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Details
Link-It Detail - Jax Mouse Phenotype - abnormal motor coordination/ balance
Debug Stats
  • ### Total Build Time: 495 ms 24.909 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 272 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 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
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  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 604 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 5.451 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.602 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=486 ms Completed: 486 ms rowSize= 15.115 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal motor coordination/ balance MP:0001516
Definition (1)
altered ability of an animal to maintain skillful and effective interaction of movements or maintenance of equilibrium
Synonyms (1)
"impaired proprioception" EXACT
Parents (1)
img abnormal motor capabilities/coordination/movement MP:0002066
Children (12)
img abnormal placing response MP:0001526
img altered righting response MP:0002862
img ataxia MP:0001393
img impaired coordination MP:0001405
img jerky movement MP:0005424
img athetotic walking movements MP:0001527
img dysmetria MP:0003314
img enhanced coordination MP:0003858
img impaired swimming MP:0001522
img impaired limb coordination MP:0001524
img impaired balance MP:0001525
img jumpy MP:0001401
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053865img abnormal motor capabilities/coordination/movement MP:0002066
Genes (613)

Species:
human : 613
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanTIMM23100287932translocase of inner mitochondrial membrane 23 homolog (yeast)
INFERRED
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanCBLN3643866cerebellin 3 precursor
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanSPRN503542shadow of prion protein homolog (zebrafish)
INFERRED
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED
HumanCCL3L3414062chemokine (C-C motif) ligand 3-like 3
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanBARHL2343472BarH-like homeobox 2
INFERRED
HumanOTOG340990otogelin
INFERRED
HumanHMX3340784H6 family homeobox 3
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
Click here to display 170 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED
HumanARX170302aristaless related homeobox
INFERRED
HumanLGI4163175leucine-rich repeat LGI family, member 4
INFERRED
HumanSPRED1161742sprouty-related, EVH1 domain containing 1
INFERRED
HumanTTL150465tubulin tyrosine ligase
INFERRED
HumanCLDN19149461claudin 19
INFERRED
HumanOTOP1133060otopetrin 1
INFERRED
HumanSYT2127833synaptotagmin II
INFERRED
HumanSEZ6124925seizure related 6 homolog (mouse)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001516abnormal motor coordination/ balance0self