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Details
Link-It Detail - Jax Mouse Phenotype - abnormal skeleton physiology
Debug Stats
  • ### Total Build Time: 322 ms 23.479 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 210 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 197 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 573 bytes
  • CONCEPT_CHILDREN gt=21 ms Completed: 21 ms rowSize= 4.160 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.559 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=275 ms Completed: 275 ms rowSize= 15.117 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal skeleton physiology MP:0001533
Definition (1)
any functional anomaly of the bony framework of the body
Synonyms (1)
"bone/ skeletal physiology abnormalities" EXACT
Parents (1)
img skeleton phenotype MP:0005390
Children (9)
img abnormal chondrocyte physiology MP:0009780
img abnormal bone ossification MP:0008271
img abnormal bone strength MP:0001542
img abnormal bone remodeling MP:0002998
img osteomyelitis MP:0005190
img joint inflammation MP:0002933
img abnormal joint mobility MP:0008069
img abnormal bone healing MP:0002999
img abnormal tendon stiffness MP:0003097
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053903img skeleton phenotype MP:0005390
Genes (480)

Species:
human : 480
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanMIA3375056melanoma inhibitory activity family, member 3
INFERRED
HumanRSPO2340419R-spondin 2
INFERRED
HumanSIGLEC15284266sialic acid binding Ig-like lectin 15
INFERRED
HumanATP6V0D2245972ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2
INFERRED
HumanGPRC6A222545G protein-coupled receptor, family C, group 6, member A
INFERRED
HumanANO6196527anoctamin 6
INFERRED
HumanTMEM64169200transmembrane protein 64
INFERRED
HumanPHOSPHO1162466phosphatase, orphan 1
INFERRED
HumanFREM1158326FRAS1 related extracellular matrix 1
INFERRED
HumanAMER1139285APC membrane recruitment protein 1
INFERRED
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
INFERRED
HumanEVC2132884Ellis van Creveld syndrome 2
INFERRED
HumanOSR1130497odd-skipped related 1 (Drosophila)
INFERRED
HumanSP7121340Sp7 transcription factor
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
INFERRED
HumanCTHRC1115908collagen triple helix repeat containing 1
INFERRED
HumanRASGRP4115727RAS guanyl releasing protein 4
INFERRED
HumanPGLYRP2114770peptidoglycan recognition protein 2
INFERRED
HumanIL17F112744interleukin 17F
INFERRED
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001533abnormal skeleton physiology0self