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Details
Link-It Detail - Jax Mouse Phenotype - decreased CNS synapse formation
Debug Stats
  • ### Total Build Time: 73 ms 13.983 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 281 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 187 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=6 ms Completed: 6 ms rowSize= 585 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=7 ms Completed: 7 ms rowSize= 1.576 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 9.677 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
decreased CNS synapse formation MP:0004998
Definition (1)
a reduction in the frequency of the process of generating the initial connections between an axon and effector tissue or neuron
Synonyms (1)
"reduced CNS synapse formation" EXACT
Parents (1)
img abnormal CNS synapse formation MP:0004996
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal CNS synapse formation MP:0004996
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanAGRN375790agrin
Click here to display 17 evidence detail records.
HumanCC2D1A54862coiled-coil and C2 domain containing 1A
Click here to display 17 evidence detail records.
HumanACTL6B51412actin-like 6B
Click here to display 17 evidence detail records.
HumanNCSTN23385nicastrin
Click here to display 17 evidence detail records.
HumanKLK811202kallikrein-related peptidase 8
Click here to display 17 evidence detail records.
HumanCACNG210369calcium channel, voltage-dependent, gamma subunit 2
Click here to display 17 evidence detail records.
HumanDNM1L10059dynamin 1-like
Click here to display 17 evidence detail records.
HumanNRXN29379neurexin 2
Click here to display 17 evidence detail records.
HumanKALRN8997kalirin, RhoGEF kinase
Click here to display 17 evidence detail records.
HumanSTAU16780staufen double-stranded RNA binding protein 1
Click here to display 17 evidence detail records.
HumanPURA5813purine-rich element binding protein A
Click here to display 17 evidence detail records.
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
Click here to display 17 evidence detail records.
HumanSMAD24087SMAD family member 2
Click here to display 17 evidence detail records.
HumanFOXG12290forkhead box G1
Click here to display 17 evidence detail records.
HumanCAV1857caveolin 1, caveolae protein, 22kDa
Click here to display 17 evidence detail records.
HumanBCL2L2599BCL2-like 2
Click here to display 17 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004998decreased CNS synapse formation0self