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Details
Link-It Detail - Jax Mouse Phenotype - abnormal bone remodeling
Debug Stats
  • ### Total Build Time: 110 ms 21.344 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=10 ms Completed: 10 ms rowSize= 583 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 1.955 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.568 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=89 ms Completed: 89 ms rowSize= 15.250 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal bone remodeling MP:0002998
Definition (1)
aberrant process of the continuous turnover of bone matrix and mineral that involves a balance of resorption and reactive bone formation by osteoclasts and osteoblasts, respectively
Parents (1)
img abnormal skeleton physiology MP:0001533
Children (4)
img abnormal osteoblast physiology MP:0005006
img abnormal osteoclast physiology MP:0001541
img abnormal ossification involved in bone remodeling MP:0011720
img abnormal bone resorption MP:0004945
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053904img abnormal skeleton physiology MP:0001533
Genes (142)

Species:
human : 142
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
INFERRED
HumanANO6196527anoctamin 6
INFERRED
HumanTMEM64169200transmembrane protein 64
INFERRED
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
INFERRED
HumanCTHRC1115908collagen triple helix repeat containing 1
INFERRED
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
INFERRED
HumanDCSTAMP81501dendrocyte expressed seven transmembrane protein
INFERRED
HumanHIVEP359269human immunodeficiency virus type I enhancer binding protein 3
INFERRED
HumanSMURF157154SMAD specific E3 ubiquitin protein ligase 1
INFERRED
HumanMEPE56955matrix extracellular phosphoglycoprotein
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanFBLIM154751filamin binding LIM protein 1
INFERRED
HumanIL20RA53832interleukin 20 receptor, alpha
INFERRED
HumanWWOX51741WW domain containing oxidoreductase
INFERRED
HumanSUCO51430SUN domain containing ossification factor
Click here to display 37 evidence detail records.
HumanCLDN1851208claudin 18
INFERRED
HumanPLEKHO151177pleckstrin homology domain containing, family O member 1
INFERRED
HumanSOST50964sclerostin
Click here to display 37 evidence detail records.
HumanCLEC2D29121C-type lectin domain family 2, member D
INFERRED
HumanOSTM128962osteopetrosis associated transmembrane protein 1
INFERRED
HumanSATB223314SATB homeobox 2
INFERRED
HumanIRAK311213interleukin-1 receptor-associated kinase 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002998abnormal bone remodeling0self