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 - Human Phenotype - Abnormal middle ear reflexes
Debug Stats
  • ### Total Build Time: 73 ms 15.499 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 793 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.107 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=28 ms Completed: 28 ms rowSize= 3.979 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 8.272 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal middle ear reflexes HP:0004454
Parents (2)
img Abnormality of the middle ear HP:0000370
img Functional abnormality of the middle ear HP:0011452
Children (3)
img Absence of acoustic middle ear muscle reflexes HP:0008595
img Abnormal vestibulo-ocular reflex HP:0007670
img Absence of acoustic reflex HP:0008529
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the middle ear HP:0000370
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the middle ear HP:0000370
img All HP:0000001img Phenotypic abnormality HP:00001186img Functional abnormality of the middle ear HP:0011452
img All HP:0000001img Phenotypic abnormality HP:00001188img Functional abnormality of the middle ear HP:0011452
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanAUNX1751798auditory neuropathy, X-linked recessive 1
img HP TAS, OMIM ID: 300614
HumanNYS4317685nystagmus 4, congenital autosomal dominant
img HP RolledUp, OMIM ID: 193003
HumanESPN83715espin
img HP RolledUp, OMIM ID: 609006
HumanDIAPH381624diaphanous-related formin 3
img HP RolledUp, OMIM ID: 609129
HumanOTOF9381otoferlin
img HP RolledUp, OMIM ID: 601071
HumanAAAS8086achalasia, adrenocortical insufficiency, alacrimia
img HP RolledUp, OMIM ID: 231550
HumanUSH1E7396Usher syndrome 1E (autosomal recessive, severe)
img HP RolledUp, OMIM ID: 602097
HumanTGFBR17046transforming growth factor, beta receptor 1
img HP RolledUp, OMIM ID: 609129
HumanMYO7A4647myosin VIIA
img HP RolledUp, OMIM ID: 276903
HumanCACNA1A773calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
img HP RolledUp, OMIM ID: 183086
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004454Abnormal middle ear reflexes0self