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Details
Link-It Detail - Jax Mouse Phenotype - abnormal urine osmolality
Debug Stats
  • ### Total Build Time: 128 ms 21.230 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 225 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 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=11 ms Completed: 11 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=40 ms Completed: 40 ms rowSize= 1.021 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.924 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=47 ms Completed: 47 ms rowSize= 14.643 KB
  • CONCEPT_XREFS gt=13 ms Completed: 13 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal urine osmolality MP:0002987
Definition (1)
changes in the amount of ions in the urine compared to the normal state
Synonyms (1)
"abnormal urine osmolarity" EXACT
Parents (1)
img abnormal urine homeostasis MP:0009643
Children (2)
img decreased urine osmolality MP:0002988
img increased urine osmolality MP:0008055
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal urine homeostasis MP:0009643
img mammalian phenotype MP:0000001img renal/urinary system phenotype MP:00053675img abnormal urine homeostasis MP:0009643
Genes (58)

Species:
human : 58
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanAQP11282679aquaporin 11
INFERRED
HumanSLC26A7115111solute carrier family 26 (anion exchanger), member 7
INFERRED
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanTMEM2757393transmembrane protein 27
INFERRED
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
INFERRED
HumanFERMT155612fermitin family member 1
INFERRED
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
Click here to display 9 evidence detail records.
HumanLIN7C55327lin-7 homolog C (C. elegans)
INFERRED
HumanWWTR125937WW domain containing transcription regulator 1
INFERRED
HumanSIRT123411sirtuin 1
INFERRED
HumanOXSR19943oxidative stress responsive 1
INFERRED
HumanCLDN29075claudin 2
INFERRED
HumanCLDN109071claudin 10
INFERRED
HumanVAMP88673vesicle-associated membrane protein 8
INFERRED
HumanSLC4A48671solute carrier family 4 (sodium bicarbonate cotransporter), member 4
INFERRED
HumanSLC14A28170solute carrier family 14 (urea transporter), member 2
INFERRED
HumanIFT888100intraflagellar transport 88 homolog (Chlamydomonas)
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanUMOD7369uromodulin
Click here to display 9 evidence detail records.
HumanTGFB17040transforming growth factor, beta 1
INFERRED
HumanTFAP2B7021transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
INFERRED
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
INFERRED
HumanSLC5A26524solute carrier family 5 (sodium/glucose cotransporter), member 2
INFERRED
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
INFERRED
HumanSCTR6344secretin receptor
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002987abnormal urine osmolality0self