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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vitamin absorption
Debug Stats
  • ### Total Build Time: 20 ms 20.859 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= 286 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=7 ms Completed: 7 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= 1.025 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.930 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 14.935 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 vitamin absorption MP:0001671
Definition (1)
any anomaly in the ability to take in any of a group of organic substances, present in food, that are essential to normal metabolism
Parents (2)
img abnormal intestinal absorption MP:0001666
img abnormal vitamin homeostasis MP:0004019
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053816img abnormal intestinal absorption MP:0001666
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal vitamin homeostasis MP:0004019
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanSLC23A19963solute carrier family 23 (ascorbic acid transporter), member 1
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 12138113, MOUSE PHENOTYPE ID: MGI:97877
img Jax MP, Pubmed Id: 23104561, MOUSE PHENOTYPE ID: MGI:2446957
img Jax MP, Pubmed Id: 19879271, MOUSE PHENOTYPE ID: MGI:1931307
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 12788952, MOUSE PHENOTYPE ID: MGI:99887
HumanRBP25948retinol binding protein 2, cellular
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 12138113, MOUSE PHENOTYPE ID: MGI:97877
img Jax MP, Pubmed Id: 23104561, MOUSE PHENOTYPE ID: MGI:2446957
img Jax MP, Pubmed Id: 12788952, MOUSE PHENOTYPE ID: MGI:99887
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 19879271, MOUSE PHENOTYPE ID: MGI:1931307
HumanPITPNA5306phosphatidylinositol transfer protein, alpha
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 19879271, MOUSE PHENOTYPE ID: MGI:1931307
img Jax MP, Pubmed Id: 12788952, MOUSE PHENOTYPE ID: MGI:99887
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 23104561, MOUSE PHENOTYPE ID: MGI:2446957
img Jax MP, Pubmed Id: 12138113, MOUSE PHENOTYPE ID: MGI:97877
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001671abnormal vitamin absorption0self