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Details
Link-It Detail - Jax Mouse Phenotype - abnormal gait
Debug Stats
  • ### Total Build Time: 4,952 ms 23.275 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 293 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 171 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=4 ms Completed: 4 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.007 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.584 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=4,939 ms Completed: 4.939 Seconds rowSize= 18.018 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal gait MP:0001406
Definition (1)
abnormal pattern of movement of the limbs of animals, characterized by elements of progression, stability, speed and length over the ground
Synonyms (1)
"peculiar gait" EXACT
Parents (1)
img abnormal locomotor coordination MP:0003312
Children (2)
img short stride length MP:0001407
img long stride length MP:0010540
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053868img abnormal locomotor coordination MP:0003312
Genes (258)

Species:
human : 258
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanSKOR2652991SKI family transcriptional corepressor 2
Click here to display 647 evidence detail records.
HumanCBLN3643866cerebellin 3 precursor
Click here to display 647 evidence detail records.
HumanTBX10347853T-box 10
Click here to display 647 evidence detail records.
HumanKY339855kyphoscoliosis peptidase
Click here to display 647 evidence detail records.
HumanPTF1A256297pancreas specific transcription factor, 1a
Click here to display 647 evidence detail records.
HumanLIPI149998lipase, member I
Click here to display 647 evidence detail records.
HumanCLDN19149461claudin 19
Click here to display 647 evidence detail records.
HumanZIC585416Zic family member 5
Click here to display 647 evidence detail records.
HumanESPN83715espin
Click here to display 647 evidence detail records.
HumanJAM383700junctional adhesion molecule 3
Click here to display 647 evidence detail records.
HumanPREX280243phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2
INFERRED
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Click here to display 647 evidence detail records.
HumanPINK165018PTEN induced putative kinase 1
Click here to display 647 evidence detail records.
HumanCERK64781ceramide kinase
Click here to display 647 evidence detail records.
HumanEBF264641early B-cell factor 2
Click here to display 647 evidence detail records.
HumanMPP564398membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5)
Click here to display 647 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 647 evidence detail records.
HumanNPAS364067neuronal PAS domain protein 3
Click here to display 647 evidence detail records.
HumanSPTBN457731spectrin, beta, non-erythrocytic 4
Click here to display 647 evidence detail records.
HumanPRX57716periaxin
Click here to display 647 evidence detail records.
HumanKLHL157626kelch-like family member 1
Click here to display 647 evidence detail records.
HumanBAHCC157597BAH domain and coiled-coil containing 1
Click here to display 647 evidence detail records.
HumanSLC12A557468solute carrier family 12 (potassium/chloride transporter), member 5
Click here to display 647 evidence detail records.
HumanSCYL157410SCY1-like 1 (S. cerevisiae)
Click here to display 647 evidence detail records.
HumanMCOLN157192mucolipin 1
Click here to display 647 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001406abnormal gait0self