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Details
Link-It Detail - Jax Mouse Phenotype - abnormal startle reflex
Debug Stats
  • ### Total Build Time: 129 ms 22.281 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 279 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=7 ms Completed: 7 ms rowSize= 570 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 1.905 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=7 ms Completed: 7 ms rowSize= 2.902 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=94 ms Completed: 94 ms rowSize= 14.974 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 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 startle reflex MP:0001486
Definition (1)
aberrant threshold or reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch
Parents (1)
img abnormal reflex MP:0001961
Children (4)
img decreased startle reflex MP:0001489
img increased startle reflex MP:0001488
img hyperekplexia MP:0005604
img absent startle reflex MP:0006359
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal reflex MP:0001961
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053867img abnormal reflex MP:0001961
Genes (117)

Species:
human : 117
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanOTOG340990otogelin
INFERRED
HumanTMIE259236transmembrane inner ear
Click here to display 46 evidence detail records.
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
INFERRED
HumanAEBP2121536AE binding protein 2
INFERRED
HumanRLN3117579relaxin 3
INFERRED
HumanFOXP293986forkhead box P2
INFERRED
HumanNAV289797neuron navigator 2
INFERRED
HumanNTNG284628netrin G2
INFERRED
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
INFERRED
HumanPREX280243phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2
INFERRED
HumanFBXO1180204F-box protein 11
INFERRED
HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
INFERRED
HumanLRRC464101leucine rich repeat containing 4
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 46 evidence detail records.
HumanNPAS364067neuronal PAS domain protein 3
Click here to display 46 evidence detail records.
HumanSRR63826serine racemase
INFERRED
HumanSLC17A757030solute carrier family 17 (vesicular glutamate transporter), member 7
INFERRED
HumanBARHL156751BarH-like homeobox 1
INFERRED
HumanELMOD155531ELMO/CED-12 domain containing 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001486abnormal startle reflex0self