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Details
Link-It Detail - Jax Mouse Phenotype - abnormal oxidative phosphorylation
Debug Stats
  • ### Total Build Time: 25 ms 22.489 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 421 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 620 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.573 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 17.622 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal oxidative phosphorylation MP:0010959
Definition (1)
any anomaly in the process of phosphorylation of ADP to ATP that accompanies the oxidation of a metabolite through the operation of the respiratory chain; oxidation of compounds establishes a proton gradient across the membrane, providing the energy for ATP synthesis
Parents (1)
img abnormal mitochondrial physiology MP:0006036
Children (1)
img abnormal mitochondrial ATP synthesis coupled electron transport MP:0010956
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053845img abnormal mitochondrial physiology MP:0006036
Genes (29)

Species:
human : 29
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanPNPT187178polyribonucleotide nucleotidyltransferase 1
INFERRED
HumanNOA184273nitric oxide associated 1
INFERRED
HumanMTERFD380298MTERF domain containing 3
INFERRED
HumanPTCD279810pentatricopeptide repeat domain 2
INFERRED
HumanPINK165018PTEN induced putative kinase 1
INFERRED
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
INFERRED
HumanCOQ957017coenzyme Q9 homolog (S. cerevisiae)
INFERRED
HumanCISD155847CDGSH iron sulfur domain 1
INFERRED
HumanMTERFD151001MTERF domain containing 1
INFERRED
HumanCOX1710063COX17 cytochrome c oxidase copper chaperone
INFERRED
HumanDNM1L10059dynamin 1-like
INFERRED
HumanSCO29997SCO2 cytochrome c oxidase assembly protein
INFERRED
HumanMTFR19650mitochondrial fission regulator 1
INFERRED
HumanAIFM19131apoptosis-inducing factor, mitochondrion-associated, 1
INFERRED
HumanSQSTM18878sequestosome 1
INFERRED
HumanUPP17378uridine phosphorylase 1
INFERRED
HumanUCP37352uncoupling protein 3 (mitochondrial, proton carrier)
INFERRED
HumanTK27084thymidine kinase 2, mitochondrial
INFERRED
HumanTHRA7067thyroid hormone receptor, alpha
INFERRED
HumanTFAM7019transcription factor A, mitochondrial
INFERRED
HumanPEX55830peroxisomal biogenesis factor 5
INFERRED
HumanPOLG5428polymerase (DNA directed), gamma
img Jax MP, Pubmed Id: 12145814, MOUSE PHENOTYPE ID: MGI:1203517
img Jax MP, Pubmed Id: 12101247, MOUSE PHENOTYPE ID: MGI:88579
img Jax MP, Pubmed Id: 23418460, MOUSE PHENOTYPE ID: MGI:1196389
img Jax MP, Pubmed Id: 23418460, MOUSE PHENOTYPE ID: MGI:3776661
img Jax MP, Pubmed Id: 23418460, MOUSE PHENOTYPE ID: MGI:1196389
HumanPARK25071parkinson protein 2, E3 ubiquitin protein ligase (parkin)
INFERRED
HumanNDUFS44724NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010959abnormal oxidative phosphorylation0self