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Details
Link-It Detail - Jax Mouse Phenotype - axon degeneration
Debug Stats
  • ### Total Build Time: 537 ms 22.192 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 362 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 223 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 177 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=0 Completed: 0 ms rowSize= 572 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.002 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.563 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=518 ms Completed: 518 ms rowSize= 17.024 KB
  • CONCEPT_XREFS gt=10 ms Completed: 10 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
axon degeneration MP:0005405
Definition (1)
retrogressive pathologic change in the single process of a nerve cell
Synonyms (1)
"axonal degeneration" EXACT
Parents (1)
img neurodegeneration MP:0002229
Children (2)
img axonal dystrophy MP:0003225
img axonal spheroids MP:0010047
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img neurodegeneration MP:0002229
Genes (58)

Species:
human : 58
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SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
Click here to display 114 evidence detail records.
HumanLRSAM190678leucine rich repeat and sterile alpha motif containing 1
Click here to display 114 evidence detail records.
HumanNKX6-284504
Click here to display 114 evidence detail records.
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Click here to display 114 evidence detail records.
HumanLYNX166004Ly6/neurotoxin 1
Click here to display 114 evidence detail records.
HumanSPTBN457731spectrin, beta, non-erythrocytic 4
INFERRED
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
Click here to display 114 evidence detail records.
HumanCLN654982ceroid-lipofuscinosis, neuronal 6, late infantile, variant
Click here to display 114 evidence detail records.
HumanATP8A251761ATPase, aminophospholipid transporter, class I, type 8A, member 2
INFERRED
HumanLPIN123175lipin 1
Click here to display 114 evidence detail records.
HumanNMNAT223057nicotinamide nucleotide adenylyltransferase 2
Click here to display 114 evidence detail records.
HumanCHL110752cell adhesion molecule L1-like
Click here to display 114 evidence detail records.
HumanAVIL10677advillin
Click here to display 114 evidence detail records.
HumanATG710533autophagy related 7
Click here to display 114 evidence detail records.
HumanUBE4B10277ubiquitination factor E4B
INFERRED
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
Click here to display 114 evidence detail records.
HumanEI249538etoposide induced 2.4
Click here to display 114 evidence detail records.
HumanCACNA2D29254calcium channel, voltage-dependent, alpha 2/delta subunit 2
INFERRED
HumanMTMR28898myotubularin related protein 2
Click here to display 114 evidence detail records.
HumanSQSTM18878sequestosome 1
Click here to display 114 evidence detail records.
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
Click here to display 114 evidence detail records.
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Click here to display 114 evidence detail records.
HumanVEGFA7422vascular endothelial growth factor A
Click here to display 114 evidence detail records.
HumanUCHL37347ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase)
INFERRED
HumanUCHL17345ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
Click here to display 114 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005405axon degeneration0self