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Details
Link-It Detail - Jax Mouse Phenotype - abnormal stationary movement
Debug Stats
  • ### Total Build Time: 110 ms 21.484 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 226 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=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=0 Completed: 0 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 1.902 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=85 ms Completed: 85 ms rowSize= 15.356 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal stationary movement MP:0001388
Definition (1)
altered ability or inability to change body posture or shift a body part
Synonyms (1)
"abnormal movement" EXACT
Parents (1)
img abnormal voluntary movement MP:0003491
Children (4)
img abnormal tail movements MP:0001391
img bradykinesia MP:0005156
img abnormal head movements MP:0000436
img abnormal eye movement MP:0001389
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal voluntary movement MP:0003491
Genes (140)

Species:
human : 140
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanOTOG340990otogelin
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanOTOP1133060otopetrin 1
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanNOXO1124056NADPH oxidase organizer 1
INFERRED
HumanNTAN1123803N-terminal asparagine amidase
INFERRED
HumanLRIG3121227leucine-rich repeats and immunoglobulin-like domains 3
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanOPN494233opsin 4
INFERRED
HumanFOXP293986forkhead box P2
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanESPN83715espin
Click here to display 34 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 34 evidence detail records.
HumanBAHCC157597BAH domain and coiled-coil containing 1
INFERRED
HumanUNC7957578unc-79 homolog (C. elegans)
INFERRED
HumanSCYL157410SCY1-like 1 (S. cerevisiae)
Click here to display 34 evidence detail records.
HumanVANGL257216VANGL planar cell polarity protein 2
INFERRED
HumanDIABLO56616diablo, IAP-binding mitochondrial protein
Click here to display 34 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 34 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001388abnormal stationary movement0self