ENSG00000186010


Homo sapiens

Features
Gene ID: ENSG00000186010
  
Biological name :NDUFA13
  
Synonyms : NADH:ubiquinone oxidoreductase subunit A13 / NDUFA13 / Q9P0J0
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 19
Strand: 1
Band: p13.11
Gene start: 19515736
Gene end: 19529054
  
Corresponding Affymetrix probe sets: 220864_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000467274
Ensembl peptide - ENSP00000476093
Ensembl peptide - ENSP00000468317
Ensembl peptide - ENSP00000423673
Ensembl peptide - ENSP00000465129
NCBI entrez gene - 51079     See in Manteia.
OMIM - 609435
RefSeq - NM_015965
RefSeq Peptide - NP_057049
swissprot - Q9P0J0
swissprot - B4DEZ3
swissprot - U3KQP3
swissprot - K7EJE1
swissprot - K7EP87
Ensembl - ENSG00000186010
  
Related genetic diseases (OMIM): 607464 - {Thyroid carcinoma, Hurthle cell}, 607464
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 ENSGALG00000039212Gallus gallus
 Q9ERS2ENSMUSG00000036199Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
AC011448.1ENSG0000025867478


Protein motifs (from Interpro)
Interpro ID Name
 IPR009346  GRIM-19


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006120 mitochondrial electron transport, NADH to ubiquinone TAS
 biological_processGO:0006915 apoptotic process IEA
 biological_processGO:0010952 positive regulation of peptidase activity IC
 biological_processGO:0030308 negative regulation of cell growth IMP
 biological_processGO:0032981 mitochondrial respiratory chain complex I assembly TAS
 biological_processGO:0035458 cellular response to interferon-beta IDA
 biological_processGO:0043280 positive regulation of cysteine-type endopeptidase activity involved in apoptotic process IGI
 biological_processGO:0045039 protein import into mitochondrial inner membrane IDA
 biological_processGO:0045732 positive regulation of protein catabolic process IGI
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IDA
 biological_processGO:0055114 oxidation-reduction process IEA
 biological_processGO:0071300 cellular response to retinoic acid IDA
 biological_processGO:0072593 reactive oxygen species metabolic process IMP
 biological_processGO:0097190 apoptotic signaling pathway IDA
 biological_processGO:0097191 extrinsic apoptotic signaling pathway IEA
 biological_processGO:2001243 negative regulation of intrinsic apoptotic signaling pathway IMP
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IDA
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005739 mitochondrion IEA
 cellular_componentGO:0005743 mitochondrial inner membrane TAS
 cellular_componentGO:0005746 mitochondrial respiratory chain IDA
 cellular_componentGO:0005747 mitochondrial respiratory chain complex I IMP
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0031966 mitochondrial membrane IDA
 cellular_componentGO:0070062 extracellular exosome HDA
 cellular_componentGO:0070469 respiratory chain IEA
 molecular_functionGO:0003954 NADH dehydrogenase activity IMP
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005524 ATP binding NAS
 molecular_functionGO:0008137 NADH dehydrogenase (ubiquinone) activity IDA


Pathways (from Reactome)
Pathway description
Respiratory electron transport
Complex I biogenesis


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000365 Hearing loss 
Show

 HP:0000486 Strabismus "Strabismus (also known as squint) is a condition in which the eyes are not properly aligned with each other." [HPO:curators]
Show

 HP:0000508 Ptosis "Drooping of the eyelid." [HPO:curators]
Show

 HP:0000580 Pigmentary retinopathy 
Show

 HP:0000602 Ophthalmoplegia 
Show

 HP:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
Show

 HP:0000648 Optic atrophy 
Show

 HP:0000712 Emotional lability 
Show

 HP:0000998 Hypertrichosis "Hypertrichosis is increased hair growth that is abnormal in quantity or location." [HPO:curators]
Show

 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
Show

 HP:0001252 Muscular hypotonia "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators]
Show

 HP:0001260 Dysarthria "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators]
Show

 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
Show

 HP:0001332 Dystonia "An abnormally increased muscular tone that causes fixed abnormal postures. There is a slow, intermittent twisting motion that leads to exaggerated turning and posture of the extremities and trunk." [HPO:curators]
Show

 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
Show

 HP:0001508 Failure to thrive 
Show

 HP:0001629 Ventricular septal defect "A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum." [HPO:curators]
Show

 HP:0001639 Hypertrophic cardiomyopathy 
Show

 HP:0001903 Anemia 
Show

 HP:0002073 Progressive cerebellar ataxia 
Show

 HP:0002104 Apnea "Lack of breathing with no movement of the respiratory muscles and no exchange of air in the lungs. This term refers to a disposition to have recurrent episodes of apnea rather than to a single event." [HPO:curators]
Show

 HP:0002151 Increased serum lactate "Abnormally increased level of blood lactate (2-hydroxypropanoic acid). Lactate is produced from pyruvate by lactate dehydrogenase during normal metabolism." [HPO:curators]
Show

 HP:0002415 Leukodystrophy 
Show

 HP:0002490 Increased CSF lactate "Increased concentration of lactate in the cerebrospinal fluid." [HPO:curators]
Show

 HP:0002928 Decreased activity of the pyruvate dehydrogenase (PDH) complex 
Show

 HP:0007020 Progressive spastic paraplegia 
Show

 HP:0007183 Hyperintense lesions in the basal ganglia on mri 
Show

 HP:0008972 Decreased activities of mitochondrial-encoded respiratory chain complexes 
Show

 HP:0009830 Peripheral neuropathy "Peripheral neuropathy is a general term for any disorder of the peripheral nervous system. The main clinical features used to classify peripheral neuropathy are distribution, type (mainly demyelinating versus mainly axonal), duration, and course." [HPO:curators]
Show

 HP:0010864 Mental retardation, severe "Moderate mental retardation is defined as an intelligence quotient (IQ) in the range of 20-34." [HPO:probinson]
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr