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Details
Link-It Detail - Jax Mouse Phenotype - abnormal head movements
Debug Stats
  • ### Total Build Time: 23 ms 20.460 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 274 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 180 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=3 ms Completed: 3 ms rowSize= 583 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.869 KB
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  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 14.326 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.161 KB
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Jax Mouse Phenotype (1)
abnormal head movements MP:0000436
Definition (1)
any anomaly in the motion of the portion of the body containing the brain and organs of sight, hearing, taste, and smell
Synonyms (1)
"abnormal head movement" EXACT
Parents (1)
img abnormal stationary movement MP:0001388
Children (4)
img head tossing MP:0005307
img head tilt MP:0005191
img head shaking MP:0002730
img head bobbing MP:0001410
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053867img abnormal stationary movement MP:0001388
Genes (75)

Species:
human : 75
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
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
HumanLRIG3121227leucine-rich repeats and immunoglobulin-like domains 3
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanESPN83715espin
INFERRED
HumanCDH2364072cadherin-related 23
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
Click here to display 15 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanBLOC1S455330biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino
INFERRED
HumanFIGN55137fidgetin
INFERRED
HumanCLIC553405chloride intracellular channel 5
INFERRED
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
HumanNOX350508NADPH oxidase 3
INFERRED
HumanBLOC1S626258biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
INFERRED
HumanDFNB3125861deafness, autosomal recessive 31
INFERRED
HumanATG4B23192autophagy related 4B, cysteine peptidase
INFERRED
HumanCACNG210369calcium channel, voltage-dependent, gamma subunit 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000436abnormal head movements0self