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Details
Link-It Detail - Jax Mouse Phenotype - abnormal action potential
Debug Stats
  • ### Total Build Time: 481 ms 21.631 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 241 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=2 ms Completed: 2 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= 596 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 1.060 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.587 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=467 ms Completed: 467 ms rowSize= 16.490 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal action potential MP:0005402
Definition (1)
change in the electric response of a nerve or other excitable tissue to its stimulation
Parents (1)
img abnormal nervous system electrophysiology MP:0002272
Children (2)
img abnormal cochlear nerve compound action potential MP:0004415
img impaired ability to fire action potentials MP:0002578
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal nervous system electrophysiology MP:0002272
Genes (92)

Species:
human : 92
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
Click here to display 92 evidence detail records.
HumanKCNK18338567potassium channel, subfamily K, member 18
Click here to display 92 evidence detail records.
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanOTOS150677otospiralin
INFERRED
HumanOTOA146183otoancorin
INFERRED
HumanFGD4121512FYVE, RhoGEF and PH domain containing 4
Click here to display 92 evidence detail records.
HumanLRRK2120892leucine-rich repeat kinase 2
Click here to display 92 evidence detail records.
HumanESPN83715espin
INFERRED
HumanSBF281846SET binding factor 2
Click here to display 92 evidence detail records.
HumanCDH2364072cadherin-related 23
INFERRED
HumanNEUROD663974neuronal differentiation 6
INFERRED
HumanPRX57716periaxin
Click here to display 92 evidence detail records.
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
Click here to display 92 evidence detail records.
HumanHCN357657hyperpolarization activated cyclic nucleotide-gated potassium channel 3
Click here to display 92 evidence detail records.
HumanSLC12A557468solute carrier family 12 (potassium/chloride transporter), member 5
Click here to display 92 evidence detail records.
HumanGJD257369gap junction protein, delta 2, 36kDa
Click here to display 92 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanKCNK951305potassium channel, subfamily K, member 9
Click here to display 92 evidence detail records.
HumanDYNC1LI151143dynein, cytoplasmic 1, light intermediate chain 1
Click here to display 92 evidence detail records.
HumanHTRA227429HtrA serine peptidase 2
Click here to display 92 evidence detail records.
HumanKCNMB427345potassium large conductance calcium-activated channel, subfamily M, beta member 4
Click here to display 92 evidence detail records.
HumanLPIN123175lipin 1
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HumanNFASC23114neurofascin
Click here to display 92 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005402abnormal action potential0self