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Details
Link-It Detail - Jax Mouse Phenotype - impaired swimming
Debug Stats
  • ### Total Build Time: 667 ms 23.301 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 362 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 190 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 194 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=17 ms Completed: 17 ms rowSize= 1.034 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=18 ms Completed: 18 ms rowSize= 2.938 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=617 ms Completed: 617 ms rowSize= 17.292 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
impaired swimming MP:0001522
Definition (1)
reduced ability or inability to swim
Synonyms (1)
"impaired ability to orient in water" NARROW
Parents (2)
img abnormal locomotor coordination MP:0003312
img abnormal motor coordination/ balance MP:0001516
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053868img abnormal locomotor coordination MP:0003312
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal motor coordination/ balance MP:0001516
Genes (57)

Species:
human : 57
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SpeciesGeneGeneIdGene NameEvidence
HumanDFNB59494513deafness, autosomal recessive 59
Click here to display 142 evidence detail records.
HumanTBX10347853T-box 10
Click here to display 142 evidence detail records.
HumanOTOG340990otogelin
Click here to display 142 evidence detail records.
HumanTMIE259236transmembrane inner ear
Click here to display 142 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
Click here to display 142 evidence detail records.
HumanSPRED1161742sprouty-related, EVH1 domain containing 1
Click here to display 142 evidence detail records.
HumanOTOP1133060otopetrin 1
Click here to display 142 evidence detail records.
HumanSEZ6124925seizure related 6 homolog (mouse)
Click here to display 142 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
Click here to display 142 evidence detail records.
HumanESPN83715espin
Click here to display 142 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 142 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 142 evidence detail records.
HumanBLOC1S563915biogenesis of lysosomal organelles complex-1, subunit 5, muted
Click here to display 142 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 142 evidence detail records.
HumanMCOLN355283mucolipin 3
Click here to display 142 evidence detail records.
HumanCLIC553405chloride intracellular channel 5
Click here to display 142 evidence detail records.
HumanNOX350508NADPH oxidase 3
Click here to display 142 evidence detail records.
HumanDBNL28988drebrin-like
Click here to display 142 evidence detail records.
HumanGIT128964G protein-coupled receptor kinase interacting ArfGAP 1
Click here to display 142 evidence detail records.
HumanDFNB3125861deafness, autosomal recessive 31
Click here to display 142 evidence detail records.
HumanZDHHC1723390zinc finger, DHHC-type containing 17
Click here to display 142 evidence detail records.
HumanATG4B23192autophagy related 4B, cysteine peptidase
Click here to display 142 evidence detail records.
HumanCACNG210369calcium channel, voltage-dependent, gamma subunit 2
Click here to display 142 evidence detail records.
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
Click here to display 142 evidence detail records.
HumanNREP9315neuronal regeneration related protein
Click here to display 142 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001522impaired swimming0self