558418)x3 copy number gain not provided [RCV001259615] Chr12:56333246..56558418 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.649C>T (p.Arg217Trp) single nucleotide variant Inborn genetic diseases [RCV001266711] Chr12:56004038 [GRCh38]
Chr12:56397822 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.810dup (p.Glu271Ter) duplication Isolated sulfite oxidase deficiency [RCV001257120] Chr12:56004198..56004199 [GRCh38]
Chr12:56397982..56397983 [GRCh37]
Chr12:12q13.2
likely pathogenic
NM_001032386.2(SUOX):c.545G>A (p.Arg182His) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001294531] Chr12:56003934 [GRCh38]
Chr12:56397718 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1573A>G (p.Ile525Val) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001349582] Chr12:56004962 [GRCh38]
Chr12:56398746 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1097G>A (p.Arg366His) single nucleotide variant not provided [RCV001268179] Chr12:56004486 [GRCh38]
Chr12:56398270 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.1480A>G (p.Lys494Glu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001332470] Chr12:56004869 [GRCh38]
Chr12:56398653 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.544C>T (p.Arg182Cys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001296257] Chr12:56003933 [GRCh38]
Chr12:56397717 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1625A>G (p.Tyr542Cys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001305164] Chr12:56005014 [GRCh38]
Chr12:56398798 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1084G>A (p.Gly362Ser) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001280525] Chr12:56004473 [GRCh38]
Chr12:56398257 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.1612C>G (p.Arg538Gly) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001341635] Chr12:56005001 [GRCh38]
Chr12:56398785 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.672C>G (p.Asn224Lys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001326751] Chr12:56004061 [GRCh38]
Chr12:56397845 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1327G>T (p.Val443Leu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001352303] Chr12:56004716 [GRCh38]
Chr12:56398500 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1487C>G (p.Pro496Arg) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001318213] Chr12:56004876 [GRCh38]
Chr12:56398660 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.823G>A (p.Val275Ile) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001318214] Chr12:56004212 [GRCh38]
Chr12:56397996 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.424G>A (p.Val142Ile) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001320863] Chr12:56003813 [GRCh38]
Chr12:56397597 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1501C>A (p.Gln501Lys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001342868] Chr12:56004890 [GRCh38]
Chr12:56398674 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.221G>A (p.Arg74Gln) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001338214] Chr12:56002713 [GRCh38]
Chr12:56396497 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.874C>T (p.Arg292Cys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001374276] Chr12:56004263 [GRCh38]
Chr12:56398047 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.699C>T (p.His233=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001414854] Chr12:56004088 [GRCh38]
Chr12:56397872 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.1083C>T (p.His361=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001422499] Chr12:56004472 [GRCh38]
Chr12:56398256 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.575G>A (p.Arg192Gln) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001369628] Chr12:56003964 [GRCh38]
Chr12:56397748 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.595C>G (p.Pro199Ala) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001373561] Chr12:56003984 [GRCh38]
Chr12:56397768 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1442G>A (p.Arg481His) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001296996] Chr12:56004831 [GRCh38]
Chr12:56398615 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1016C>T (p.Ala339Val) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001299897] Chr12:56004405 [GRCh38]
Chr12:56398189 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1093G>A (p.Val365Met) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001321504] Chr12:56004482 [GRCh38]
Chr12:56398266 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1175A>G (p.Tyr392Cys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001322852] Chr12:56004564 [GRCh38]
Chr12:56398348 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.140G>A (p.Gly47Asp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001360310] Chr12:56002632 [GRCh38]
Chr12:56396416 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.61A>G (p.Ile21Val) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001299248] Chr12:56002553 [GRCh38]
Chr12:56396337 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1583T>C (p.Leu528Pro) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001346780] Chr12:56004972 [GRCh38]
Chr12:56398756 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1441C>T (p.Arg481Cys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001326607] Chr12:56004830 [GRCh38]
Chr12:56398614 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.822G>C (p.Gln274His) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001270791] Chr12:56004211 [GRCh38]
Chr12:56397995 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1012C>T (p.Arg338Trp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001347604]|not provided [RCV001357184] Chr12:56004401 [GRCh38]
Chr12:56398185 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1192C>T (p.Arg398Trp) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001317347] Chr12:56004581 [GRCh38]
Chr12:56398365 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.496G>A (p.Val166Ile) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001364340] Chr12:56003885 [GRCh38]
Chr12:56397669 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.514A>G (p.Thr172Ala) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001367551] Chr12:56003903 [GRCh38]
