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Details
Link-It Detail - Jax Mouse Phenotype - abnormal nerve conduction
Debug Stats
  • ### Total Build Time: 82 ms 20.855 KB
  • CONCEPT_NAME gt=13 ms Completed: 13 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 221 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=4 ms Completed: 4 ms rowSize= 596 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.039 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=58 ms Completed: 58 ms rowSize= 15.755 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal nerve conduction MP:0005403
Definition (1)
anomaly in the act of transmitting electricity along a single nerve
Parents (1)
img abnormal nervous system electrophysiology MP:0002272
Children (2)
img decreased nerve conduction velocity MP:0008814
img increased nerve conduction velocity MP:0011994
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal nervous system electrophysiology MP:0002272
Genes (52)

Species:
human : 52
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanNALCN259232sodium leak channel, non-selective
Click here to display 52 evidence detail records.
HumanFGD4121512FYVE, RhoGEF and PH domain containing 4
INFERRED
HumanLRSAM190678leucine rich repeat and sterile alpha motif containing 1
INFERRED
HumanPARP1084875poly (ADP-ribose) polymerase family, member 10
INFERRED
HumanNKX6-284504
Click here to display 52 evidence detail records.
HumanSBF281846SET binding factor 2
Click here to display 52 evidence detail records.
HumanSH3TC279628SH3 domain and tetratricopeptide repeats 2
INFERRED
HumanEBF264641early B-cell factor 2
INFERRED
HumanPRX57716periaxin
Click here to display 52 evidence detail records.
HumanERBB2IP55914erbb2 interacting protein
INFERRED
HumanPARL55486presenilin associated, rhomboid-like
Click here to display 52 evidence detail records.
HumanLPIN123175lipin 1
INFERRED
HumanNFASC23114neurofascin
INFERRED
HumanSIRT222933sirtuin 2
INFERRED
HumanNDRG110397N-myc downstream regulated 1
INFERRED
HumanFIG49896FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
INFERRED
HumanMTMR28898myotubularin related protein 2
Click here to display 52 evidence detail records.
HumanCNTNAP18506contactin associated protein 1
Click here to display 52 evidence detail records.
HumanGNPAT8443glyceronephosphate O-acyltransferase
INFERRED
HumanUGT87368UDP glycosyltransferase 8
Click here to display 52 evidence detail records.
HumanTNR7143tenascin R
INFERRED
HumanSLC5A36526solute carrier family 5 (sodium/myo-inositol cotransporter), member 3
Click here to display 52 evidence detail records.
HumanSLC1A66511solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6
Click here to display 52 evidence detail records.
HumanSLC1A16505solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
Click here to display 52 evidence detail records.
HumanSHC16464SHC (Src homology 2 domain containing) transforming protein 1
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005403abnormal nerve conduction0self