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Details
Link-It Detail - Jax Mouse Phenotype - impaired limb coordination
Debug Stats
  • ### Total Build Time: 361 ms 23.130 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 242 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=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=8 ms Completed: 8 ms rowSize= 1.034 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.938 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=339 ms Completed: 339 ms rowSize= 17.233 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
impaired limb coordination MP:0001524
Definition (1)
reduced ability to organize limb movements to execute complex maneuvers, such as walking
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 (43)

Species:
human : 43
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanGPR12657211G protein-coupled receptor 126
Click here to display 109 evidence detail records.
HumanLPIN123175lipin 1
Click here to display 109 evidence detail records.
HumanPARK711315parkinson protein 7
Click here to display 109 evidence detail records.
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
Click here to display 109 evidence detail records.
HumanMFN29927mitofusin 2
Click here to display 109 evidence detail records.
HumanGAL3ST19514galactose-3-O-sulfotransferase 1
Click here to display 109 evidence detail records.
HumanCNTNAP18506contactin associated protein 1
Click here to display 109 evidence detail records.
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
Click here to display 109 evidence detail records.
HumanZIC17545Zic family member 1
Click here to display 109 evidence detail records.
HumanTRPC37222transient receptor potential cation channel, subfamily C, member 3
Click here to display 109 evidence detail records.
HumanVAMP16843vesicle-associated membrane protein 1 (synaptobrevin 1)
Click here to display 109 evidence detail records.
HumanSPG76687spastic paraplegia 7 (pure and complicated autosomal recessive)
Click here to display 109 evidence detail records.
HumanSMN26607survival of motor neuron 2, centromeric
Click here to display 109 evidence detail records.
HumanSMN16606survival of motor neuron 1, telomeric
Click here to display 109 evidence detail records.
HumanSHC16464SHC (Src homology 2 domain containing) transforming protein 1
Click here to display 109 evidence detail records.
HumanPSAP5660prosaposin
Click here to display 109 evidence detail records.
HumanNTRK34916neurotrophic tyrosine kinase, receptor, type 3
Click here to display 109 evidence detail records.
HumanNTF34908neurotrophin 3
Click here to display 109 evidence detail records.
HumanMYL14632myosin, light chain 1, alkali; skeletal, fast
Click here to display 109 evidence detail records.
HumanMID14281midline 1 (Opitz/BBB syndrome)
Click here to display 109 evidence detail records.
HumanMEOX24223mesenchyme homeobox 2
Click here to display 109 evidence detail records.
HumanLAMA43910laminin, alpha 4
Click here to display 109 evidence detail records.
HumanL1CAM3897L1 cell adhesion molecule
Click here to display 109 evidence detail records.
HumanKCNN23781potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2
Click here to display 109 evidence detail records.
HumanKCNE13753potassium voltage-gated channel, Isk-related family, member 1
Click here to display 109 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001524impaired limb coordination0self