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Details
Link-It Detail - Jax Mouse Phenotype - increased blood uric acid level
Debug Stats
  • ### Total Build Time: 55 ms 10.705 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 394 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 187 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=11 ms Completed: 11 ms rowSize= 585 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.584 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 6.280 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
increased blood uric acid level MP:0008821
Definition (1)
greater concentration in the blood of the final oxidation product of purine catabolism in humans and primates, but which in rodents and most other mammals is normally is further oxidized by uricase to allantoin that is excreted in the urine
Synonyms (1)
"increased blood urate level" RELATED
Parents (1)
img abnormal blood uric acid level MP:0008820
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal blood uric acid level MP:0008820
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
Click here to display 16 evidence detail records.
HumanWWOX51741WW domain containing oxidoreductase
Click here to display 16 evidence detail records.
HumanDLL128514delta-like 1 (Drosophila)
Click here to display 16 evidence detail records.
HumanSPG2023111spastic paraplegia 20 (Troyer syndrome)
Click here to display 16 evidence detail records.
HumanUMOD7369uromodulin
Click here to display 16 evidence detail records.
HumanPXMP25827peroxisomal membrane protein 2, 22kDa
Click here to display 16 evidence detail records.
HumanPITX35309paired-like homeodomain 3
Click here to display 16 evidence detail records.
HumanLEPR3953leptin receptor
Click here to display 16 evidence detail records.
HumanG6PC2538glucose-6-phosphatase, catalytic subunit
Click here to display 16 evidence detail records.
HumanALB213albumin
Click here to display 16 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008821increased blood uric acid level0self