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Details
Link-It Detail - Jax Mouse Phenotype - head tossing
Debug Stats
  • ### Total Build Time: 207 ms 18.618 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 352 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 208 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=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=15 ms Completed: 15 ms rowSize= 1.011 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=21 ms Completed: 21 ms rowSize= 2.915 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=156 ms Completed: 156 ms rowSize= 12.843 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
head tossing MP:0005307
Definition (1)
repetitive flailing of the head in multiple directions
Parents (2)
img abnormal head movements MP:0000436
img stereotypic behavior MP:0001408
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053868img abnormal head movements MP:0000436
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img stereotypic behavior MP:0001408
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 86 evidence detail records.
HumanTBX10347853T-box 10
Click here to display 86 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
Click here to display 86 evidence detail records.
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
Click here to display 86 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
Click here to display 86 evidence detail records.
HumanLRIG3121227leucine-rich repeats and immunoglobulin-like domains 3
Click here to display 86 evidence detail records.
HumanSRRM484530serine/arginine repetitive matrix 4
Click here to display 86 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 86 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 86 evidence detail records.
HumanCACNG210369calcium channel, voltage-dependent, gamma subunit 2
Click here to display 86 evidence detail records.
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
Click here to display 86 evidence detail records.
HumanSOX26657SRY (sex determining region Y)-box 2
Click here to display 86 evidence detail records.
HumanSLC12A26558solute carrier family 12 (sodium/potassium/chloride transporter), member 2
Click here to display 86 evidence detail records.
HumanPOU4F35459POU class 4 homeobox 3
Click here to display 86 evidence detail records.
HumanMYO7A4647myosin VIIA
Click here to display 86 evidence detail records.
HumanMYO64646myosin VI
Click here to display 86 evidence detail records.
HumanLMX1A4009LIM homeobox transcription factor 1, alpha
Click here to display 86 evidence detail records.
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
Click here to display 86 evidence detail records.
HumanKCNE13753potassium voltage-gated channel, Isk-related family, member 1
Click here to display 86 evidence detail records.
HumanATF21386activating transcription factor 2
Click here to display 86 evidence detail records.
HumanATP2B2491ATPase, Ca++ transporting, plasma membrane 2
Click here to display 86 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005307head tossing0self