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Details
Link-It Detail - Jax Mouse Phenotype - paresis
Debug Stats
  • ### Total Build Time: 40 ms 15.179 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 342 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 261 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 175 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.580 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=33 ms Completed: 33 ms rowSize= 10.973 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
paresis MP:0000754
Definition (1)
partial loss of power of voluntary movement in a muscle through injury or disease of it or its nerve supply
Synonyms (1)
"partial paralysis" EXACT
Parents (1)
img abnormal voluntary movement MP:0003491
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal voluntary movement MP:0003491
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanSPTBN457731spectrin, beta, non-erythrocytic 4
Click here to display 35 evidence detail records.
HumanCLN654982ceroid-lipofuscinosis, neuronal 6, late infantile, variant
Click here to display 35 evidence detail records.
HumanDBNL28988drebrin-like
Click here to display 35 evidence detail records.
HumanSPG2023111spastic paraplegia 20 (Troyer syndrome)
Click here to display 35 evidence detail records.
HumanCNTNAP18506contactin associated protein 1
Click here to display 35 evidence detail records.
HumanVEGFA7422vascular endothelial growth factor A
Click here to display 35 evidence detail records.
HumanTTPA7274tocopherol (alpha) transfer protein
Click here to display 35 evidence detail records.
HumanPEX55830peroxisomal biogenesis factor 5
Click here to display 35 evidence detail records.
HumanPTPN95780protein tyrosine phosphatase, non-receptor type 9
Click here to display 35 evidence detail records.
HumanNRCAM4897neuronal cell adhesion molecule
Click here to display 35 evidence detail records.
HumanNOTCH34854notch 3
Click here to display 35 evidence detail records.
HumanLAMA23908laminin, alpha 2
Click here to display 35 evidence detail records.
HumanCCR102826chemokine (C-C motif) receptor 10
Click here to display 35 evidence detail records.
HumanGALC2581galactosylceramidase
Click here to display 35 evidence detail records.
HumanCLN82055ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
Click here to display 35 evidence detail records.
HumanCX3CR11524chemokine (C-X3-C motif) receptor 1
Click here to display 35 evidence detail records.
HumanCDKN1B1027cyclin-dependent kinase inhibitor 1B (p27, Kip1)
Click here to display 35 evidence detail records.
HumanCD86942CD86 molecule
Click here to display 35 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000754paresis0self