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Details
Link-It Detail - Jax Mouse Phenotype - hippocampal neuron degeneration
Debug Stats
  • ### Total Build Time: 97 ms 19.281 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 248 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 190 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 1.024 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=20 ms Completed: 20 ms rowSize= 5.616 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=64 ms Completed: 64 ms rowSize= 10.511 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
hippocampal neuron degeneration MP:0000811
Definition (1)
a retrogressive impairment of function or destruction of the neuronal cells in the hippocampus
Synonyms (1)
"degenerating hippocampal neurons" EXACT
Parents (2)
img neuron degeneration MP:0003224
img abnormal hippocampus neuron morphology MP:0009939
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img neuron degeneration MP:0003224
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal hippocampus neuron morphology MP:0009939
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal hippocampus neuron morphology MP:0009939
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal hippocampus neuron morphology MP:0009939
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
Click here to display 42 evidence detail records.
HumanSTAMBP10617STAM binding protein
Click here to display 42 evidence detail records.
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
Click here to display 42 evidence detail records.
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Click here to display 42 evidence detail records.
HumanUQCRFS17386ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1
Click here to display 42 evidence detail records.
HumanPTEN5728phosphatase and tensin homolog
Click here to display 42 evidence detail records.
HumanPPT15538palmitoyl-protein thioesterase 1
Click here to display 42 evidence detail records.
HumanABCB15243ATP-binding cassette, sub-family B (MDR/TAP), member 1
Click here to display 42 evidence detail records.
HumanPARK25071parkinson protein 2, E3 ubiquitin protein ligase (parkin)
Click here to display 42 evidence detail records.
HumanINPP4A3631inositol polyphosphate-4-phosphatase, type I, 107kDa
Click here to display 42 evidence detail records.
HumanHPCA3208hippocalcin
Click here to display 42 evidence detail records.
HumanGRIA22891glutamate receptor, ionotropic, AMPA 2
Click here to display 42 evidence detail records.
HumanFSHR2492follicle stimulating hormone receptor
Click here to display 42 evidence detail records.
HumanCOX101352cytochrome c oxidase assembly homolog 10 (yeast)
Click here to display 42 evidence detail records.
HumanCLCN71186chloride channel, voltage-sensitive 7
Click here to display 42 evidence detail records.
HumanCLCN31182chloride channel, voltage-sensitive 3
Click here to display 42 evidence detail records.
HumanCAV1857caveolin 1, caveolae protein, 22kDa
Click here to display 42 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000811hippocampal neuron degeneration0self