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Details
Link-It Detail - Jax Mouse Phenotype - abnormal synapse morphology
Debug Stats
  • ### Total Build Time: 159 ms 20.649 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 396 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=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=10 ms Completed: 10 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 1.046 KB
  • 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=127 ms Completed: 127 ms rowSize= 15.395 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal synapse morphology MP:0009538
Definition (1)
any structural anomaly of the membrane junction site of a nerve cell to a target cell, such as another nerve cell, an effector cell, or a sensory receptor cell; transmission of nerve impulses may be mediated by chemical or by electrical means
Parents (1)
img abnormal neuron morphology MP:0002882
Children (2)
img abnormal synaptic vesicle morphology MP:0004769
img abnormal neuromuscular synapse morphology MP:0001053
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal neuron morphology MP:0002882
Genes (115)

Species:
human : 115
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanAGRN375790agrin
INFERRED
HumanLRRTM1347730leucine rich repeat transmembrane neuronal 1
Click here to display 37 evidence detail records.
HumanKY339855kyphoscoliosis peptidase
INFERRED
HumanDOK7285489docking protein 7
INFERRED
HumanFBXO45200933F-box protein 45
INFERRED
HumanLRSAM190678leucine rich repeat and sterile alpha motif containing 1
INFERRED
HumanSTON285439stonin 2
INFERRED
HumanNKX6-284504
INFERRED
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
INFERRED
HumanISL264843ISL LIM homeobox 2
INFERRED
HumanNEUROD663974neuronal differentiation 6
Click here to display 37 evidence detail records.
HumanNAPB63908N-ethylmaleimide-sensitive factor attachment protein, beta
INFERRED
HumanSLC5A760482solute carrier family 5 (sodium/choline cotransporter), member 7
INFERRED
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
INFERRED
HumanSCYL157410SCY1-like 1 (S. cerevisiae)
INFERRED
HumanSLC17A657084solute carrier family 17 (vesicular glutamate transporter), member 6
INFERRED
HumanSLC17A757030solute carrier family 17 (vesicular glutamate transporter), member 7
INFERRED
HumanDACT151339dishevelled-binding antagonist of beta-catenin 1
Click here to display 37 evidence detail records.
HumanNRN151299neuritin 1
Click here to display 37 evidence detail records.
HumanPCLO27445piccolo presynaptic cytomatrix protein
INFERRED
HumanFGF2227006fibroblast growth factor 22
INFERRED
HumanNBEA26960neurobeachin
Click here to display 37 evidence detail records.
HumanERC226059ELKS/RAB6-interacting/CAST family member 2
Click here to display 37 evidence detail records.
HumanCLIP325999CAP-GLY domain containing linker protein 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009538abnormal synapse morphology0self