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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vitamin B12 level
Debug Stats
  • ### Total Build Time: 24 ms 5.981 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 311 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 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=5 ms Completed: 5 ms rowSize= 577 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 1.576 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 1.673 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal vitamin B12 level MP:0011227
Definition (1)
any anomaly in the concentration of cobalamin (vitamin B12), a water-soluble vitamin characterized by possession of a corrin nucleus containing a cobalt atom
Synonyms (1)
"abnormal cobalamin 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 (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanMEOX24223mesenchyme homeobox 2
img Jax MP, Pubmed Id: 20798259, MOUSE PHENOTYPE ID: MGI:103219
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011227abnormal vitamin B12 level0self