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Details
Link-It Detail - Jax Mouse Phenotype - kidney degeneration
Debug Stats
  • ### Total Build Time: 30 ms 20.313 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 341 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 176 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=4 ms Completed: 4 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 571 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.578 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 15.446 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
kidney degeneration MP:0009641
Definition (1)
a retrogressive impairment of function or destruction of either or both of the two excretory organs that filter wastes (especially urea) from the blood and excrete them and water in urine
Synonyms (1)
"renal degeneration" EXACT
Parents (1)
img abnormal kidney morphology MP:0002135
Children (1)
img renal necrosis MP:0003946
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img renal/urinary system phenotype MP:00053675img abnormal kidney morphology MP:0002135
Genes (39)

Species:
human : 39
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
Click here to display 17 evidence detail records.
HumanGLIS284662GLIS family zinc finger 2
Click here to display 17 evidence detail records.
HumanKIF26B55083kinesin family member 26B
Click here to display 17 evidence detail records.
HumanCRIM151232cysteine rich transmembrane BMP regulator 1 (chordin-like)
INFERRED
HumanRRM2B50484ribonucleotide reductase M2 B (TP53 inducible)
INFERRED
HumanTREX111277three prime repair exonuclease 1
INFERRED
HumanSLC7A911136solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
INFERRED
HumanMTSS19788metastasis suppressor 1
Click here to display 17 evidence detail records.
HumanVAMP88673vesicle-associated membrane protein 8
Click here to display 17 evidence detail records.
HumanNPHS27827nephrosis 2, idiopathic, steroid-resistant (podocin)
INFERRED
HumanTNS17145tensin 1
Click here to display 17 evidence detail records.
HumanTLR47099toll-like receptor 4
INFERRED
HumanTGFB17040transforming growth factor, beta 1
INFERRED
HumanSPTB6710spectrin, beta, erythrocytic
INFERRED
HumanSPTA16708spectrin, alpha, erythrocytic 1 (elliptocytosis 2)
INFERRED
HumanSPP16696secreted phosphoprotein 1
INFERRED
HumanSDC46385syndecan 4
Click here to display 17 evidence detail records.
HumanSALL16299sal-like 1 (Drosophila)
INFERRED
HumanPTGS25743prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
Click here to display 17 evidence detail records.
HumanPTGIS5740prostaglandin I2 (prostacyclin) synthase
INFERRED
HumanPKHD15314polycystic kidney and hepatic disease 1 (autosomal recessive)
INFERRED
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
Click here to display 17 evidence detail records.
HumanNOS14842nitric oxide synthase 1 (neuronal)
INFERRED
HumanMXI14601MAX interactor 1, dimerization protein
Click here to display 17 evidence detail records.
HumanMT1E4493metallothionein 1E
Click here to display 17 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009641kidney degeneration0self