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Details
Link-It Detail - Jax Mouse Phenotype - abnormal retinol metabolism
Debug Stats
  • ### Total Build Time: 14 ms 22.805 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 296 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 188 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=3 ms Completed: 3 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 18.488 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal retinol metabolism MP:0005444
Definition (1)
altered ability to metabolize retinol, which plays an essential role in metabolic functioning of the retina, and growth of and differentiation
Synonyms (1)
"abnormal vitamin A1 metabolism" EXACT
Parents (1)
img abnormal vitamin A metabolism MP:0011233
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal vitamin A metabolism MP:0011233
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanTTR7276transthyretin
img Jax MP, Pubmed Id: 10402668
img Jax MP, Pubmed Id: 12027900
img Jax MP, Pubmed Id: 11836246
img Jax MP, Pubmed Id: 11836246, MOUSE PHENOTYPE ID: MGI:87921
img Jax MP, Pubmed Id: 12851412
img Jax MP, Pubmed Id: 10358022
img Jax MP, Pubmed Id: 11836246, MOUSE PHENOTYPE ID: MGI:87921
img Jax MP, Pubmed Id: 10487743, MOUSE PHENOTYPE ID: MGI:97876
img Jax MP, Pubmed Id: 8384721, MOUSE PHENOTYPE ID: MGI:98865
HumanRBP15947retinol binding protein 1, cellular
img Jax MP, Pubmed Id: 12851412
img Jax MP, Pubmed Id: 11836246, MOUSE PHENOTYPE ID: MGI:87921
img Jax MP, Pubmed Id: 10358022
img Jax MP, Pubmed Id: 11836246, MOUSE PHENOTYPE ID: MGI:87921
img Jax MP, Pubmed Id: 11836246
img Jax MP, Pubmed Id: 8384721, MOUSE PHENOTYPE ID: MGI:98865
img Jax MP, Pubmed Id: 10402668
img Jax MP, Pubmed Id: 12027900
img Jax MP, Pubmed Id: 10487743, MOUSE PHENOTYPE ID: MGI:97876
HumanADH1C126alcohol dehydrogenase 1C (class I), gamma polypeptide
img Jax MP, Pubmed Id: 10402668
img Jax MP, Pubmed Id: 11836246, MOUSE PHENOTYPE ID: MGI:87921
img Jax MP, Pubmed Id: 11836246
img Jax MP, Pubmed Id: 10358022
img Jax MP, Pubmed Id: 10487743, MOUSE PHENOTYPE ID: MGI:97876
img Jax MP, Pubmed Id: 8384721, MOUSE PHENOTYPE ID: MGI:98865
img Jax MP, Pubmed Id: 12851412
img Jax MP, Pubmed Id: 12027900
img Jax MP, Pubmed Id: 11836246, MOUSE PHENOTYPE ID: MGI:87921
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005444abnormal retinol metabolism0self