Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Jax Mouse Phenotype - increased startle reflex
Debug Stats
  • ### Total Build Time: 148 ms 22.795 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 290 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 209 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=2 ms Completed: 2 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.918 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=140 ms Completed: 140 ms rowSize= 17.144 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
increased startle reflex MP:0001488
Definition (1)
reduced threshold or more severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch
Synonyms (1)
"increased startle response in acoustic startle test" EXACT
Parents (1)
img abnormal startle reflex MP:0001486
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053867img abnormal startle reflex MP:0001486
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053868img abnormal startle reflex MP:0001486
Genes (41)

Species:
human : 41
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRLN3117579relaxin 3
Click here to display 106 evidence detail records.
HumanPREX280243phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2
Click here to display 106 evidence detail records.
HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
Click here to display 106 evidence detail records.
HumanSRR63826serine racemase
Click here to display 106 evidence detail records.
HumanSLC17A757030solute carrier family 17 (vesicular glutamate transporter), member 7
Click here to display 106 evidence detail records.
HumanNXPH311248neurexophilin 3
Click here to display 106 evidence detail records.
HumanATE111101arginyltransferase 1
Click here to display 106 evidence detail records.
HumanATF711016activating transcription factor 7
Click here to display 106 evidence detail records.
HumanPPARGC1A10891peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
Click here to display 106 evidence detail records.
HumanCPLX210814complexin 2
Click here to display 106 evidence detail records.
HumanSYNGAP18831synaptic Ras GTPase activating protein 1
Click here to display 106 evidence detail records.
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Click here to display 106 evidence detail records.
HumanZIC27546Zic family member 2
Click here to display 106 evidence detail records.
HumanUCN7349urocortin
Click here to display 106 evidence detail records.
HumanTSC17248tuberous sclerosis 1
Click here to display 106 evidence detail records.
HumanSTX1A6804syntaxin 1A (brain)
Click here to display 106 evidence detail records.
HumanSLC6A16529solute carrier family 6 (neurotransmitter transporter), member 1
Click here to display 106 evidence detail records.
HumanSLC2A36515solute carrier family 2 (facilitated glucose transporter), member 3
Click here to display 106 evidence detail records.
HumanPTGER15731prostaglandin E receptor 1 (subtype EP1), 42kDa
Click here to display 106 evidence detail records.
HumanPTEN5728phosphatase and tensin homolog
Click here to display 106 evidence detail records.
HumanPSEN15663presenilin 1
Click here to display 106 evidence detail records.
HumanPRODH5625proline dehydrogenase (oxidase) 1
Click here to display 106 evidence detail records.
HumanSEPT55413septin 5
Click here to display 106 evidence detail records.
HumanNPC14864Niemann-Pick disease, type C1
Click here to display 106 evidence detail records.
HumanMID14281midline 1 (Opitz/BBB syndrome)
Click here to display 106 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001488increased startle reflex0self