HCSGD entry for CYB5R3


1. General information

Official gene symbolCYB5R3
Entrez ID1727
Gene full namecytochrome b5 reductase 3
Other gene symbolsB5R DIA1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0004128Cytochrome-b5 reductase activity, acting on NAD(P)HTASmolecular_function
GO:0005737CytoplasmTAScellular_component
GO:0005741Mitochondrial outer membraneTAScellular_component
GO:0005743Mitochondrial inner membraneIEAcellular_component
GO:0005783Endoplasmic reticulumIDAcellular_component
GO:0005789Endoplasmic reticulum membraneIEAcellular_component
GO:0005811Lipid particleIDAcellular_component
GO:0005833Hemoglobin complexTAScellular_component
GO:0006695Cholesterol biosynthetic processIEAbiological_process
GO:0006766Vitamin metabolic processTASbiological_process
GO:0006767Water-soluble vitamin metabolic processTASbiological_process
GO:0008015Blood circulationTASbiological_process
GO:0016020MembraneTAScellular_component
GO:0016208AMP bindingIEAmolecular_function
GO:0016491Oxidoreductase activityIEAmolecular_function
GO:0019852L-ascorbic acid metabolic processTASbiological_process
GO:0043531ADP bindingIEAmolecular_function
GO:0044281Small molecule metabolic processTASbiological_process
GO:0050660Flavin adenine dinucleotide bindingIEAmolecular_function
GO:0051287NAD bindingIEAmolecular_function
GO:0071949FAD bindingIDAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.19953766190.21644299610.86208826520.8958355031

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Down-0.1519499143
GSE13712_SHEARDown-0.1715993983
GSE13712_STATICDown-0.1642618205
GSE19018Up0.4783485861
GSE19899_A1Down-0.5618359878
GSE19899_A2Up0.3726054834
PubMed_21979375_A1Up0.5292352846
PubMed_21979375_A2Down-1.0420326038
GSE35957Up0.1737381918
GSE36640Up0.8980521801
GSE54402Down-0.2877640876
GSE9593Up0.7216759125
GSE43922Down-0.2074971759
GSE24585Up0.0410369871
GSE37065Up0.0402906442
GSE28863_A1Down-0.0989099740
GSE28863_A2Down-0.2056932848
GSE28863_A3Up0.1317125771
GSE28863_A4Down-0.0486328165
GSE48662Up0.5614328844

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

NADHDB00157 NUTR00041 | DB01907 | EXPT02287 | DB03527

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-98-5pMIMAT0000096MIRT027454MicroarrayFunctional MTI (Weak)19088304
hsa-miR-744-5pMIMAT0004945MIRT037551CLASHFunctional MTI (Weak)23622248
hsa-miR-484MIMAT0002174MIRT042354CLASHFunctional MTI (Weak)23622248
hsa-miR-378a-3pMIMAT0000732MIRT043904CLASHFunctional MTI (Weak)23622248
hsa-miR-92a-3pMIMAT0000092MIRT049610CLASHFunctional MTI (Weak)23622248
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    • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

24450884AIMS: Membrane-bound CYB5R3 deficiency in humans causes recessive hereditary methaemoglobinaemia (RHM), an incurable disease that is characterized by severe neurological disorders
24450884CYB5R3 encodes for NADH-dependent redox enzyme that contributes to metabolic homeostasis and stress protection; however, how it is involved in the neurological pathology of RHM remains unknown
24450884Here, the role and transcriptional regulation of CYB5R3 was studied under nutritional and oxidative stress
24450884INNOVATION: Our findings demonstrate that CYB5R3 contributes to regulate redox homeostasis, aerobic metabolism, and cellular senescence, suggesting that CYB5R3 might be a key effector of oxidative and nutritional stress pathways
24450884These results unveil a potential mechanism of action by which CYB5R3 deficiency contributes to the pathophysiological underpinnings of neurological disorders in RHM patients
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