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Details
Link-It Detail - Jax Mouse Phenotype - decreased bone mineral content
Debug Stats
  • ### Total Build Time: 367 ms 21.333 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 246 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 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=13 ms Completed: 13 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=12 ms Completed: 12 ms rowSize= 1.569 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=329 ms Completed: 329 ms rowSize= 17.072 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
decreased bone mineral content MP:0010124
Definition (1)
reduction in the amount (usually in grams/cm) of bone mineral divided by a bone-scanned area
Synonyms (1)
"reduced bone mineral content" EXACT
Parents (1)
img abnormal bone mineral content MP:0010122
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053906img abnormal bone mineral content MP:0010122
Genes (38)

Species:
human : 38
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SpeciesGeneGeneIdGene NameEvidence
HumanTWSG157045twisted gastrulation homolog 1 (Drosophila)
Click here to display 120 evidence detail records.
HumanFAM20C56975family with sequence similarity 20, member C
Click here to display 120 evidence detail records.
HumanCLDN1851208claudin 18
Click here to display 120 evidence detail records.
HumanPRDM511107PR domain containing 5
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HumanMTSS19788metastasis suppressor 1
Click here to display 120 evidence detail records.
HumanSLC9A3R19368solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1
Click here to display 120 evidence detail records.
HumanUMOD7369uromodulin
Click here to display 120 evidence detail records.
HumanKLF107071Kruppel-like factor 10
Click here to display 120 evidence detail records.
HumanTHRA7067thyroid hormone receptor, alpha
Click here to display 120 evidence detail records.
HumanSMN26607survival of motor neuron 2, centromeric
Click here to display 120 evidence detail records.
HumanSMN16606survival of motor neuron 1, telomeric
Click here to display 120 evidence detail records.
HumanPTPN65777protein tyrosine phosphatase, non-receptor type 6
Click here to display 120 evidence detail records.
HumanPTPN25771protein tyrosine phosphatase, non-receptor type 2
Click here to display 120 evidence detail records.
HumanPYY5697peptide YY
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HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
Click here to display 120 evidence detail records.
HumanENPP15167ectonucleotide pyrophosphatase/phosphodiesterase 1
Click here to display 120 evidence detail records.
HumanDDR24921discoidin domain receptor tyrosine kinase 2
Click here to display 120 evidence detail records.
HumanMT1E4493metallothionein 1E
Click here to display 120 evidence detail records.
HumanKITLG4254KIT ligand
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HumanSMAD24087SMAD family member 2
Click here to display 120 evidence detail records.
HumanLRP24036low density lipoprotein receptor-related protein 2
Click here to display 120 evidence detail records.
HumanLMNA4000lamin A/C
Click here to display 120 evidence detail records.
HumanLAMC23918laminin, gamma 2
Click here to display 120 evidence detail records.
HumanIRS13667insulin receptor substrate 1
Click here to display 120 evidence detail records.
HumanIL103586interleukin 10
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010124decreased bone mineral content0self