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Details
Link-It Detail - Jax Mouse Phenotype - abnormal blood pH regulation
Debug Stats
  • ### Total Build Time: 35 ms 24.846 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 381 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=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 1.016 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.858 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.922 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 16.992 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal blood pH regulation MP:0003027
Definition (1)
anomaly in the function of the buffer systems of the blood in combination with the respiratory and renal systems that control the relative acidity or alkalinity of the blood, as measured by the concentration of the hydrogen ion
Parents (2)
img abnormal blood homeostasis MP:0009642
img abnormal pH regulation MP:0004043
Children (4)
img alkalemia MP:0003029
img alkalosis MP:0003028
img acidemia MP:0003030
img acidosis MP:0003031
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal blood homeostasis MP:0009642
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal pH regulation MP:0004043
Genes (27)

Species:
human : 27
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A7115111solute carrier family 26 (anion exchanger), member 7
INFERRED
HumanWNK465266WNK lysine deficient protein kinase 4
INFERRED
HumanHIF1AN55662hypoxia inducible factor 1, alpha subunit inhibitor
INFERRED
HumanTMEM38B55151transmembrane protein 38B
INFERRED
HumanRHCG51458Rh family, C glycoprotein
INFERRED
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
HumanPHOX2B8929paired-like homeobox 2b
INFERRED
HumanSLC4A48671solute carrier family 4 (sodium bicarbonate cotransporter), member 4
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanSOD26648superoxide dismutase 2, mitochondrial
img Jax MP, Pubmed Id: 9662405, MOUSE PHENOTYPE ID: MGI:105064
img Jax MP, Pubmed Id: 11677043, MOUSE PHENOTYPE ID: MGI:98352
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
INFERRED
HumanSLC9A36550solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
img Jax MP, Pubmed Id: 11677043, MOUSE PHENOTYPE ID: MGI:98352
img Jax MP, Pubmed Id: 9662405, MOUSE PHENOTYPE ID: MGI:105064
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
INFERRED
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
INFERRED
HumanRYR16261ryanodine receptor 1 (skeletal)
INFERRED
HumanREN5972renin
INFERRED
HumanPTEN5728phosphatase and tensin homolog
INFERRED
HumanOXCT150193-oxoacid CoA transferase 1
INFERRED
HumanNOS14842nitric oxide synthase 1 (neuronal)
INFERRED
HumanMUT4594methylmalonyl CoA mutase
INFERRED
HumanND64541NADH dehydrogenase, subunit 6 (complex I)
INFERRED
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
INFERRED
HumanHBB3043hemoglobin, beta
INFERRED
HumanERCC12067excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence)
INFERRED
HumanDMBT11755deleted in malignant brain tumors 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003027abnormal blood pH regulation0self