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Details
Link-It Detail - Jax Mouse Phenotype - abnormal PML bodies
Debug Stats
  • ### Total Build Time: 80 ms 5.984 KB
  • CONCEPT_NAME gt=3 ms Completed: 2 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 361 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 180 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=52 ms Completed: 52 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.572 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 1.644 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal PML bodies MP:0008886
Definition (1)
alteration in structure, number or location of the subnuclear structures associated with functions including transcription, DNA repair, viral defense, stress, cell cycle regulation, proteolysis and apoptosis
Synonyms (1)
"abnormal SP-100 bodies" EXACT
Parents (1)
img abnormal cell nucleus morphology MP:0003111
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053845img abnormal cell nucleus morphology MP:0003111
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanSUMO17341small ubiquitin-like modifier 1
img Jax MP, Pubmed Id: 19033381, MOUSE PHENOTYPE ID: MGI:1197010
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008886abnormal PML bodies0self