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Details
Link-It Detail - Jax Mouse Phenotype - abnormal pain threshold
Debug Stats
  • ### Total Build Time: 55 ms 23.077 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 212 bytes
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  • 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
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.899 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.915 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 15.816 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.161 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal pain threshold MP:0001970
Definition (1)
increased or decreased average level of perception of pain
Parents (1)
img abnormal touch/ nociception MP:0001968
Children (4)
img abnormal chemically-elicited antinociception MP:0001980
img hypoalgesia MP:0003043
img hyperalgesia MP:0005407
img allodynia MP:0003177
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal touch/ nociception MP:0001968
img mammalian phenotype MP:0000001img integument phenotype MP:00107714img abnormal touch/ nociception MP:0001968
Genes (171)

Species:
human : 171
Page Size
Current 25
  Page 1 of 7
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMINOS1-NBL1100532736
Click here to display 41 evidence detail records.
HumanPIRT644139phosphoinositide-interacting regulator of transient receptor potential channels
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
Click here to display 41 evidence detail records.
HumanNPB256933neuropeptide B
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanARX170302aristaless related homeobox
INFERRED
HumanTRPV3162514transient receptor potential cation channel, subfamily V, member 3
INFERRED
HumanSTOML3161003stomatin (EPB72)-like 3
INFERRED
HumanGRASP160622GRP1 (general receptor for phosphoinositides 1)-associated scaffold protein
INFERRED
HumanTPH2121278tryptophan hydroxylase 2
INFERRED
HumanMRGPRD116512MAS-related GPR, member D
INFERRED
HumanNAV289797neuron navigator 2
INFERRED
HumanPOMK84197protein-O-mannose kinase
INFERRED
HumanPPP1R14C81706protein phosphatase 1, regulatory (inhibitor) subunit 14C
INFERRED
HumanTRPM380036transient receptor potential cation channel, subfamily M, member 3
INFERRED
HumanTRPM879054transient receptor potential cation channel, subfamily M, member 8
Click here to display 41 evidence detail records.
HumanVWA164856von Willebrand factor A domain containing 1
INFERRED
HumanSLC5A760482solute carrier family 5 (sodium/choline cotransporter), member 7
INFERRED
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
Click here to display 41 evidence detail records.
HumanPRX57716periaxin
INFERRED
HumanTSHZ357616teashirt zinc finger homeobox 3
INFERRED
HumanLPAR557121lysophosphatidic acid receptor 5
INFERRED
HumanSLC17A657084solute carrier family 17 (vesicular glutamate transporter), member 6
Click here to display 41 evidence detail records.
HumanLXN56925latexin
INFERRED
HumanNMUR256923neuromedin U receptor 2
Click here to display 41 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001970abnormal pain threshold0self