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MitoProteome Human Mitochondrial Protein Database
MitoProteome Database
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Related Proteins
MT000159
Gene Information
Entrez Gene ID
1528
Gene Name
cytochrome b5 type A (microsomal)
Gene Symbol
CYB5A
Species
Homo sapiens
Gene Ontology (GO Annotations)
GO ID
Source
Type
Description
GO:0005783
IEA:UniProtKB-KW
C
endoplasmic reticulum
GO:0070062
IDA:UniProt
C
extracellular vesicular exosome
GO:0016021
IEA:UniProtKB-KW
C
integral component of membrane
GO:0016020
IDA:UniProtKB
C
membrane
GO:0005741
TAS:Reactome
C
mitochondrial outer membrane
GO:0004033
TAS:Reactome
F
aldo-keto reductase (NADP) activity
GO:0004129
TAS:ProtInc
F
cytochrome-c oxidase activity
GO:0019899
IPI:BHF-UCL
F
enzyme binding
GO:0020037
IEA:InterPro
F
heme binding
GO:0046872
IEA:UniProtKB-KW
F
metal ion binding
GO:1902600
TAS:GOC
P
hydrogen ion transmembrane transport
GO:0019852
TAS:Reactome
P
L-ascorbic acid metabolic process
GO:0044281
TAS:Reactome
P
small molecule metabolic process
GO:0006766
TAS:Reactome
P
vitamin metabolic process
GO:0006767
TAS:Reactome
P
water-soluble vitamin metabolic process
REACTOME Pathway Links
REACTOME Pathway ID
Description
REACT_169280
Defective AMN causes hereditary megaloblastic anemia 1
REACT_169403
Defective BTD causes biotidinase deficiency
REACT_169178
Defective CD320 causes methylmalonic aciduria
REACT_169132
Defective CUBN causes hereditary megaloblastic anemia 1
REACT_169415
Defective GIF causes intrinsic factor deficiency
REACT_169312
Defective HLCS causes multiple carboxylase deficiency
REACT_169363
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
REACT_169316
Defective MMAA causes methylmalonic aciduria type cblA
REACT_169318
Defective MMAB causes methylmalonic aciduria type cblB
REACT_169169
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
REACT_169256
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
REACT_169149
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
REACT_169439
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
REACT_169313
Defective MUT causes methylmalonic aciduria mut type
REACT_169120
Defective TCN2 causes hereditary megaloblastic anemia
REACT_169238
Defects in biotin (Btn) metabolism
REACT_169429
Defects in cobalamin (B12) metabolism
REACT_169385
Defects in vitamin and cofactor metabolism
REACT_116125
Disease
REACT_111217
Metabolism
REACT_11193
Metabolism of vitamins and cofactors
REACT_11238
Metabolism of water-soluble vitamins and cofactors
REACT_11202
Vitamin C (ascorbate) metabolism
MitoProteome Human Mitochondrial Protein Database
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