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CYB5R3
Gene Name
cytochrome b5 reductase 3
Image
Gene Ontology Annotations
Cellular Component
Cytoplasm
Mitochondrion
Mitochondrial Outer Membrane
Mitochondrial Inner Membrane
Endoplasmic Reticulum
Endoplasmic Reticulum Membrane
Lipid Particle
Hemoglobin Complex
Membrane
Extracellular Vesicular Exosome
Molecular Function
Cytochrome-b5 Reductase Activity, Acting On NAD(P)H
AMP Binding
ADP Binding
Flavin Adenine Dinucleotide Binding
NAD Binding
FAD Binding
Biological Process
Cholesterol Biosynthetic Process
Vitamin Metabolic Process
Water-soluble Vitamin Metabolic Process
Blood Circulation
L-ascorbic Acid Metabolic Process
Small Molecule Metabolic Process
Oxidation-reduction Process
Pathways
Metabolism of vitamins and cofactors
Defective CD320 causes methylmalonic aciduria
Defective GIF causes intrinsic factor deficiency
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
Defective HLCS causes multiple carboxylase deficiency
Defective MMAB causes methylmalonic aciduria type cblB
Defective BTD causes biotidinase deficiency
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
Vitamin C (ascorbate) metabolism
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
Defective MMAA causes methylmalonic aciduria type cblA
Defective CUBN causes hereditary megaloblastic anemia 1
Defective AMN causes hereditary megaloblastic anemia 1
Defective MUT causes methylmalonic aciduria mut type
Metabolism of water-soluble vitamins and cofactors
Defects in biotin (Btn) metabolism
Defective TCN2 causes hereditary megaloblastic anemia
Defects in cobalamin (B12) metabolism
Defects in vitamin and cofactor metabolism
Drugs
NADH
Nicotinamide-Adenine-Dinucleotide
Flavin-Adenine Dinucleotide
Diseases
GWAS
Protein-protein Interactions
4 interactors:
CYB5A
CYCS
HBG2
SPP1
Entrez ID
1727
HPRD ID
08942
Ensembl ID
ENSG00000100243
Uniprot IDs
P00387
PDB IDs
1M91
1UMK
Enriched GO Terms of Interacting Partners
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Negative Regulation Of Collateral Sprouting Of Intact Axon In Response To Injury
Regulation Of Collateral Sprouting Of Intact Axon In Response To Injury
Mitochondrial Electron Transport, Cytochrome C To Oxygen
Negative Regulation Of Collateral Sprouting
Negative Regulation Of Axon Regeneration
Mitochondrial Electron Transport, Ubiquinol To Cytochrome C
L-ascorbic Acid Metabolic Process
Activation Of Cysteine-type Endopeptidase Activity Involved In Apoptotic Process By Cytochrome C
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