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Details
Link-It Detail - Jax Mouse Phenotype - impaired ability to fire action potentials
Debug Stats
  • ### Total Build Time: 61 ms 12.949 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 412 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 281 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=6 ms Completed: 6 ms rowSize= 580 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.571 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 8.803 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.180 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
impaired ability to fire action potentials MP:0002578
Definition (1)
anomaly resulting in reduced changes in membrane potentials occurring in nerve or other excitable tissue when excitation occurs
Parents (1)
img abnormal action potential MP:0005402
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal action potential MP:0005402
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanNEUROD663974neuronal differentiation 6
Click here to display 19 evidence detail records.
HumanSLC12A557468solute carrier family 12 (potassium/chloride transporter), member 5
Click here to display 19 evidence detail records.
HumanNFASC23114neurofascin
Click here to display 19 evidence detail records.
HumanCACNA1G8913calcium channel, voltage-dependent, T type, alpha 1G subunit
Click here to display 19 evidence detail records.
HumanMADD8567MAP-kinase activating death domain
Click here to display 19 evidence detail records.
HumanTRPV17442transient receptor potential cation channel, subfamily V, member 1
Click here to display 19 evidence detail records.
HumanSCN10A6336sodium channel, voltage-gated, type X, alpha subunit
Click here to display 19 evidence detail records.
HumanSCN1A6323sodium channel, voltage-gated, type I, alpha subunit
Click here to display 19 evidence detail records.
HumanOPRM14988opioid receptor, mu 1
Click here to display 19 evidence detail records.
HumanKCNMA13778potassium large conductance calcium-activated channel, subfamily M, alpha member 1
Click here to display 19 evidence detail records.
HumanKCNA23737potassium voltage-gated channel, shaker-related subfamily, member 2
Click here to display 19 evidence detail records.
HumanGRIA42893glutamate receptor, ionotropic, AMPA 4
Click here to display 19 evidence detail records.
HumanETV12115ets variant 1
Click here to display 19 evidence detail records.
HumanANK3288ankyrin 3, node of Ranvier (ankyrin G)
Click here to display 19 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002578impaired ability to fire action potentials0self