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Details
Link-It Detail - Jax Mouse Phenotype - alkalosis
Debug Stats
  • ### Total Build Time: 12 ms 28.852 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 346 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 420 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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
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  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 583 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.582 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 24.652 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.147 KB
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Jax Mouse Phenotype (1)
alkalosis MP:0003028
Definition (1)
a pathological condition characterized by a decrease in the hydrogen ion concentration of arterial blood; caused by an increase in the concentration of alkaline compounds, or by a decrease in the concentration of acidic compounds or carbon dioxide to the body fluids
Parents (1)
img abnormal blood pH regulation MP:0003027
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal blood pH regulation MP:0003027
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanWNK465266WNK lysine deficient protein kinase 4
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 10589691, MOUSE PHENOTYPE ID: MGI:104696
img Jax MP, Pubmed Id: 20399150, MOUSE PHENOTYPE ID: MGI:2442345
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 20219826, MOUSE PHENOTYPE ID: MGI:103150
img Jax MP, Pubmed Id: 22550170, MOUSE PHENOTYPE ID: MGI:1917097
HumanHIF1AN55662hypoxia inducible factor 1, alpha subunit inhibitor
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 22550170, MOUSE PHENOTYPE ID: MGI:1917097
img Jax MP, Pubmed Id: 20399150, MOUSE PHENOTYPE ID: MGI:2442345
img Jax MP, Pubmed Id: 20219826, MOUSE PHENOTYPE ID: MGI:103150
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 10589691, MOUSE PHENOTYPE ID: MGI:104696
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img Jax MP, Pubmed Id: 20219826, MOUSE PHENOTYPE ID: MGI:103150
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 22550170, MOUSE PHENOTYPE ID: MGI:1917097
img Jax MP, Pubmed Id: 10589691, MOUSE PHENOTYPE ID: MGI:104696
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 20399150, MOUSE PHENOTYPE ID: MGI:2442345
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img Jax MP, Pubmed Id: 22550170, MOUSE PHENOTYPE ID: MGI:1917097
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 10589691, MOUSE PHENOTYPE ID: MGI:104696
img Jax MP, Pubmed Id: 20219826, MOUSE PHENOTYPE ID: MGI:103150
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 20399150, MOUSE PHENOTYPE ID: MGI:2442345
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 20399150, MOUSE PHENOTYPE ID: MGI:2442345
img Jax MP, Pubmed Id: 21593186, MOUSE PHENOTYPE ID: MGI:2153465
img Jax MP, Pubmed Id: 22550170, MOUSE PHENOTYPE ID: MGI:1917097
img Jax MP, Pubmed Id: 10589691, MOUSE PHENOTYPE ID: MGI:104696
img Jax MP, Pubmed Id: 20219826, MOUSE PHENOTYPE ID: MGI:103150
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003028alkalosis0self