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Details
Link-It Detail - Jax Mouse Phenotype - abnormal compact bone morphology
Debug Stats
  • ### Total Build Time: 259 ms 22.851 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 392 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 324 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 177 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=22 ms Completed: 22 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= 578 bytes
  • CONCEPT_CHILDREN gt=23 ms Completed: 23 ms rowSize= 2.846 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.563 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=199 ms Completed: 199 ms rowSize= 15.690 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.170 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal compact bone morphology MP:0003797
Definition (1)
any structural anomaly of the outer layers of solid, hard bone that covers spongy bone; consists of parallel osteons containing mineral deposits and interstitial lamellae
Synonyms (1)
"abnormal dense bone" EXACT
Parents (1)
img abnormal bone structure MP:0003795
Children (6)
img abnormal compact bone mass MP:0010960
img absent compact bone MP:0010969
img abnormal compact bone thickness MP:0000134
img abnormal compact bone area MP:0010966
img abnormal compact bone volume MP:0010963
img abnormal compact bone lamellar structure MP:0010970
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal bone structure MP:0003795
Genes (115)

Species:
human : 115
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSIGLEC15284266sialic acid binding Ig-like lectin 15
INFERRED
HumanPHOSPHO1162466phosphatase, orphan 1
Click here to display 49 evidence detail records.
HumanAMER1139285APC membrane recruitment protein 1
Click here to display 49 evidence detail records.
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
HumanP2RY1353829purinergic receptor P2Y, G-protein coupled, 13
INFERRED
HumanWWOX51741WW domain containing oxidoreductase
Click here to display 49 evidence detail records.
HumanSUCO51430SUN domain containing ossification factor
Click here to display 49 evidence detail records.
HumanWNT1651384wingless-type MMTV integration site family, member 16
INFERRED
HumanCLDN1851208claudin 18
INFERRED
HumanSOST50964sclerostin
Click here to display 49 evidence detail records.
HumanRRM2B50484ribonucleotide reductase M2 B (TP53 inducible)
Click here to display 49 evidence detail records.
HumanANKRD1129123ankyrin repeat domain 11
INFERRED
HumanCLEC2D29121C-type lectin domain family 2, member D
INFERRED
HumanDICER123405dicer 1, ribonuclease type III
INFERRED
HumanIRAK311213interleukin-1 receptor-associated kinase 3
Click here to display 49 evidence detail records.
HumanPRDM511107PR domain containing 5
INFERRED
HumanAKR1A110327aldo-keto reductase family 1, member A1 (aldehyde reductase)
INFERRED
HumanTCIRG110312T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003797abnormal compact bone morphology0self