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Details
Link-It Detail - Jax Mouse Phenotype - abnormal synaptic transmission
Debug Stats
  • ### Total Build Time: 60 ms 22.400 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 224 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 184 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= 589 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.865 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.580 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=55 ms Completed: 55 ms rowSize= 15.290 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal synaptic transmission MP:0003635
Definition (1)
defect in the communication from a neuron to a target across a synapse
Synonyms (1)
"abnormal neurotransmission" EXACT
Parents (1)
img abnormal nervous system physiology MP:0003633
Children (6)
img abnormal CNS synaptic transmission MP:0002206
img abnormal channel response MP:0003484
img abnormal neurotransmitter level MP:0002204
img abnormal PNS synaptic transmission MP:0002913
img abnormal paired-pulse facilitation MP:0002918
img abnormal paired-pulse inhibition MP:0004807
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036314img abnormal nervous system physiology MP:0003633
Genes (483)

Species:
human : 483
Page Size
Current 25
  Page 1 of 20
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanUNC13C440279unc-13 homolog C (C. elegans)
INFERRED
HumanEIF2AK4440275eukaryotic translation initiation factor 2 alpha kinase 4
INFERRED
HumanGRID2IP392862glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein
INFERRED
HumanAGRN375790agrin
INFERRED
HumanNPAS4266743neuronal PAS domain protein 4
INFERRED
HumanNALCN259232sodium leak channel, non-selective
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanSPRED1161742sprouty-related, EVH1 domain containing 1
INFERRED
HumanGRASP160622GRP1 (general receptor for phosphoinositides 1)-associated scaffold protein
INFERRED
HumanSLC32A1140679solute carrier family 32 (GABA vesicular transporter), member 1
INFERRED
HumanSTXBP5134957syntaxin binding protein 5 (tomosyn)
INFERRED
HumanTAAR1134864trace amine associated receptor 1
INFERRED
HumanSYT2127833synaptotagmin II
INFERRED
HumanRAVER1125950ribonucleoprotein, PTB-binding 1
INFERRED
HumanSEZ6124925seizure related 6 homolog (mouse)
INFERRED
HumanRLN3117579relaxin 3
INFERRED
HumanGRIN3A116443glutamate receptor, ionotropic, N-methyl-D-aspartate 3A
INFERRED
HumanLYPD1116372LY6/PLAUR domain containing 1
INFERRED
HumanRAB3C115827RAB3C, member RAS oncogene family
INFERRED
HumanBTBD9114781BTB (POZ) domain containing 9
Click here to display 37 evidence detail records.
HumanSTX1B112755syntaxin 1B
INFERRED
HumanFOXP293986forkhead box P2
INFERRED
HumanCADPS293664Ca++-dependent secretion activator 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003635abnormal synaptic transmission0self