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Details
Link-It Detail - Jax Mouse Phenotype - abnormal mitochondrial physiology
Debug Stats
  • ### Total Build Time: 154 ms 22.405 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 237 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
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 579 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.970 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.564 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=147 ms Completed: 147 ms rowSize= 16.374 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal mitochondrial physiology MP:0006036
Definition (1)
any functional anomaly of the cellular organelles responsible for energy production
Parents (1)
img abnormal cell physiology MP:0005621
Children (4)
img abnormal respiratory electron transport chain MP:0010955
img abnormal tricarboxylic acid cycle MP:0010958
img abnormal oxidative phosphorylation MP:0010959
img abnormal mitochondrial proliferation MP:0006037
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053844img abnormal cell physiology MP:0005621
Genes (105)

Species:
human : 105
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanTHEM5284486thioesterase superfamily member 5
INFERRED
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanRNASEH1246243ribonuclease H1
INFERRED
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
Click here to display 86 evidence detail records.
HumanMTERFD2130916MTERF domain containing 2
Click here to display 86 evidence detail records.
HumanTOP1MT116447topoisomerase (DNA) I, mitochondrial
Click here to display 86 evidence detail records.
HumanEGLN2112398egl-9 family hypoxia-inducible factor 2
Click here to display 86 evidence detail records.
HumanPNPT187178polyribonucleotide nucleotidyltransferase 1
Click here to display 86 evidence detail records.
HumanNOA184273nitric oxide associated 1
Click here to display 86 evidence detail records.
HumanIMMP2L83943IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae)
INFERRED
HumanMTERFD380298MTERF domain containing 3
INFERRED
HumanPTCD279810pentatricopeptide repeat domain 2
INFERRED
HumanSLC25A2379085solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23
Click here to display 86 evidence detail records.
HumanPINK165018PTEN induced putative kinase 1
Click here to display 86 evidence detail records.
HumanSLC25A1960386solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
Click here to display 86 evidence detail records.
HumanTMEM2757393transmembrane protein 27
INFERRED
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
INFERRED
HumanC12orf557103chromosome 12 open reading frame 5
Click here to display 86 evidence detail records.
HumanCOQ957017coenzyme Q9 homolog (S. cerevisiae)
Click here to display 86 evidence detail records.
HumanC10orf256652chromosome 10 open reading frame 2
INFERRED
HumanCISD155847CDGSH iron sulfur domain 1
INFERRED
HumanMFN155669mitofusin 1
Click here to display 86 evidence detail records.
HumanPARL55486presenilin associated, rhomboid-like
Click here to display 86 evidence detail records.
HumanCHDH55349choline dehydrogenase
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006036abnormal mitochondrial physiology0self