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Details
Link-It Detail - Jax Mouse Phenotype - abnormal locomotor coordination
Debug Stats
  • ### Total Build Time: 88 ms 22.023 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 290 bytes
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  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.773 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.580 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=82 ms Completed: 82 ms rowSize= 15.124 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.169 KB
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Jax Mouse Phenotype (1)
abnormal locomotor coordination MP:0003312
Definition (1)
reduced ability of an animal to maintain skillful and effective interaction of movements while engaging in behavioral locomotor activity
Parents (1)
img abnormal locomotor behavior MP:0001392
Children (6)
img athetotic walking movements MP:0001527
img weaving MP:0008913
img impaired swimming MP:0001522
img impaired limb coordination MP:0001524
img ataxia MP:0001393
img abnormal gait MP:0001406
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053867img abnormal locomotor behavior MP:0001392
Genes (460)

Species:
human : 460
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanCASP12100506742caspase 12 (gene/pseudogene)
Click here to display 65 evidence detail records.
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanCBLN3643866cerebellin 3 precursor
INFERRED
HumanSPRN503542shadow of prion protein homolog (zebrafish)
INFERRED
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanOTOG340990otogelin
INFERRED
HumanKY339855kyphoscoliosis peptidase
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanSPRED1161742sprouty-related, EVH1 domain containing 1
INFERRED
HumanTTL150465tubulin tyrosine ligase
INFERRED
HumanLIPI149998lipase, member I
INFERRED
HumanCLDN19149461claudin 19
INFERRED
HumanOTOP1133060otopetrin 1
INFERRED
HumanEDARADD128178EDAR-associated death domain
Click here to display 65 evidence detail records.
HumanSYT2127833synaptotagmin II
INFERRED
HumanSEZ6124925seizure related 6 homolog (mouse)
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanSTX1B112755syntaxin 1B
INFERRED
HumanZIC585416Zic family member 5
INFERRED
HumanATCAY85300ataxia, cerebellar, Cayman type
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003312abnormal locomotor coordination0self