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Details
Link-It Detail - Jax Mouse Phenotype - acidosis
Debug Stats
  • ### Total Build Time: 75 ms 15.920 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.582 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=64 ms Completed: 64 ms rowSize= 11.727 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
acidosis MP:0003031
Definition (1)
a pathological state characterized by an increase in the hydrogen ion concentration of arterial blood; caused by an decrease in the concentration of alkaline compounds, or by a increase 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 (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanWNK465266WNK lysine deficient protein kinase 4
Click here to display 32 evidence detail records.
HumanTMEM38B55151transmembrane protein 38B
Click here to display 32 evidence detail records.
HumanRHCG51458Rh family, C glycoprotein
Click here to display 32 evidence detail records.
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
Click here to display 32 evidence detail records.
HumanSLC4A48671solute carrier family 4 (sodium bicarbonate cotransporter), member 4
Click here to display 32 evidence detail records.
HumanSOD26648superoxide dismutase 2, mitochondrial
Click here to display 32 evidence detail records.
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
Click here to display 32 evidence detail records.
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
Click here to display 32 evidence detail records.
HumanREN5972renin
Click here to display 32 evidence detail records.
HumanPTEN5728phosphatase and tensin homolog
Click here to display 32 evidence detail records.
HumanOXCT150193-oxoacid CoA transferase 1
Click here to display 32 evidence detail records.
HumanNOS14842nitric oxide synthase 1 (neuronal)
Click here to display 32 evidence detail records.
HumanND64541NADH dehydrogenase, subunit 6 (complex I)
Click here to display 32 evidence detail records.
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
Click here to display 32 evidence detail records.
HumanHBB3043hemoglobin, beta
Click here to display 32 evidence detail records.
HumanERCC12067excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence)
Click here to display 32 evidence detail records.
HumanDMBT11755deleted in malignant brain tumors 1
Click here to display 32 evidence detail records.
HumanCA2760carbonic anhydrase II
Click here to display 32 evidence detail records.
HumanATP6V1B1525ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
Click here to display 32 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003031acidosis0self