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Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating aspartate transaminase level
Debug Stats
  • ### Total Build Time: 36 ms 21.168 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 426 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 365 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 224 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.068 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.939 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 14.264 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.187 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal circulating aspartate transaminase level MP:0000203
Definition (1)
any anomaly in the concentration in the blood of the enzyme which catalyzes the reversible transfer of an amine group from l-glutamic acid to oxaloacetic acid, forming alpha-ketoglutaric acid and l-aspartic acid
Synonyms (1)
"abnormal circulating serum glutamic oxaloacetic transaminase level" EXACT
Parents (1)
img abnormal circulating enzyme level MP:0001570
Children (2)
img increased circulating aspartate transaminase level MP:0005343
img decreased circulating aspartate transaminase level MP:0005632
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal circulating enzyme level MP:0001570
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053767img abnormal circulating enzyme level MP:0001570
Genes (58)

Species:
human : 58
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanAQP11282679aquaporin 11
INFERRED
HumanSRXN1140809sulfiredoxin 1
INFERRED
HumanSLC5A10125206solute carrier family 5 (sodium/sugar cotransporter), member 10
INFERRED
HumanOMA1115209OMA1 zinc metallopeptidase
INFERRED
HumanUNC93B181622unc-93 homolog B1 (C. elegans)
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanPI4K2A55361phosphatidylinositol 4-kinase type 2 alpha
INFERRED
HumanUACA55075uveal autoantigen with coiled-coil domains and ankyrin repeats
INFERRED
HumanZDHHC1354503zinc finger, DHHC-type containing 13
INFERRED
HumanWWOX51741WW domain containing oxidoreductase
INFERRED
HumanIL2250616interleukin 22
INFERRED
HumanFBXL526234F-box and leucine-rich repeat protein 5
INFERRED
HumanZBTB2026137zinc finger and BTB domain containing 20
INFERRED
HumanRPL13A23521ribosomal protein L13a
INFERRED
HumanIQGAP210788IQ motif containing GTPase activating protein 2
INFERRED
HumanBPNT1103803'(2'), 5'-bisphosphate nucleotidase 1
INFERRED
HumanZMPSTE2410269zinc metallopeptidase STE24
INFERRED
HumanNR1H310062nuclear receptor subfamily 1, group H, member 3
INFERRED
HumanDNM1L10059dynamin 1-like
INFERRED
HumanNR1H49971nuclear receptor subfamily 1, group H, member 4
INFERRED
HumanSQSTM18878sequestosome 1
INFERRED
HumanSTX118676syntaxin 11
INFERRED
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
INFERRED
HumanNR0B28431nuclear receptor subfamily 0, group B, member 2
INFERRED
HumanNR2C27182nuclear receptor subfamily 2, group C, member 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000203abnormal circulating aspartate transaminase level0self