Chr12:56397687 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1521_1524del (p.Cys508fs) microsatellite Isolated sulfite oxidase deficiency [RCV001270364] Chr12:56004906..56004909 [GRCh38]
Chr12:56398690..56398693 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.941C>G (p.Ala314Gly) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001340892] Chr12:56004330 [GRCh38]
Chr12:56398114 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1201A>G (p.Lys401Glu) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001293328] Chr12:56004590 [GRCh38]
Chr12:56398374 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.793G>A (p.Ala265Thr) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001371682] Chr12:56004182 [GRCh38]
Chr12:56397966 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.691C>T (p.Arg231Cys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001316243] Chr12:56004080 [GRCh38]
Chr12:56397864 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.40C>A (p.Gln14Lys) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001303388] Chr12:56002261 [GRCh38]
Chr12:56396045 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.1162C>A (p.Pro388Thr) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001307965] Chr12:56004551 [GRCh38]
Chr12:56398335 [GRCh37]
Chr12:12q13.2
uncertain significance
NM_001032386.2(SUOX):c.627A>G (p.Thr209=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001467870] Chr12:56004016 [GRCh38]
Chr12:56397800 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.1515C>T (p.Asn505=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001430697] Chr12:56004904 [GRCh38]
Chr12:56398688 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.1119G>A (p.Val373=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001423375] Chr12:56004508 [GRCh38]
Chr12:56398292 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.600T>C (p.Pro200=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001437967] Chr12:56003989 [GRCh38]
Chr12:56397773 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.1032T>G (p.Ala344=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001445179] Chr12:56004421 [GRCh38]
Chr12:56398205 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.621C>G (p.Tyr207Ter) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001383710] Chr12:56004010 [GRCh38]
Chr12:56397794 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.1095G>A (p.Val365=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001467852] Chr12:56004484 [GRCh38]
Chr12:56398268 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.1632C>T (p.Ser544=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001400898] Chr12:56005021 [GRCh38]
Chr12:56398805 [GRCh37]
Chr12:12q13.2
likely benign
NM_001032386.2(SUOX):c.115C>T (p.Gln39Ter) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001380599] Chr12:56002607 [GRCh38]
Chr12:56396391 [GRCh37]
Chr12:12q13.2
pathogenic
NM_001032386.2(SUOX):c.681A>G (p.Pro227=) single nucleotide variant Isolated sulfite oxidase deficiency [RCV001456462] Chr12:56004070 [GRCh38]
Chr12:56397854 [GRCh37]
Chr12:12q13.2
likely benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11460 AgrOrtholog
COSMIC SUOX COSMIC
Ensembl Genes ENSG00000139531 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000266971 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000348440 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000377668 UniProtKB/Swiss-Prot
  ENSP00000377674 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000448637 UniProtKB/TrEMBL
  ENSP00000449443 UniProtKB/TrEMBL
  ENSP00000449872 UniProtKB/TrEMBL
  ENSP00000450049 UniProtKB/TrEMBL
  ENSP00000450245 UniProtKB/Swiss-Prot
  ENSP00000450264 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000266971 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000356124 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000394109 UniProtKB/Swiss-Prot
  ENST00000394115 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000546833 UniProtKB/TrEMBL
  ENST00000547586 UniProtKB/TrEMBL
  ENST00000548274 UniProtKB/Swiss-Prot
  ENST00000550065 UniProtKB/Swiss-Prot
  ENST00000551841 UniProtKB/TrEMBL
  ENST00000552258 UniProtKB/TrEMBL
Gene3D-CATH 3.10.120.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.90.420.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000139531 GTEx
HGNC ID HGNC:11460 ENTREZGENE
Human Proteome Map SUOX Human Proteome Map
InterPro Cyt_B5-like_heme/steroid-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_B5-like_heme/steroid_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_B5_heme-BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_E-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MoCF_OxRdtse_dimer UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Mopterin_OxRdtase_euk UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OxRdtase_Mopterin-bd_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OxRdtase_Mopterin-bd_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OxRdtase_Mopterin_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6821 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 6821 ENTREZGENE
OMIM 272300 OMIM
  606887 OMIM
Pfam Cyt-b5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Mo-co_dimer UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Oxidored_molyb UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36250 PharmGKB
PRINTS CYTOCHROMEB5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EUMOPTERIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE CYTOCHROME_B5_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CYTOCHROME_B5_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MOLYBDOPTERIN_EUK UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Cyt-b5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF55856 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF56524 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF81296 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024RB79 ENTREZGENE, UniProtKB/TrEMBL
  D6QX84_HUMAN UniProtKB/TrEMBL
  F8VPA2_HUMAN UniProtKB/TrEMBL
  F8VRK9_HUMAN UniProtKB/TrEMBL
  F8VVW9_HUMAN UniProtKB/TrEMBL
  F8VX56_HUMAN UniProtKB/TrEMBL
  L8E787_HUMAN UniProtKB/TrEMBL
  P51687 ENTREZGENE, UniProtKB/Swiss-Prot