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Details
Link-It Detail - Jax Mouse Phenotype - abnormal osteoclast morphology
Debug Stats
  • ### Total Build Time: 347 ms 29.259 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 296 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 192 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=10 ms Completed: 10 ms rowSize= 1.021 KB
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.035 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 9.635 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=328 ms Completed: 328 ms rowSize= 15.400 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal osteoclast morphology MP:0004982
Definition (1)
any structural anomaly of the specialized phagocytic cells associated with the absorption and removal of the mineralized matrix of bone tissue
Synonyms (1)
"abnormal chondroclast morphology" RELATED
Parents (2)
img abnormal macrophage morphology MP:0002446
img abnormal bone structure MP:0003795
Children (2)
img abnormal osteoclast cell number MP:0004983
img abnormal osteoclast differentiation MP:0008396
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img immune system phenotype MP:00053877img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053979img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img immune system phenotype MP:00053879img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:000539710img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img immune system phenotype MP:000538710img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:000539711img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal bone structure MP:0003795
Genes (138)

Species:
human : 138
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanSIGLEC15284266sialic acid binding Ig-like lectin 15
INFERRED
HumanATP6V0D2245972ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2
Click here to display 67 evidence detail records.
HumanTMEM64169200transmembrane protein 64
INFERRED
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
INFERRED
HumanOSCAR126014osteoclast associated, immunoglobulin-like receptor
INFERRED
HumanJDP2122953Jun dimerization protein 2
Click here to display 67 evidence detail records.
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
INFERRED
HumanDCSTAMP81501dendrocyte expressed seven transmembrane protein
INFERRED
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanIL17RB55540interleukin 17 receptor B
INFERRED
HumanFBLIM154751filamin binding LIM protein 1
INFERRED
HumanIL20RA53832interleukin 20 receptor, alpha
INFERRED
HumanSUCO51430SUN domain containing ossification factor
INFERRED
HumanCLDN1851208claudin 18
INFERRED
HumanANKRD1129123ankyrin repeat domain 11
INFERRED
HumanCLEC2D29121C-type lectin domain family 2, member D
INFERRED
HumanDKK227123dickkopf WNT signaling pathway inhibitor 2
INFERRED
HumanIRAK311213interleukin-1 receptor-associated kinase 3
INFERRED
HumanHCST10870hematopoietic cell signal transducer
INFERRED
HumanTOB210766transducer of ERBB2, 2
INFERRED
HumanAKR1A110327aldo-keto reductase family 1, member A1 (aldehyde reductase)
INFERRED
HumanTCIRG110312T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
Click here to display 67 evidence detail records.
HumanWDR19948WD repeat domain 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004982abnormal osteoclast morphology0self