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Details
Link-It Detail - Jax Mouse Phenotype - increased blood osmolality
Debug Stats
  • ### Total Build Time: 96 ms 13.592 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 233 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 185 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=21 ms Completed: 21 ms rowSize= 580 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 1.579 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=51 ms Completed: 51 ms rowSize= 9.351 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
increased blood osmolality MP:0008997
Definition (1)
increase in the concentration of ions in the blood compared to the normal state
Synonyms (1)
"increased serum osmolality" NARROW
Parents (1)
img abnormal blood osmolality MP:0008996
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal blood osmolality MP:0008996
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
Click here to display 21 evidence detail records.
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
Click here to display 21 evidence detail records.
HumanVAMP88673vesicle-associated membrane protein 8
Click here to display 21 evidence detail records.
HumanTRPV17442transient receptor potential cation channel, subfamily V, member 1
Click here to display 21 evidence detail records.
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
Click here to display 21 evidence detail records.
HumanSLC2A26514solute carrier family 2 (facilitated glucose transporter), member 2
Click here to display 21 evidence detail records.
HumanRLN16013relaxin 1
Click here to display 21 evidence detail records.
HumanPLA2G4A5321phospholipase A2, group IVA (cytosolic, calcium-dependent)
Click here to display 21 evidence detail records.
HumanNOS24843nitric oxide synthase 2, inducible
Click here to display 21 evidence detail records.
HumanNOS14842nitric oxide synthase 1 (neuronal)
Click here to display 21 evidence detail records.
HumanKCNE13753potassium voltage-gated channel, Isk-related family, member 1
Click here to display 21 evidence detail records.
HumanCLN31201ceroid-lipofuscinosis, neuronal 3
Click here to display 21 evidence detail records.
HumanAQP3360aquaporin 3 (Gill blood group)
Click here to display 21 evidence detail records.
HumanAQP2359aquaporin 2 (collecting duct)
Click here to display 21 evidence detail records.
HumanAQP1358aquaporin 1
Click here to display 21 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008997increased blood osmolality0self