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Details
Link-It Detail - Jax Mouse Phenotype - axonal dystrophy
Debug Stats
  • ### Total Build Time: 20 ms 10.606 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 360 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 249 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=3 ms Completed: 3 ms rowSize= 572 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.563 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 6.583 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
axonal dystrophy MP:0003225
Definition (1)
axon degeneration that may result from genetic abnormalities or inadequate or faulty metabolism
Parents (1)
img axon degeneration MP:0005405
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img axon degeneration MP:0005405
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanSPTBN457731spectrin, beta, non-erythrocytic 4
Click here to display 31 evidence detail records.
HumanATP8A251761ATPase, aminophospholipid transporter, class I, type 8A, member 2
Click here to display 31 evidence detail records.
HumanUBE4B10277ubiquitination factor E4B
Click here to display 31 evidence detail records.
HumanEI249538etoposide induced 2.4
Click here to display 31 evidence detail records.
HumanCACNA2D29254calcium channel, voltage-dependent, alpha 2/delta subunit 2
Click here to display 31 evidence detail records.
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
Click here to display 31 evidence detail records.
HumanUCHL37347ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase)
Click here to display 31 evidence detail records.
HumanUCHL17345ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
Click here to display 31 evidence detail records.
HumanKLC13831kinesin light chain 1
Click here to display 31 evidence detail records.
HumanDOCK31795dedicator of cytokinesis 3
Click here to display 31 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003225axonal dystrophy0self