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Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating bicarbonate level
Debug Stats
  • ### Total Build Time: 14 ms 11.412 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 310 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= 581 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.047 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.580 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 6.200 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal circulating bicarbonate level MP:0003015
Definition (1)
aberrant concentration of inorganic salts that contain the -HCO3 radical in the circulation, which are an important factor in regulating the pH of the blood
Parents (1)
img abnormal blood homeostasis MP:0009642
Children (2)
img decreased circulating bicarbonate level MP:0003017
img increased circulating bicarbonate level MP:0003016
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal blood homeostasis MP:0009642
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A7115111solute carrier family 26 (anion exchanger), member 7
INFERRED
HumanWNK465266WNK lysine deficient protein kinase 4
INFERRED
HumanSLC4A557835solute carrier family 4 (sodium bicarbonate cotransporter), member 5
INFERRED
HumanWWOX51741WW domain containing oxidoreductase
INFERRED
HumanSLC9A823315solute carrier family 9, subfamily A (NHE8, cation proton antiporter 8), member 8
INFERRED
HumanSLC4A48671solute carrier family 4 (sodium bicarbonate cotransporter), member 4
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
INFERRED
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
INFERRED
HumanDMBT11755deleted in malignant brain tumors 1
INFERRED
HumanCA2760carbonic anhydrase II
INFERRED
HumanATP6V1B1525ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003015abnormal circulating bicarbonate level0self