Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Jax Mouse Phenotype - abnormal mitochondrion morphology
Debug Stats
  • ### Total Build Time: 237 ms 24.936 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 384 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 191 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=2 ms Completed: 2 ms rowSize= 579 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 3.800 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.564 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=229 ms Completed: 229 ms rowSize= 16.744 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 mitochondrion morphology MP:0006035
Definition (1)
any structural anomaly of the semiautonomous, self replicating organelles that occur in varying numbers, shapes, and sizes in the cytoplasm of virtually all eukaryotic cells; mitochondria are notably the site of tissue respiration
Synonyms (1)
"abnormal mitochondrial morphology" EXACT
Parents (1)
img abnormal cell morphology MP:0000358
Children (8)
img decreased mitochondria number MP:0011629
img abnormal mitochondrial matrix morphology MP:0011637
img abnormal mitochondrial shape MP:0011633
img abnormal mitochondrial inner membrane morphology MP:0011634
img increased mitochondria size MP:0011630
img increased mitochondria number MP:0011628
img abnormal mitochondrial chromosome morphology MP:0011638
img decreased mitochondria size MP:0011631
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053844img abnormal cell morphology MP:0000358
Genes (91)

Species:
human : 91
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
Click here to display 117 evidence detail records.
HumanTHEM5284486thioesterase superfamily member 5
Click here to display 117 evidence detail records.
HumanRNASEH1246243ribonuclease H1
Click here to display 117 evidence detail records.
HumanPLD6201164phospholipase D family, member 6
Click here to display 117 evidence detail records.
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
Click here to display 117 evidence detail records.
HumanTOP1MT116447topoisomerase (DNA) I, mitochondrial
Click here to display 117 evidence detail records.
HumanOMA1115209OMA1 zinc metallopeptidase
Click here to display 117 evidence detail records.
HumanPTPMT1114971protein tyrosine phosphatase, mitochondrial 1
Click here to display 117 evidence detail records.
HumanPNPT187178polyribonucleotide nucleotidyltransferase 1
INFERRED
HumanNOA184273nitric oxide associated 1
Click here to display 117 evidence detail records.
HumanSESN283667sestrin 2
INFERRED
HumanMTERFD380298MTERF domain containing 3
INFERRED
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Click here to display 117 evidence detail records.
HumanPTCD279810pentatricopeptide repeat domain 2
Click here to display 117 evidence detail records.
HumanPINK165018PTEN induced putative kinase 1
Click here to display 117 evidence detail records.
HumanMKL157591megakaryoblastic leukemia (translocation) 1
Click here to display 117 evidence detail records.
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
Click here to display 117 evidence detail records.
HumanPNPLA257104patatin-like phospholipase domain containing 2
Click here to display 117 evidence detail records.
HumanC12orf557103chromosome 12 open reading frame 5
INFERRED
HumanC10orf256652chromosome 10 open reading frame 2
Click here to display 117 evidence detail records.
HumanMFN155669mitofusin 1
Click here to display 117 evidence detail records.
HumanCHDH55349choline dehydrogenase
INFERRED
HumanEGLN154583egl-9 family hypoxia-inducible factor 1
INFERRED
HumanADIPOR151094adiponectin receptor 1
Click here to display 117 evidence detail records.
HumanNDUFA1351079NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006035abnormal mitochondrion morphology0self