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Details
Link-It Detail - Jax Mouse Phenotype - abnormal compact bone thickness
Debug Stats
  • ### Total Build Time: 46 ms 19.893 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 221 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=0 Completed: 0 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.033 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.572 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=40 ms Completed: 40 ms rowSize= 14.616 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal compact bone thickness MP:0000134
Definition (1)
reduced or increased width of the superficial layer of compact bone
Synonyms (1)
"abnormal cortical bone thickness" RELATED
Parents (1)
img abnormal compact bone morphology MP:0003797
Children (2)
img decreased compact bone thickness MP:0000135
img increased compact bone thickness MP:0004148
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053906img abnormal compact bone morphology MP:0003797
Genes (79)

Species:
human : 79
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPHOSPHO1162466phosphatase, orphan 1
INFERRED
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
INFERRED
HumanCREB3L190993cAMP responsive element binding protein 3-like 1
INFERRED
HumanSLC30A564924solute carrier family 30 (zinc transporter), member 5
INFERRED
HumanEBF264641early B-cell factor 2
INFERRED
HumanSMURF157154SMAD specific E3 ubiquitin protein ligase 1
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanWWOX51741WW domain containing oxidoreductase
INFERRED
HumanSUCO51430SUN domain containing ossification factor
INFERRED
HumanWNT1651384wingless-type MMTV integration site family, member 16
INFERRED
HumanCLDN1851208claudin 18
INFERRED
HumanSOST50964sclerostin
INFERRED
HumanCLEC2D29121C-type lectin domain family 2, member D
INFERRED
HumanIRAK311213interleukin-1 receptor-associated kinase 3
INFERRED
HumanAKR1A110327aldo-keto reductase family 1, member A1 (aldehyde reductase)
INFERRED
HumanTCIRG110312T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
INFERRED
HumanZMPSTE2410269zinc metallopeptidase STE24
INFERRED
HumanISG159636ISG15 ubiquitin-like modifier
INFERRED
HumanEIF2AK39451eukaryotic translation initiation factor 2-alpha kinase 3
INFERRED
HumanKL9365klotho
INFERRED
HumanTNFRSF11A8792tumor necrosis factor receptor superfamily, member 11a, NFKB activator
INFERRED
HumanTNFSF118600tumor necrosis factor (ligand) superfamily, member 11
INFERRED
HumanFZD98326frizzled family receptor 9
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000134abnormal compact bone thickness0self