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Details
Link-It Detail - Jax Mouse Phenotype - decreased urine osmolality
Debug Stats
  • ### Total Build Time: 196 ms 22.850 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 227 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 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=5 ms Completed: 5 ms rowSize= 580 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.922 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=180 ms Completed: 180 ms rowSize= 17.274 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
decreased urine osmolality MP:0002988
Definition (1)
reduction in the amount of ions in the urine compared to the normal state
Synonyms (1)
"reduced urine osmolality" EXACT
Parents (1)
img abnormal urine osmolality MP:0002987
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal urine osmolality MP:0002987
img mammalian phenotype MP:0000001img renal/urinary system phenotype MP:00053676img abnormal urine osmolality MP:0002987
Genes (50)

Species:
human : 50
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanAQP11282679aquaporin 11
Click here to display 97 evidence detail records.
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
Click here to display 97 evidence detail records.
HumanTMEM2757393transmembrane protein 27
Click here to display 97 evidence detail records.
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
Click here to display 97 evidence detail records.
HumanLIN7C55327lin-7 homolog C (C. elegans)
Click here to display 97 evidence detail records.
HumanWWTR125937WW domain containing transcription regulator 1
Click here to display 97 evidence detail records.
HumanSIRT123411sirtuin 1
Click here to display 97 evidence detail records.
HumanOXSR19943oxidative stress responsive 1
Click here to display 97 evidence detail records.
HumanCLDN29075claudin 2
Click here to display 97 evidence detail records.
HumanCLDN109071claudin 10
Click here to display 97 evidence detail records.
HumanVAMP88673vesicle-associated membrane protein 8
Click here to display 97 evidence detail records.
HumanSLC4A48671solute carrier family 4 (sodium bicarbonate cotransporter), member 4
Click here to display 97 evidence detail records.
HumanSLC14A28170solute carrier family 14 (urea transporter), member 2
Click here to display 97 evidence detail records.
HumanIFT888100intraflagellar transport 88 homolog (Chlamydomonas)
Click here to display 97 evidence detail records.
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Click here to display 97 evidence detail records.
HumanUMOD7369uromodulin
Click here to display 97 evidence detail records.
HumanTGFB17040transforming growth factor, beta 1
Click here to display 97 evidence detail records.
HumanTFAP2B7021transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
Click here to display 97 evidence detail records.
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
Click here to display 97 evidence detail records.
HumanSLC5A26524solute carrier family 5 (sodium/glucose cotransporter), member 2
Click here to display 97 evidence detail records.
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
Click here to display 97 evidence detail records.
HumanSCTR6344secretin receptor
Click here to display 97 evidence detail records.
HumanREN5972renin
Click here to display 97 evidence detail records.
HumanPTGER15731prostaglandin E receptor 1 (subtype EP1), 42kDa
Click here to display 97 evidence detail records.
HumanPPP3CA5530protein phosphatase 3, catalytic subunit, alpha isozyme
Click here to display 97 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002988decreased urine osmolality0self