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Details
Link-It Detail - Jax Mouse Phenotype - abnormal sensory capabilities/reflexes/nociception
Debug Stats
  • ### Total Build Time: 187 ms 21.947 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 428 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 215 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 238 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= 572 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 2.361 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=151 ms Completed: 151 ms rowSize= 15.265 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.188 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal sensory capabilities/reflexes/nociception MP:0002067
Definition (1)
inability or altered ability to respond to a sensory stimulus
Synonyms (1)
"neurological/behavioral: sensory capabilities/reflexes/nociception abnormalities" EXACT
Parents (1)
img abnormal behavior MP:0004924
Children (5)
img hyperresponsive MP:0001400
img abnormal touch escape response MP:0012001
img abnormal reflex MP:0001961
img abnormal thermosensation MP:0003663
img abnormal touch/ nociception MP:0001968
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053864img abnormal behavior MP:0004924
Genes (564)

Species:
human : 564
Page Size
Current 25
  Page 1 of 23
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMINOS1-NBL1100532736
INFERRED
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanPIRT644139phosphoinositide-interacting regulator of transient receptor potential channels
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanSPRN503542shadow of prion protein homolog (zebrafish)
INFERRED
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED
HumanCCL3L3414062chemokine (C-C motif) ligand 3-like 3
INFERRED
HumanGRID2IP392862glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein
INFERRED
HumanHELT391723helt bHLH transcription factor
INFERRED
HumanFEZF1389549FEZ family zinc finger 1
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanACSM4341392acyl-CoA synthetase medium-chain family member 4
Click here to display 29 evidence detail records.
HumanOTOG340990otogelin
INFERRED
HumanSUMF1285362sulfatase modifying factor 1
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanNPB256933neuropeptide B
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanGSX1219409GS homeobox 1
INFERRED
HumanARX170302aristaless related homeobox
INFERRED
HumanLGI4163175leucine-rich repeat LGI family, member 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002067abnormal sensory capabilities/reflexes/nociception0self