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Details
Link-It Detail - Jax Mouse Phenotype - abnormal corticosterone level
Debug Stats
  • ### Total Build Time: 245 ms 21.826 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 306 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 195 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.010 KB
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.045 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.916 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=232 ms Completed: 232 ms rowSize= 14.678 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal corticosterone level MP:0003963
Definition (1)
anomalous blood or tissue amount of an adrenocortical steroid that induces glycogen deposition and regulates sodium conservation and potassium secretion
Synonyms (1)
"abnormal adrenal corticosterone level" EXACT
Parents (2)
img abnormal hormone level MP:0003953
img abnormal lipid level MP:0001547
Children (2)
img abnormal urine corticosterone level MP:0011548
img abnormal circulating corticosterone level MP:0005345
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal hormone level MP:0003953
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal lipid level MP:0001547
Genes (71)

Species:
human : 71
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCRTC2200186CREB regulated transcription coactivator 2
INFERRED
HumanUCN290226urocortin 2
INFERRED
HumanACD65057adrenocortical dysplasia homolog (mouse)
Click here to display 18 evidence detail records.
HumanC12orf1060314chromosome 12 open reading frame 10
Click here to display 18 evidence detail records.
HumanDFNB3125861deafness, autosomal recessive 31
INFERRED
HumanNMU10874neuromedin U
INFERRED
HumanRAI110743retinoic acid induced 1
INFERRED
HumanSLC23A29962solute carrier family 23 (ascorbic acid transporter), member 2
INFERRED
HumanCLOCK9575clock circadian regulator
INFERRED
HumanGTF2IRD19569GTF2I repeat domain containing 1
INFERRED
HumanTBX199095T-box 19
INFERRED
HumanIFITM18519interferon induced transmembrane protein 1
INFERRED
HumanPLA2G108399phospholipase A2, group X
INFERRED
HumanWFS17466Wolfram syndrome 1 (wolframin)
INFERRED
HumanVGF7425VGF nerve growth factor inducible
INFERRED
HumanUCN7349urocortin
INFERRED
HumanTRAF37187TNF receptor-associated factor 3
INFERRED
HumanTLR27097toll-like receptor 2
INFERRED
HumanTGFB17040transforming growth factor, beta 1
INFERRED
HumanZEB16935zinc finger E-box binding homeobox 1
INFERRED
HumanTACR16869tachykinin receptor 1
INFERRED
HumanSTAT36774signal transducer and activator of transcription 3 (acute-phase response factor)
INFERRED
HumanSTAR6770steroidogenic acute regulatory protein
INFERRED
HumanSST6750somatostatin
INFERRED
HumanSLC18A26571solute carrier family 18 (vesicular monoamine transporter), member 2
Click here to display 18 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003963abnormal corticosterone level0self