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Details
Link-It Detail - Jax Mouse Phenotype - abnormal renal reabsorbtion
Debug Stats
  • ### Total Build Time: 28 ms 23.627 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 637 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 204 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=2 ms Completed: 2 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.884 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.578 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 16.094 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal renal reabsorbtion MP:0010107
Definition (1)
any anomaly in the two-step process beginning with the active or passive extraction of substances (such as water, glucose, oligopeptides, amino acids, sodium (Na+) and other ions) from the renal tubule fluid into the renal interstitium, and the subsequent transport of these substances out of the renal interstitium back into the bloodstream; reabsorbtion begins in the proximal convoluted tubules and continues in the loop of Henle, distal convoluted tubules, and collecting tubules
Synonyms (1)
"abnormal renal basolateral membrane transport" NARROW
Parents (1)
img abnormal kidney physiology MP:0002136
Children (6)
img abnormal renal calcium reabsorbtion MP:0010111
img abnormal renal phosphate reabsorbtion MP:0010110
img abnormal renal water reabsorbtion MP:0010108
img abnormal renal glucose reabsorption MP:0011447
img abnormal renal protein reabsorption MP:0011445
img abnormal renal sodium reabsorbtion MP:0010109
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img renal/urinary system phenotype MP:00053675img abnormal kidney physiology MP:0002136
Genes (33)

Species:
human : 33
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC6A18348932solute carrier family 6 (neutral amino acid transporter), member 18
Click here to display 18 evidence detail records.
HumanSLC5A10125206solute carrier family 5 (sodium/sugar cotransporter), member 10
Click here to display 18 evidence detail records.
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
Click here to display 18 evidence detail records.
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
INFERRED
HumanCLDN1610686claudin 16
Click here to display 18 evidence detail records.
HumanEBI310148Epstein-Barr virus induced 3
INFERRED
HumanCLDN29075claudin 2
Click here to display 18 evidence detail records.
HumanCLDN109071claudin 10
Click here to display 18 evidence detail records.
HumanSLC4A48671solute carrier family 4 (sodium bicarbonate cotransporter), member 4
Click here to display 18 evidence detail records.
HumanFGF238074fibroblast growth factor 23
INFERRED
HumanHNF1A6927HNF1 homeobox A
INFERRED
HumanSLC22A56584solute carrier family 22 (organic cation/carnitine transporter), member 5
Click here to display 18 evidence detail records.
HumanSLC34A16569solute carrier family 34 (type II sodium/phosphate contransporter), member 1
INFERRED
HumanSLC15A26565solute carrier family 15 (oligopeptide transporter), member 2
Click here to display 18 evidence detail records.
HumanSLC13A16561solute carrier family 13 (sodium/sulfate symporter), member 1
Click here to display 18 evidence detail records.
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
Click here to display 18 evidence detail records.
HumanSLC9A36550solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
Click here to display 18 evidence detail records.
HumanSLC5A26524solute carrier family 5 (sodium/glucose cotransporter), member 2
INFERRED
HumanSLC5A16523solute carrier family 5 (sodium/glucose cotransporter), member 1
INFERRED
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
INFERRED
HumanNPPA4878natriuretic peptide A
INFERRED
HumanNOS14842nitric oxide synthase 1 (neuronal)
Click here to display 18 evidence detail records.
HumanNR3C24306nuclear receptor subfamily 3, group C, member 2
INFERRED
HumanMEOX24223mesenchyme homeobox 2
Click here to display 18 evidence detail records.
HumanKCNK13775potassium channel, subfamily K, member 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010107abnormal renal reabsorbtion0self