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Details
Link-It Detail - Jax Mouse Phenotype - paralysis
Debug Stats
  • ### Total Build Time: 143 ms 20.620 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 346 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 247 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.444 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=129 ms Completed: 129 ms rowSize= 15.156 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
paralysis MP:0000753
Definition (1)
loss of power of voluntary movement in a muscle through injury or disease of its nerve supply
Parents (1)
img abnormal voluntary movement MP:0003491
Children (3)
img carpoptosis MP:0005162
img hindlimb paralysis MP:0000755
img forelimb paralysis MP:0000756
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal voluntary movement MP:0003491
Genes (98)

Species:
human : 98
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNOTO344022notochord homeobox
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
Click here to display 82 evidence detail records.
HumanWNT3A89780wingless-type MMTV integration site family, member 3A
INFERRED
HumanPANK280025pantothenate kinase 2
INFERRED
HumanFA2H79152fatty acid 2-hydroxylase
INFERRED
HumanSCYL157410SCY1-like 1 (S. cerevisiae)
INFERRED
HumanMCOLN157192mucolipin 1
INFERRED
HumanTWSG157045twisted gastrulation homolog 1 (Drosophila)
INFERRED
HumanCOQ957017coenzyme Q9 homolog (S. cerevisiae)
INFERRED
HumanCLN654982ceroid-lipofuscinosis, neuronal 6, late infantile, variant
Click here to display 82 evidence detail records.
HumanVPS5451542vacuolar protein sorting 54 homolog (S. cerevisiae)
INFERRED
HumanDBNL28988drebrin-like
INFERRED
HumanLTN126046listerin E3 ubiquitin protein ligase 1
Click here to display 82 evidence detail records.
HumanTENM426011teneurin transmembrane protein 4
INFERRED
HumanFKBP823770FK506 binding protein 8, 38kDa
INFERRED
HumanSUZ1223512SUZ12 polycomb repressive complex 2 subunit
INFERRED
HumanGPR16123432G protein-coupled receptor 161
INFERRED
HumanNFASC23114neurofascin
Click here to display 82 evidence detail records.
HumanNMNAT223057nicotinamide nucleotide adenylyltransferase 2
Click here to display 82 evidence detail records.
HumanAFG3L210939AFG3 ATPase family member 3-like 2 (S. cerevisiae)
Click here to display 82 evidence detail records.
HumanAVIL10677advillin
INFERRED
HumanLBX110660ladybird homeobox 1
INFERRED
HumanTACC310460transforming, acidic coiled-coil containing protein 3
INFERRED
HumanNDRG110397N-myc downstream regulated 1
INFERRED
HumanNR1H310062nuclear receptor subfamily 1, group H, member 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000753paralysis0self