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Gene id 4705
Gene Summary    Protein Summary    Gene ontology    KEGG pathways    Diseases    PubMed    

Gene Summary

Gene Symbol NDUFA10   Gene   UCSC   Ensembl
Aliases CI-42KD, CI-42k, MC1DN22
Gene name NADH:ubiquinone oxidoreductase subunit A10
Alternate names NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial, NADH-ubiquinone oxidoreductase 42 kDa subunit, complex I 42kDa subunit,
Gene location 2q37.3 (240025401: 239892441)     Exons: 16     NC_000002.12
Gene summary(Entrez) The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to th

Protein Summary

Protein general information O95299  

Name: NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial (Complex I 42kD) (CI 42kD) (NADH ubiquinone oxidoreductase 42 kDa subunit)

Length: 355  Mass: 40751

Sequence MALRLLKLAATSASARVVAAGAQRVRGIHSSVQCKLRYGMWHFLLGDKASKRLTERSRVITVDGNICTGKGKLAK
EIAEKLGFKHFPEAGIHYPDSTTGDGKPLATDYNGNCSLEKFYDDPRSNDGNSYRLQSWLYSSRLLQYSDALEHL
LTTGQGVVLERSIFSDFVFLEAMYNQGFIRKQCVDHYNEVKSVTICDYLPPHLVIYIDVPVPEVQRRIQKKGDPH
EMKITSAYLQDIENAYKKTFLPEMSEKCEVLQYSAREAQDSKKVVEDIEYLKFDKGPWLKQDNRTLYHLRLLVQD
KFEVLNYTSIPIFLPEVTIGAHQTDRVLHQFRELPGRKYSPGYNTEVGDKWIWLK
Structural information
Interpro:  IPR031314  IPR015828  IPR027417  
CDD:   cd02030

PDB:  
5XTC 5XTD 5XTH 5XTI
PDBsum:   5XTC 5XTD 5XTH 5XTI
MINT:  
STRING:   ENSP00000252711
Other Databases GeneCards:  NDUFA10  Malacards:  NDUFA10

Gene ontology

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GO accessionTerm nameEvidence codeGo category
GO:0006120 mitochondrial electron tr
ansport, NADH to ubiquino
ne
IBA biological process
GO:0005747 mitochondrial respiratory
chain complex I
IBA cellular component
GO:0005739 mitochondrion
IBA cellular component
GO:0005737 cytoplasm
IBA cellular component
GO:0005747 mitochondrial respiratory
chain complex I
IDA cellular component
GO:0005747 mitochondrial respiratory
chain complex I
IDA cellular component
GO:0032981 mitochondrial respiratory
chain complex I assembly
IMP biological process
GO:0006120 mitochondrial electron tr
ansport, NADH to ubiquino
ne
IEA biological process
GO:0005747 mitochondrial respiratory
chain complex I
IEA cellular component
GO:0055114 oxidation-reduction proce
ss
IEA biological process
GO:0005739 mitochondrion
IEA cellular component
GO:0070469 respirasome
IEA cellular component
GO:0005743 mitochondrial inner membr
ane
TAS cellular component
GO:0005743 mitochondrial inner membr
ane
TAS cellular component
GO:0005743 mitochondrial inner membr
ane
TAS cellular component
GO:0005743 mitochondrial inner membr
ane
TAS cellular component
GO:0005743 mitochondrial inner membr
ane
TAS cellular component
GO:0005743 mitochondrial inner membr
ane
TAS cellular component
GO:0005743 mitochondrial inner membr
ane
TAS cellular component
GO:0032981 mitochondrial respiratory
chain complex I assembly
TAS biological process
GO:0006120 mitochondrial electron tr
ansport, NADH to ubiquino
ne
TAS biological process
GO:0006120 mitochondrial electron tr
ansport, NADH to ubiquino
ne
IEA biological process
GO:0008137 NADH dehydrogenase (ubiqu
inone) activity
IEA molecular function
GO:0005759 mitochondrial matrix
IEA cellular component
GO:0005739 mitochondrion
IDA cellular component
GO:0006120 mitochondrial electron tr
ansport, NADH to ubiquino
ne
NAS biological process
GO:0005747 mitochondrial respiratory
chain complex I
NAS cellular component
GO:0008137 NADH dehydrogenase (ubiqu
inone) activity
NAS molecular function

KEGG pathways

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Pathway idPathway name
hsa01100Metabolic pathways
hsa05010Alzheimer disease
hsa05016Huntington disease
hsa05012Parkinson disease
hsa04714Thermogenesis
hsa04723Retrograde endocannabinoid signaling
hsa00190Oxidative phosphorylation
hsa04932Non-alcoholic fatty liver disease
Associated diseases References
Leigh syndrome KEGG:H01354
Leigh syndrome KEGG:H01354
Aberrant CpGs in Low Motility Sperm MIK: 21674046
Cryptorchidism MIK: 28606200

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
Show abstract
28606200 Cryptorchi
dism

Monozgotic twin
s (1 control, I
cwith cryptorc
hidism)
Male infertility MeDIP-Seq
Show abstract