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Details
Link-It Detail - Jax Mouse Phenotype - abnormal blood osmolality
Debug Stats
  • ### Total Build Time: 10 ms 13.931 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 315 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=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.021 KB
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  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 8.597 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal blood osmolality MP:0008996
Definition (1)
anomaly in the concentration of ions in the blood or blood fractions compared to the normal state, sometimes reported as increased or decreased osmotic fragility
Synonyms (1)
"abnormal plasma osmolality" NARROW
Parents (1)
img abnormal blood homeostasis MP:0009642
Children (2)
img decreased blood osmolality MP:0008998
img increased blood osmolality MP:0008997
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal blood homeostasis MP:0009642
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
INFERRED
HumanSTEAP355240STEAP family member 3, metalloreductase
img Jax MP, Pubmed Id: 18617898, MOUSE PHENOTYPE ID: MGI:1915678
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
HumanVAMP88673vesicle-associated membrane protein 8
INFERRED
HumanTRPV17442transient receptor potential cation channel, subfamily V, member 1
INFERRED
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
INFERRED
HumanSLC2A26514solute carrier family 2 (facilitated glucose transporter), member 2
INFERRED
HumanRLN16013relaxin 1
INFERRED
HumanPLA2G4A5321phospholipase A2, group IVA (cytosolic, calcium-dependent)
INFERRED
HumanNOS24843nitric oxide synthase 2, inducible
INFERRED
HumanNOS14842nitric oxide synthase 1 (neuronal)
INFERRED
HumanKCNE13753potassium voltage-gated channel, Isk-related family, member 1
INFERRED
HumanCLN31201ceroid-lipofuscinosis, neuronal 3
INFERRED
HumanAQP3360aquaporin 3 (Gill blood group)
INFERRED
HumanAQP2359aquaporin 2 (collecting duct)
INFERRED
HumanAQP1358aquaporin 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008996abnormal blood osmolality0self