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Details
Link-It Detail - Jax Mouse Phenotype - increased circulating ammonia level
Debug Stats
  • ### Total Build Time: 23 ms 12.427 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 284 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 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= 589 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.588 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 8.096 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
increased circulating ammonia level MP:0005309
Definition (1)
significantly elevated levels of ammonia or its compounds in blood; often associated with liver failure and hepatic encephalopathy
Synonyms (1)
"increased ammonia level" BROAD
Parents (1)
img abnormal circulating ammonia level MP:0005308
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal circulating ammonia level MP:0005308
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanNAGS162417N-acetylglutamate synthase
Click here to display 26 evidence detail records.
HumanSLC25A1310165solute carrier family 25 (aspartate/glutamate carrier), member 13
Click here to display 26 evidence detail records.
HumanSLC7A79056solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
Click here to display 26 evidence detail records.
HumanHNF1A6927HNF1 homeobox A
Click here to display 26 evidence detail records.
HumanSLC22A56584solute carrier family 22 (organic cation/carnitine transporter), member 5
Click here to display 26 evidence detail records.
HumanPCK15105phosphoenolpyruvate carboxykinase 1 (soluble)
Click here to display 26 evidence detail records.
HumanOTC5009ornithine carbamoyltransferase
Click here to display 26 evidence detail records.
HumanOAT4942ornithine aminotransferase
Click here to display 26 evidence detail records.
HumanCPS11373carbamoyl-phosphate synthase 1, mitochondrial
Click here to display 26 evidence detail records.
HumanBTD686biotinidase
Click here to display 26 evidence detail records.
HumanASS1445argininosuccinate synthase 1
Click here to display 26 evidence detail records.
HumanASL435argininosuccinate lyase
Click here to display 26 evidence detail records.
HumanARG1383arginase 1
Click here to display 26 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005309increased circulating ammonia level0self