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Details
Link-It Detail - Jax Mouse Phenotype - renal interstitial fibrosis
Debug Stats
  • ### Total Build Time: 161 ms 23.192 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 310 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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=3 ms Completed: 3 ms rowSize= 1.021 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.923 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=152 ms Completed: 152 ms rowSize= 17.256 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
renal interstitial fibrosis MP:0003215
Definition (1)
formation of fibrous tissue within the functional space in the kidney beneath the individual filters (glomeruli) as a result of repair or a reactive process
Parents (2)
img renal fibrosis MP:0003985
img abnormal kidney interstitium morphology MP:0011425
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img renal/urinary system phenotype MP:00053676img renal fibrosis MP:0003985
img mammalian phenotype MP:0000001img renal/urinary system phenotype MP:00053676img abnormal kidney interstitium morphology MP:0011425
Genes (42)

Species:
human : 42
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanKCP375616kielin/chordin-like protein
Click here to display 74 evidence detail records.
HumanGLIS284662GLIS family zinc finger 2
Click here to display 74 evidence detail records.
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
Click here to display 74 evidence detail records.
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
Click here to display 74 evidence detail records.
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
Click here to display 74 evidence detail records.
HumanLIN7C55327lin-7 homolog C (C. elegans)
Click here to display 74 evidence detail records.
HumanCRIM151232cysteine rich transmembrane BMP regulator 1 (chordin-like)
Click here to display 74 evidence detail records.
HumanNPHP327031nephronophthisis 3 (adolescent)
Click here to display 74 evidence detail records.
HumanWWTR125937WW domain containing transcription regulator 1
Click here to display 74 evidence detail records.
HumanKIF3A11127kinesin family member 3A
Click here to display 74 evidence detail records.
HumanGRHPR9380glyoxylate reductase/hydroxypyruvate reductase
Click here to display 74 evidence detail records.
HumanNPHS27827nephrosis 2, idiopathic, steroid-resistant (podocin)
Click here to display 74 evidence detail records.
HumanXDH7498xanthine dehydrogenase
Click here to display 74 evidence detail records.
HumanWT17490Wilms tumor 1
Click here to display 74 evidence detail records.
HumanVHL7428von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
Click here to display 74 evidence detail records.
HumanTNFRSF1B7133tumor necrosis factor receptor superfamily, member 1B
Click here to display 74 evidence detail records.
HumanREN5972renin
Click here to display 74 evidence detail records.
HumanPTGS25743prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
Click here to display 74 evidence detail records.
HumanLGMN5641legumain
Click here to display 74 evidence detail records.
HumanPPP3R15534protein phosphatase 3, regulatory subunit B, alpha
Click here to display 74 evidence detail records.
HumanPKHD15314polycystic kidney and hepatic disease 1 (autosomal recessive)
Click here to display 74 evidence detail records.
HumanPKD15310polycystic kidney disease 1 (autosomal dominant)
Click here to display 74 evidence detail records.
HumanMYO1E4643myosin IE
Click here to display 74 evidence detail records.
HumanMT1E4493metallothionein 1E
Click here to display 74 evidence detail records.
HumanMPV174358MpV17 mitochondrial inner membrane protein
Click here to display 74 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003215renal interstitial fibrosis0self