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Details
Link-It Detail - Jax Mouse Phenotype - abnormal pH regulation
Debug Stats
  • ### Total Build Time: 10 ms 30.037 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 372 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 375 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 575 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 585 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.574 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 25.296 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal pH regulation MP:0004043
Definition (1)
anomaly in the function of the buffer systems of the body in combination with the respiratory and renal systems that control the relative acidity or alkalinity of the body, as measured by the concentration of hydrogen ion
Parents (1)
img abnormal homeostasis MP:0001764
Children (1)
img abnormal blood pH regulation MP:0003027
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053764img abnormal homeostasis MP:0001764
Genes (31)

Species:
human : 31
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
HumanSLC4A1057282solute carrier family 4, sodium bicarbonate transporter, member 10
img Jax MP, Pubmed Id: 18165320, MOUSE PHENOTYPE ID: MGI:2150150
img Jax MP, Pubmed Id: 23028982, MOUSE PHENOTYPE ID: MGI:103285
img Jax MP, Pubmed Id: 18077606, MOUSE PHENOTYPE ID: MGI:2443878
img Jax MP, Pubmed Id: 16260723, MOUSE PHENOTYPE ID: MGI:1096574
img Jax MP, Pubmed Id: 16354689, MOUSE PHENOTYPE ID: MGI:109350
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
HumanSLC4A79497solute carrier family 4, sodium bicarbonate cotransporter, member 7
img Jax MP, Pubmed Id: 16354689, MOUSE PHENOTYPE ID: MGI:109350
img Jax MP, Pubmed Id: 18165320, MOUSE PHENOTYPE ID: MGI:2150150
img Jax MP, Pubmed Id: 18077606, MOUSE PHENOTYPE ID: MGI:2443878
img Jax MP, Pubmed Id: 16260723, MOUSE PHENOTYPE ID: MGI:1096574
img Jax MP, Pubmed Id: 23028982, MOUSE PHENOTYPE ID: MGI:103285
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
INFERRED
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
INFERRED
HumanSLC9A36550solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
INFERRED
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
INFERRED
HumanSLC4A36508solute carrier family 4 (anion exchanger), member 3
img Jax MP, Pubmed Id: 23028982, MOUSE PHENOTYPE ID: MGI:103285
img Jax MP, Pubmed Id: 18165320, MOUSE PHENOTYPE ID: MGI:2150150
img Jax MP, Pubmed Id: 16260723, MOUSE PHENOTYPE ID: MGI:1096574
img Jax MP, Pubmed Id: 18077606, MOUSE PHENOTYPE ID: MGI:2443878
img Jax MP, Pubmed Id: 16354689, MOUSE PHENOTYPE ID: MGI:109350
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
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004043abnormal pH regulation0self