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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vitamin C level
Debug Stats
  • ### Total Build Time: 40 ms 46.138 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 294 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 577 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.576 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 41.848 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal vitamin C level MP:0011229
Definition (1)
any anomaly in the concentration of L-ascorbic acid (vitamin C), which is a common co-factor and has anti-oxidant activities in many species
Synonyms (1)
"abnormal ascorbic acid level" EXACT
Parents (1)
img abnormal vitamin level MP:0005400
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal vitamin level MP:0005400
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanAKR1A110327aldo-keto reductase family 1, member A1 (aldehyde reductase)
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353434
img Jax MP, Pubmed Id: 19733551
img Jax MP, Pubmed Id: 10639167, MOUSE PHENOTYPE ID: MGI:1353434
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353494
img Jax MP, Pubmed Id: 16585534
img Jax MP, Pubmed Id: 22155581, MOUSE PHENOTYPE ID: MGI:108024
img Jax MP, Pubmed Id: 22820017, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 22155581
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 19482009
img Jax MP, Pubmed Id: 11984597, MOUSE PHENOTYPE ID: MGI:1859682
HumanSLC23A19963solute carrier family 23 (ascorbic acid transporter), member 1
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353434
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353494
img Jax MP, Pubmed Id: 19733551
img Jax MP, Pubmed Id: 22820017, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 22155581, MOUSE PHENOTYPE ID: MGI:108024
img Jax MP, Pubmed Id: 22155581
img Jax MP, Pubmed Id: 11984597, MOUSE PHENOTYPE ID: MGI:1859682
img Jax MP, Pubmed Id: 16585534
img Jax MP, Pubmed Id: 19482009
img Jax MP, Pubmed Id: 10639167, MOUSE PHENOTYPE ID: MGI:1353434
HumanSLC23A29962solute carrier family 23 (ascorbic acid transporter), member 2
img Jax MP, Pubmed Id: 19482009
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 11984597, MOUSE PHENOTYPE ID: MGI:1859682
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353494
img Jax MP, Pubmed Id: 10639167, MOUSE PHENOTYPE ID: MGI:1353434
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353434
img Jax MP, Pubmed Id: 19733551
img Jax MP, Pubmed Id: 22820017, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 22155581, MOUSE PHENOTYPE ID: MGI:108024
img Jax MP, Pubmed Id: 22155581
img Jax MP, Pubmed Id: 16585534
HumanRGN9104regucalcin
img Jax MP, Pubmed Id: 10639167, MOUSE PHENOTYPE ID: MGI:1353434
img Jax MP, Pubmed Id: 19482009
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 22820017, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 22155581
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353434
img Jax MP, Pubmed Id: 11984597, MOUSE PHENOTYPE ID: MGI:1859682
img Jax MP, Pubmed Id: 19733551
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353494
img Jax MP, Pubmed Id: 22155581, MOUSE PHENOTYPE ID: MGI:108024
img Jax MP, Pubmed Id: 16585534
HumanAKR1B1231aldo-keto reductase family 1, member B1 (aldose reductase)
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 10639167, MOUSE PHENOTYPE ID: MGI:1353434
img Jax MP, Pubmed Id: 19733551
img Jax MP, Pubmed Id: 11984597, MOUSE PHENOTYPE ID: MGI:1859682
img Jax MP, Pubmed Id: 22155581, MOUSE PHENOTYPE ID: MGI:108024
img Jax MP, Pubmed Id: 22820017, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 22155581
img Jax MP, Pubmed Id: 16585534
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1929955
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353494
img Jax MP, Pubmed Id: 19482009
img Jax MP, Pubmed Id: 20410296, MOUSE PHENOTYPE ID: MGI:1353434
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011229abnormal vitamin C level0self