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Details
Link-It Detail - Jax Mouse Phenotype - abnormal voluntary movement
Debug Stats
  • ### Total Build Time: 192 ms 21.549 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 260 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=0 Completed: 0 ms rowSize= 604 bytes
  • CONCEPT_CHILDREN gt=17 ms Completed: 17 ms rowSize= 2.332 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.602 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=165 ms Completed: 165 ms rowSize= 15.089 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal voluntary movement MP:0003491
Definition (1)
anomaly in coordinated movements executed with a purpose and can be improved by learning and/or experience
Parents (1)
img abnormal motor capabilities/coordination/movement MP:0002066
Children (5)
img abnormal stationary movement MP:0001388
img abnormal locomotor behavior MP:0001392
img spasticity MP:0012051
img paresis MP:0000754
img paralysis MP:0000753
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053865img abnormal motor capabilities/coordination/movement MP:0002066
Genes (1041)

Species:
human : 1041
Page Size
Current 25
  Page 1 of 42
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanCASP12100506742caspase 12 (gene/pseudogene)
INFERRED
HumanFOXO6100132074forkhead box O6
INFERRED
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanCBLN3643866cerebellin 3 precursor
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanSPRN503542shadow of prion protein homolog (zebrafish)
INFERRED
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanPLIN5440503perilipin 5
INFERRED
HumanBSX390259brain-specific homeobox
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanAGRN375790agrin
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanLRRTM1347730leucine rich repeat transmembrane neuronal 1
INFERRED
HumanNOTO344022notochord homeobox
INFERRED
HumanATXN1L342371ataxin 1-like
INFERRED
HumanOTOG340990otogelin
INFERRED
HumanHMX3340784H6 family homeobox 3
INFERRED
HumanNAT8L339983N-acetyltransferase 8-like (GCN5-related, putative)
INFERRED
HumanKY339855kyphoscoliosis peptidase
INFERRED
HumanDOK7285489docking protein 7
INFERRED
HumanPTRF284119polymerase I and transcript release factor
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003491abnormal voluntary movement0self