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Details
Link-It Detail - Human Phenotype - Abnormality of alanine metabolism
Debug Stats
  • ### Total Build Time: 15 ms 8.238 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 216 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 473 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 438 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.141 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 3.622 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of alanine metabolism HP:0010916
Definition (1)
An abnormality of an `alanine metabolic process` (GO:0006522).
Parents (1)
img Abnormality of pyruvate family amino acid metabolism HP:0010915
Children (1)
img Hyperalaninemia HP:0003348
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of pyruvate family amino acid metabolism HP:0010915
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of pyruvate family amino acid metabolism HP:0010915
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanMRPL311222mitochondrial ribosomal protein L3
img HP RolledUp, OMIM ID: 614582
HumanPDHX8050pyruvate dehydrogenase complex, component X
img HP RolledUp, OMIM ID: 245349
HumanPDHA15160pyruvate dehydrogenase (lipoamide) alpha 1
img HP RolledUp, OMIM ID: 312170
HumanPC5091pyruvate carboxylase
img HP RolledUp, OMIM ID: 266150
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010916Abnormality of alanine metabolism0self