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Details
Link-It Detail - Jax Mouse Phenotype - abnormal potassium ion homeostasis
Debug Stats
  • ### Total Build Time: 18 ms 19.635 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 396 bytes
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  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal potassium ion homeostasis MP:0011978
Definition (1)
anomaly in the processes involved in the maintenance of an internal equilibrium of potassium ions within the body or between a cell and its external environment
Parents (1)
img abnormal ion homeostasis MP:0001765
Children (2)
img abnormal circulating potassium level MP:0002668
img abnormal urine potassium level MP:0004820
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal ion homeostasis MP:0001765
Genes (55)

Species:
human : 55
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanWNK465266WNK lysine deficient protein kinase 4
INFERRED
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
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
HumanTFCP2L129842transcription factor CP2-like 1
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
HumanDKK122943dickkopf WNT signaling pathway inhibitor 1
INFERRED
HumanTXNIP10628thioredoxin interacting protein
INFERRED
HumanVAV310451vav 3 guanine nucleotide exchange factor
INFERRED
HumanOXSR19943oxidative stress responsive 1
INFERRED
HumanADAMTS19510ADAM metallopeptidase with thrombospondin type 1 motif, 1
INFERRED
HumanCLDN109071claudin 10
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED
HumanUPK27379uroplakin 2
INFERRED
HumanUMOD7369uromodulin
INFERRED
HumanTGFB17040transforming growth factor, beta 1
INFERRED
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
INFERRED
HumanSLC5A26524solute carrier family 5 (sodium/glucose cotransporter), member 2
INFERRED
HumanSLC5A16523solute carrier family 5 (sodium/glucose cotransporter), member 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011978abnormal potassium ion homeostasis0self