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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.
Term:abnormal renal reabsorption
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Accession:MP:0010107 term browser browse the term
Definition: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; reabsorption begins in the proximal convoluted tubules and continues in the loop of Henle, distal convoluted tubules, and collecting tubules
Synonyms:exact_synonym: abnormal kidney reabsorption;   abnormal kidney reuptake;   abnormal kidney uptake;   abnormal nephron absorption;   abnormal renal reuptake;   abnormal renal uptake
 narrow_synonym: abnormal renal basolateral membrane transport;   abnormal renal basolateral membrane uptake;   abnormal renal brush border transport;   abnormal renal brush border uptake
 xref: GO:0070293


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abnormal renal phosphate reabsorption term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ctns cystinosin, lysosomal cystine transporter IMP RGD PMID:35695380 RGD:155630629 NCBI chr10:57,801,551...57,817,213
Ensembl chr10:57,801,456...57,817,120 		JBrowse link
abnormal renal water reabsorption term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ugt1a1 UDP glucuronosyltransferase family 1 member A1 treatment IAGP RGD PMID:1127102 RGD:1354700 NCBI chr 9:88,801,344...88,808,465
Ensembl chr 9:88,713,184...88,808,465 		JBrowse link
G Ugt1a1j UDP glucuronosyltransferase family 1 member A1, jaundice mutant treatment IAGP RGD PMID:1127102 RGD:1354700
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  mammalian phenotype 5419
    renal/urinary system phenotype 649
      abnormal renal/urinary system physiology 478
        abnormal kidney physiology 142
          abnormal renal reabsorption 7
            abnormal renal calcium reabsorption 1
            abnormal renal glucose reabsorption 0
            abnormal renal phosphate reabsorption 1
            abnormal renal protein reabsorption + 0
            abnormal renal sodium reabsorption 2
            abnormal renal water reabsorption 3
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