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Details
Link-It Detail - Jax Mouse Phenotype - abnormal bone mineral content
Debug Stats
  • ### Total Build Time: 51 ms 20.184 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 248 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 170 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=5 ms Completed: 5 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.029 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.563 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=30 ms Completed: 30 ms rowSize= 14.930 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal bone mineral content MP:0010122
Definition (1)
any anomaly in the amount (usually in grams/cm) of bone mineral divided by a bone-scanned area
Synonyms (1)
"abnormal BMC" EXACT
Parents (1)
img abnormal bone structure MP:0003795
Children (2)
img increased bone mineral content MP:0010123
img decreased bone mineral content MP:0010124
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal bone structure MP:0003795
Genes (57)

Species:
human : 57
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSIGLEC15284266sialic acid binding Ig-like lectin 15
INFERRED
HumanRICTOR253260RPTOR independent companion of MTOR, complex 2
INFERRED
HumanTMEM64169200transmembrane protein 64
INFERRED
HumanTWSG157045twisted gastrulation homolog 1 (Drosophila)
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanCLDN1851208claudin 18
INFERRED
HumanCHSY122856chondroitin sulfate synthase 1
img Jax MP, Pubmed Id: 22280990, MOUSE PHENOTYPE ID: MGI:2681120
HumanPRDM511107PR domain containing 5
INFERRED
HumanTCIRG110312T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
INFERRED
HumanHDAC610013histone deacetylase 6
INFERRED
HumanMTSS19788metastasis suppressor 1
INFERRED
HumanSLC9A3R19368solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1
INFERRED
HumanFGF238074fibroblast growth factor 23
INFERRED
HumanUMOD7369uromodulin
INFERRED
HumanTYROBP7305TYRO protein tyrosine kinase binding protein
INFERRED
HumanTLR47099toll-like receptor 4
INFERRED
HumanKLF107071Kruppel-like factor 10
INFERRED
HumanTHRA7067thyroid hormone receptor, alpha
INFERRED
HumanSMN26607survival of motor neuron 2, centromeric
INFERRED
HumanSMN16606survival of motor neuron 1, telomeric
INFERRED
HumanPTPN65777protein tyrosine phosphatase, non-receptor type 6
INFERRED
HumanPTPN35774protein tyrosine phosphatase, non-receptor type 3
INFERRED
HumanPTPN25771protein tyrosine phosphatase, non-receptor type 2
INFERRED
HumanPYY5697peptide YY
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010122abnormal bone mineral content0self