Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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 water reabsorption
go back to main search page
Accession:MP:0010108 term browser browse the term
Definition:any anomaly in the process by which water is passively transported out of the renal tubules back into the bloodstream
Synonyms:exact_synonym: abnormal kidney water reabsorption;   abnormal nephron water absorption;   abnormal renal water absorption



show annotations for term's descendants           Sort by:
abnormal renal water reabsorption term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Adcy6 adenylate cyclase 6 IAGP MGI PMID:20466003 NCBI chr15:98,484,982...98,508,119
Ensembl chr15:98,487,854...98,507,957
JBrowse link
G Agtr1a angiotensin II receptor, type 1a IAGP MGI PMID:21459331 NCBI chr13:30,520,339...30,566,850
Ensembl chr13:30,520,424...30,566,850
JBrowse link
G Akr1b1 aldo-keto reductase family 1 member B IAGP MGI PMID:10913167 NCBI chr 6:34,280,865...34,294,424
Ensembl chr 6:34,279,369...34,294,413
JBrowse link
G Cldn2 claudin 2 IAGP MGI PMID:20385797 NCBI chr  X:138,701,552...138,712,135
Ensembl chr  X:138,701,577...138,712,135
JBrowse link
G Hprt1 hypoxanthine phosphoribosyltransferase 1 IAGP MGI PMID:21459331 NCBI chr  X:52,076,955...52,110,537
Ensembl chr  X:52,077,014...52,110,536
JBrowse link
G Nos1 nitric oxide synthase 1, neuronal IAGP MGI PMID:10966931 NCBI chr 5:118,004,904...118,096,905
Ensembl chr 5:117,919,097...118,096,905
JBrowse link
G Slc12a1 solute carrier family 12, member 1 IAGP MGI PMID:17215439 NCBI chr 2:124,994,430...125,071,922
Ensembl chr 2:124,994,425...125,071,922
JBrowse link
G Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 IAGP MGI PMID:9662405 NCBI chr13:74,234,374...74,317,561
Ensembl chr13:74,269,576...74,317,561
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 16725
    homeostasis/metabolism phenotype 7706
      abnormal homeostasis 6864
        abnormal fluid regulation 1025
          abnormal renal water reabsorption 8
Path 2
Term Annotations click to browse term
  mammalian phenotype 16725
    renal/urinary system phenotype 2078
      abnormal renal/urinary system physiology 918
        abnormal kidney physiology 535
          abnormal renal transport 28
            abnormal renal water transport 11
              abnormal renal water reabsorption 8
paths to the root