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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vestibuloocular dark reflex
Debug Stats
  • ### Total Build Time: 61 ms 18.272 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 294 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 171 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=9 ms Completed: 9 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=23 ms Completed: 23 ms rowSize= 4.285 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 11.244 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal vestibuloocular dark reflex MP:0011039
Definition (1)
any anomaly in the nystagmus or deviation of the eyes in response to stimulation of the vestibular system when the test is run without light
Synonyms (1)
"abnormal VORD" EXACT
Parents (1)
img abnormal vestibuloocular reflex MP:0004844
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053867img abnormal vestibuloocular reflex MP:0004844
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053868img abnormal vestibuloocular reflex MP:0004844
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal vestibuloocular reflex MP:0004844
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanTMC1117531transmembrane channel-like 1
img Jax MP, Pubmed Id: 18833191, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
img Jax MP, Pubmed Id: 22252133, MOUSE PHENOTYPE ID: MGI:1862037
HumanSLC12A557468solute carrier family 12 (potassium/chloride transporter), member 5
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
img Jax MP, Pubmed Id: 22252133, MOUSE PHENOTYPE ID: MGI:1862037
img Jax MP, Pubmed Id: 18833191, MOUSE PHENOTYPE ID: MGI:2153465
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img Jax MP, Pubmed Id: 18833191, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
img Jax MP, Pubmed Id: 22252133, MOUSE PHENOTYPE ID: MGI:1862037
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011039abnormal vestibuloocular dark reflex0self