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Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating potassium level
Debug Stats
  • ### Total Build Time: 80 ms 22.867 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 bytes
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  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.043 KB
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  • CONCEPT_GENES gt=39 ms Completed: 39 ms rowSize= 14.203 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal circulating potassium level MP:0002668
Definition (1)
anomalous concentration in the blood of this alkaline metallic element, the most abundant intracellular ion; anomalies in the extracellular (circulating) concentration have important implications for the function of excitable tissues, such as nerve and muscle
Synonyms (1)
"abnormal potassium level" EXACT
Parents (2)
img abnormal circulating mineral level MP:0006357
img abnormal potassium ion homeostasis MP:0011978
Children (2)
img decreased circulating potassium level MP:0005628
img increased circulating potassium level MP:0005627
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053767img abnormal circulating mineral level MP:0006357
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal circulating mineral level MP:0006357
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal potassium ion homeostasis MP:0011978
Genes (32)

Species:
human : 32
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanWNK465266WNK lysine deficient protein kinase 4
INFERRED
HumanFXYD453828FXYD domain containing ion transport regulator 4
INFERRED
HumanWWOX51741WW domain containing oxidoreductase
INFERRED
HumanRHCG51458Rh family, C glycoprotein
INFERRED
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
HumanSTK3927347serine threonine kinase 39
INFERRED
HumanZBTB2026137zinc finger and BTB domain containing 20
INFERRED
HumanNEDD4L23327neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
INFERRED
HumanTXNIP10628thioredoxin interacting protein
INFERRED
HumanOXSR19943oxidative stress responsive 1
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanTGFB17040transforming growth factor, beta 1
INFERRED
HumanSCNN1G6340sodium channel, non-voltage-gated 1, gamma subunit
INFERRED
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
INFERRED
HumanRYR16261ryanodine receptor 1 (skeletal)
INFERRED
HumanREN5972renin
INFERRED
HumanPOU3F35455POU class 3 homeobox 3
INFERRED
HumanPIK3C2A5286phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
INFERRED
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
INFERRED
HumanNR3C24306nuclear receptor subfamily 3, group C, member 2
INFERRED
HumanMC2R4158melanocortin 2 receptor (adrenocorticotropic hormone)
INFERRED
HumanKCNK33777potassium channel, subfamily K, member 3
INFERRED
HumanKCNE13753potassium voltage-gated channel, Isk-related family, member 1
INFERRED
HumanHSD11B23291hydroxysteroid (11-beta) dehydrogenase 2
INFERRED
HumanHNF4A3172hepatocyte nuclear factor 4, alpha
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002668abnormal circulating potassium level0self