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Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating triiodothyronine level
Debug Stats
  • ### Total Build Time: 65 ms 18.799 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 414 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 297 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 204 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 1.032 KB
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.057 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.938 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=39 ms Completed: 39 ms rowSize= 11.553 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.181 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal circulating triiodothyronine level MP:0005476
Definition (1)
aberration in the blood concentration of a hormone synthesized and secreted by the thyroid that is the main thyroid hormone used by the tissues
Synonyms (1)
"abnormal circulating level of triiodothyronine" EXACT
Parents (2)
img abnormal circulating hormone level MP:0005418
img abnormal triiodothyronine level MP:0005472
Children (2)
img increased circulating triiodothyronine level MP:0005480
img decreased circulating triiodothyronine level MP:0005479
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal circulating hormone level MP:0005418
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053767img abnormal triiodothyronine level MP:0005472
Genes (23)

Species:
human : 23
SpeciesGeneGeneIdGene NameEvidence
HumanARRDC357561arrestin domain containing 3
INFERRED
HumanNCOA18648nuclear receptor coactivator 1
INFERRED
HumanPAX87849paired box 8
INFERRED
HumanVIPR27434vasoactive intestinal peptide receptor 2
INFERRED
HumanUCP17350uncoupling protein 1 (mitochondrial, proton carrier)
INFERRED
HumanTTR7276transthyretin
INFERRED
HumanTSHR7253thyroid stimulating hormone receptor
INFERRED
HumanTHRB7068thyroid hormone receptor, beta
INFERRED
HumanTHRA7067thyroid hormone receptor, alpha
INFERRED
HumanTG7038thyroglobulin
INFERRED
HumanSSFA26744sperm specific antigen 2
INFERRED
HumanSLC16A26567solute carrier family 16, member 2 (thyroid hormone transporter)
img Jax MP, Pubmed Id: 16709608, MOUSE PHENOTYPE ID: MGI:1203732
HumanPTEN5728phosphatase and tensin homolog
INFERRED
HumanMAPK85599mitogen-activated protein kinase 8
INFERRED
HumanMED15469mediator complex subunit 1
INFERRED
HumanGPD22820glycerol-3-phosphate dehydrogenase 2 (mitochondrial)
INFERRED
HumanGHR2690growth hormone receptor
INFERRED
HumanFRK2444fyn-related kinase
INFERRED
HumanDIO31735deiodinase, iodothyronine, type III
INFERRED
HumanDIO11733deiodinase, iodothyronine, type I
INFERRED
HumanCRYM1428crystallin, mu
INFERRED
HumanCPE1363carboxypeptidase E
INFERRED
HumanAGRP181agouti related protein homolog (mouse)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005476abnormal circulating triiodothyronine level0self