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Details
Link-It Detail - Jax Mouse Phenotype - abnormal touch/ nociception
Debug Stats
  • ### Total Build Time: 154 ms 24.856 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 313 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=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=12 ms Completed: 12 ms rowSize= 1.037 KB
  • CONCEPT_CHILDREN gt=14 ms Completed: 14 ms rowSize= 3.298 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.931 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=103 ms Completed: 103 ms rowSize= 15.423 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=5 ms Completed: 5 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal touch/ nociception MP:0001968
Definition (1)
change in the ability to sense contact with objects or in the ability to sense pain, most often registered by mechanoreceptors in the skin and mucous membranes
Synonyms (1)
"touch/ nociception defects" EXACT
Parents (2)
img abnormal sensory capabilities/reflexes/nociception MP:0002067
img integument phenotype MP:0010771
Children (7)
img abnormal response to tactile stimuli MP:0005316
img abnormal chemical nociception MP:0002735
img abnormal thermal nociception MP:0002733
img abnormal nociception after inflammation MP:0002736
img abnormal pain threshold MP:0001970
img analgesia MP:0004270
img abnormal mechanical nociception MP:0002734
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053865img abnormal sensory capabilities/reflexes/nociception MP:0002067
img mammalian phenotype MP:0000001img integument phenotype MP:00107713img integument phenotype MP:0010771
Genes (206)

Species:
human : 206
Page Size
Current 25
  Page 1 of 9
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMINOS1-NBL1100532736
INFERRED
HumanPIRT644139phosphoinositide-interacting regulator of transient receptor potential channels
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
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
INFERRED
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
INFERRED
HumanPRX57716periaxin
Click here to display 26 evidence detail records.
HumanTSHZ357616teashirt zinc finger homeobox 3
INFERRED
HumanSLC12A557468solute carrier family 12 (potassium/chloride transporter), member 5
Click here to display 26 evidence detail records.
HumanLPAR557121lysophosphatidic acid receptor 5
INFERRED
HumanSLC17A657084solute carrier family 17 (vesicular glutamate transporter), member 6
INFERRED
HumanSLC17A757030solute carrier family 17 (vesicular glutamate transporter), member 7
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001968abnormal touch/ nociception0self